3370 Biotech jobs

Are you a QC Analyst looking for an exciting opportunity? We are currently looking for a QC Analyst to join a leading pharmaceutical company based in the Kent area. As the QC Analyst you will be will be part of our quality control team and will provide testing activities (raw material identification and in process checks) that are required to support API GMP manufacturing. In addition, the ideal candidate will support the day to day running of the analytical equipment and support the internal chemistry teams with analytical chemistry techniques. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows: 1. You would be responsible for carrying out duties within QC laboratory, API manufacturing area and analytical lab, as well as preparing and testing samples from all phases of a manufacturing or other handling process (Raw material identification, in process testing, finish product analysis) under GMP regulations. 2. You will also be responsible for performing challenging analysis of raw and in-process materials, through use of a range of techniques: thermal analysis, HPLC, LCMS, GCMS, UPLC, SFC, NMR. This would include method development, optimisation and troubleshooting of the equipment. 3. Conduct all communication in a professional and positive manner. Provide regular updates to their manager and communicate openly in meetings. Listen to the opinions of the others and respond positively to feedback. 4. Preparing quality reports including analytical test reports and analytical specifications. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history: 1. The candidate requires a BSc/MSc/PhD in an analytical, chemical or related scientific field with demonstrated, relevant experience 2. Proven industry experience in GMP/GLP requirements associated with QC testing and API manufacturing, as well as detailed knowledge of chemical analytical techniques both theoretical and practical is essential for this position. 3. A working knowledge of Good Manufacturing Practice regulations and policies and equipment maintenance and troubleshooting skills. Key Words: Chemistry | QC | Quality Control | GMP | HPLC | LCMS | GCMS | UPLC | SFC | NMR | analytical | Pharmaceutical | Drug Discovery | API Manufacturing | Method Development Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

Technologist (Polymer /Organic/ Synthesis) c£33-50k +Benefits South East AB/J4408 An experienced PhD chemist with scale up or continuous flow experience (preferred) qualified is required to work very closely with R&D teams. As a PhD qualified organic or polymer chemist this a great opportunity to design and synthesise next generation materials for the business. There are also opportunities to influence multiple interfaces (like performance differentiation, Innovation, Manufacturing Technology, external outsourcing and Safety). The successful candidate will complement the R&D team's current skill base and play a critical role in enabling the team to become the High Performance Agile Team that deliver the new components the business needs (incremental, step-out & disruptive). This is a great role for an organic chemist who wants to be involved in Coaching - imparting experience and knowledge to a variety of skill bases and team members. Opportunity to build personal network extensively across range Influence our New Technology Innovation Culture. Greater understanding of market opportunities (short - long term) Exposure to Innovation & road map opportunities. Development of external outsourcing relationships. Influence lab set-up & equipment to support the synthesis needs of the business. Key Responsibilities Lead the scale-up from 10g to 10Kg with support from chemical engineer. Lead safety initiatives to continue to build on the strong safety culture, deliver risk assessments and consistently demonstrate the highest standards of safety and quality. Deliver robust routing scouting to deliver materials in a time efficient manner. Supervise, develop & coach laboratory based chemists. Prepare a variety of materials in an agile and efficient manner. External focal lead for assigned chemical outsourcing. Provide design solutions to a variety of programs to enable science teams to prove or disprove the working hypothesis. Communicate progress, challenges and delivery through a variety of communication media. Qualifications, Knowledge and Experience Required: PhD Chemistry, Polymer chemistry Synthetic Chemistry, Organic Chemistry, even pharmaceutical chemistry or a related petroleum subject. Technical background and commercial experience with things like 'scale up OR continuous flow chemistry or crude oil , Excellent organic chemistry background with strong track record of delivering materials to aggressive timescales within a research & development environment. Strong safety focus including networking, communication, a demonstrated ability to deliver high standard risk assessments, make solid safety recommendations when faced with obstacles and influence changes to work differently based on learnings from near miss reporting. Ability to take an objective view of technical problems and address them with creativity and innovation. Strong commitment to HSE and quality values They offer an attractive salary (dependent on experience), commensurate with qualifications and experience as well as associated benefits, including Bonus and Pension Scheme. To Apply: Please contact Alison Basson quoting AB/J4408 on

Here at Jet2.com and Jet2holidays the customer is VIP, we strive to exceed expectations. We work together as One Team in an Agile environment and we all drive a culture of change, inspiring and motivating each other to continuously improve current ways of working. We believe that our open and honest culture combined with great opportunities for learning makes Jet2.com and Jet2holidays a great place to work and leads to better service for our all-important customers. As a Front End Developer at Jet2.com & Jet2holidays , you will be responsible for building new and exciting user-centered developments and interpreting graphic visual or interaction designs in HTML, CSS, and JavaScript . In this exciting opportunity, you will build production-ready interfaces that work cross-platform for the Jet2.com and Jet2holidays websites. Experience building with HTML5/CSS and Javascript (ES6) is essential in the role. You'll be able to spot and fix cross-device/browser issues, including desktop, tablet, and mobile. Confident within an Agile environment, you will thrive on working as a team to deliver high quality, high traffic sites. The successful candidate will be a strong Front End Developer with a portfolio to prove it. With an increasing number of mobile visitors, you'll be experienced in building responsive mobile experiences. You'll be able to bridge the gap between design and technology, being able to think and speak the language of the UX designers and technical teams. Experience with SASS, Vue.js, Gulp, Webpack, and Git are desirable. You should be comfortable building components for CMS and have a deep understanding of usability and accessibility standards and approaches. Being a good communicator in this role is crucial. In return, we offer an excellent salary and benefits package with fantastic opportunities for progression in a growing business. This is a great opportunity to be part of an exciting forward thinking business. We operate scheduled leisure flights to holiday destinations in the Mediterranean, the Canary Islands and to European Leisure Cities from our 9 UK bases. Help us to send our all-important customers on holiday with Jet2.com and Jet2holidays !!

Strategy Consultant London, United Kingdom Salary up to £65,000 + Benefits This role is looking for someone who will drive improvements within business performance through Data and Analytics, you will be leading a small team and drive insight within the organisation. THE COMPANY This well top consultancy company is looking for a talented individual, to work with a team of experts on cutting edge projects that will change the business of the future. THE ROLE Lead a small team to operate as an internal consultancy that will enhance analytical innovations, work with the analytics manager to solve complex problems, help to make decisions and meet all business requirements, further details of the role are as follows; Manage and prioritise the analytics portfolio Create efficient business plans Make the most our of analytical resources Drive optimal business decisions Manage senior stakeholders in a confident manner Work on quantitative and qualitative scenario models prototype algorithms Maintain and share best practice Keep up to date with new ideas YOUR SKILLS AND EXPERIENCE Strong analytical skills Strong reporting skills Knowledge of reporting tools and techniques Strong Data manipulation Ability to solve business problems into a concise set of issues Good communication skills Strong project management skills Good knowledge of business problems T HE BENEFITS Earning potential up to £65,000 + Benefits HOW TO APPLY Please register your interest by sending your CV to Charlotte York via the apply link on this page

An excellent opportunity for a Biomedical Scientist (Band 6 or above) with experience with Laboratory IT systems looking to move into a customer focused role, offering product training, demonstrations and customer support for a global company with excellent market share. The role is field based with travel around the UK. This position is designed to assist our customer base by providing leading IT scientific support. The successful candidate should possess the passion and experience to deliver exceptional next generation application and hardware support both on-site and remotely. Your main duties in this position would include: -Customer Support, via the telephone -Installations -Customer training in-house and on customer sites -Attend all required company training -Maintaining good working relationships with customers -Ensuring a high level of service. Person specification: BSc Hons degree in Biomedical Science with experience working in a blood sciences laboratory. Experience with Laboratory IT systems (essential) Experience working in a remote customer support role (desirable) Experience troubleshooting & training Customer focused with excellent communication skills Our client is offering a fantastic remuneration package. Please get in touch for more details.

Sam Whyley-Smith is recruiting for a Senior Clinical Project Leader - Immuno-Oncology to join a long established and successful, niche Clinical Research Organisation focused in the Immuno-Oncology/Oncology area. This is a permanent position that will be fully home-based in the UK. Responsibilities: As a Senior Project Lead you will be responsible for planning, executing, supervising and managing large, global, complex, full service projects or multi-project programs across phases I-IV in Immuno-Oncology/Oncology. Key duties will include: Working alongside a team of experienced professionals, as well as individually you will be responsible for leading the planning and delivery of the effective implementation of clinical trials, whilst keeping abreast of project study trends, budgets, performance metrics and project reports. You'll provide an important point of control and assurance and therefore be required to maintain a high level of leadership and problem solving on complex projects; - Plan and execute multiple phase I-IV studies to agreed timelines, scope and budget. - Managing all aspects including overseeing vendors. - Ensuring patient safety, data integrity, and adherence to contract and protocols. - Playing a key role in bid defenses. Qualifications: - Substantial, proven experience as a Clinical Project Manager. - Therapeutic area experience in early phase oncology and immune-oncology. - Contract Research Organization (CRO) background. - Strong problem solving, organizational and time management skills. Ability to multi-task and attend to detail. - Strong and confident in bid defense. - Bachelor's or Master's degree. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47300 in all correspondence. CLINGEN

Leading international Pharmaceutical Manufacturer seeks experienced QC Release Officers. About the role: Reporting to the QC and Product Release Manager and to the Senior QC Release officer for day to day operational duties, the QC Release Officer is responsible for performing all necessary duties to comply with the quality system in place in accordance with cGMP and ISO standards. Ensuring the review of all batch documentation and subsequent product disposition is performed to comply with internal Standard Operating Procedures in accordance with the UK Quality System. Work in conjunction with production to ensure compliance status is maintained within the facility. Duties may include: Review of all pertinent batch documentation (including batch worksheets), as part of the product release process, in order to assess whether a product is compliant with a given specification and thus suitable for use ('fit-for-purpose' with regards to quality, safety and efficacy). Consideration must be given to any non-conformity raised during manufacturing Approval of individual batches for release to market or further internal use, once satisfied given specification has been complied with and all non-conformities have been considered with no impact on product quality. Support investigations of non-conformities that may impact upon the release process, product quality or compliance of the ASU facility to ensure manufactured products are compliant with specifications and suitable for its intended purpose. Support and lead the QC checker during normal shift operations to aid with resolution of any quality concerns. Contribute to the continuous improvement of all aspects of the quality system to ensure departmental objectives are met and compliance with regulatory requirements is consistently achieved for the ASU. Compilation of Certificates of Conformance as required to fulfil responsibilities to its customers. Operation of the Quality Assurance databases to support QA in publishing appropriate trends (e.g. KPI's) within the business. Where necessary, interfacing with other departments including attendance at meetings to ensure that the requirements of the QMS are met. Within the quality control and quality assurance team framework, to conduct additional duties as required to support colleagues in the effective execution of their duties. Ensure outsourced products are processed in a timely manner and made available for use with transactions performed on SAP (systems applications processes -stock management) updating status as required. The role holder must comply with policies or procedures relating to data privacy or information security. Participate in providing GMP training and coaching to staff. Support to the validation teams to ensure the principles of GMP are applied during validation activities. Generate and review departmental Standard Operating Procedures and associated worksheets. Perform the duties of QC checker when required. Deputise for the Senior QC Release Officer in day to day activities, when required. Skills and experience: Minimum of a Degree in a life science subject or appropriate experience of working in a quality assurance or control related function within either the pharmaceutical/ healthcare related industry for at least 5 years or within a relevant aseptic compounding industry for 3 years. Experience of aseptic operations is necessary; if possible aided by experience in aseptic compounding activities. Very good knowledge of GMP requirements specifically for manufacturing and control of aseptically produced products as laid down in the Orange Guide. Product knowledge. Attention to detail A demonstrable ability to communicate effectively, both verbally and in writing Organised and methodical work style Capability of leading small teams Computer literacy, competency in using Microsoft Office computerised systems and experience of using spreadsheets

Start Date: Immediate Kent Range 3-5 (depending on experience) We are looking to recruit a highly motivated ICT Technician who is looking to join our extremely successful Technical team. The successful candidate will work between the Primary and Secondary school sites. You will work alongside the Technical Support line manager and other experienced Technicians to deliver an efficient support service across the two schools. Ideally the successful candidate would already have experience of providing high quality technical support. It is envisaged that the successful applicant would be highly motivated, work well as part of a team, in addition to being extremely organised and thorough in their work. If you would like any further information or would like to arrange a tour of the school, please do not hesitate to get in contact with our Operations Manager, Mrs Lynn O'Neill. Closing Date: 21/02/2020 at 12:00 Interviews: To be arranged Information about the school St John's is a successful Catholic Comprehensive School with over 1100 pupils including c.250 in the Sixth Form. We have a very strong Catholic ethos and pride ourselves in being a warm and welcoming community. Many of our staff have been at the school for a very long time and we also have a number of staff who were actually students at St John's. Rebuilt in September 2010, St John's is a vibrant and progressive school offering outstanding facilities. This is an excellent and exciting time to join the school and be part of an enthusiastic, forward thinking and supportive team. Our exam results at both KS4 & KS5 are improving year on year. Our 2019 Progress 8 score of +0.40 is the fourth consecutive year of the school achieving a positive score on this key performance measure and a wonderful reflection of the talented and dedicated students and staff we have in the school. GCSE results exceed all targets with 60% of students achieving a grade 4+ in both English and Maths in 2019. If you would like to be part of this exciting opportunity, visit our website and click on the Information tab to locate Job Vacancies. Kindly complete the Application Form and Recruitment Monitoring Forms and email them to the address below. St John's is committed to safeguarding and promoting the welfare of children and young people and expects all staff and volunteers to share this commitment. Successful candidates will be required to undergo an enhanced DBS clearance. We regret that only shortlisted candidates will be contacted. Our School and all its personnel are committed to safeguarding and promoting the welfare of the children. This post is subject to an Enhanced Disclosure Application to the Disclosure and Barring Service. KTJ1

The Associate Scientist - Viral Vector Manufacture will work as part of an internal function for the generation and characterisation of viral vectors for both in-vitro and in-vivo applications (non-GMP). The appointee would work with Scientist and Senior Scientist colleagues to expand this service within the company. This function sits within the Viral Vector Manufacture Group, which addresses small scale (up to 500mL batches) production of lentiviral vectors, adeno-associated viral vectors (rAAVs) and adenoviral vectors. The appointee will work on commercial projects to deliver defined objectives, as well as on internal R&D projects to develop new technologies and platforms for future commercialisation. There will be frequent interactions and sometimes task sharing with Process Development group. Prior experience working in a laboratory environment is essential, as is familiarity with working to SOPs and producing batch records. Relevant techniques (see next section) include plasmid preparation, transfection (multiwell plates, hyperflask/stack, cell factories, suspension), harvest/clarification, characterisation by flow cytometry, qPCR, ELISA, Western blot. KEY RESPONSIBILITIES: - Work closely with internal and external stakeholders to define project goals and deliverables, in line the planned project objectives - Provide project summaries and reporting, as required - To adhere strictly to established quality standards, essential for on-going activities - Drafting and review of SOPs and batch records - Provide accurate record keeping at all times - Carrying out any other duties commensurate with the grading of the position, as required ESSENTIAL CRITERIA: - BSc or MSc in relevant discipline, with relevant laboratory experience (higher education qualifications with laboratory experience also considered) - Experience working in a commercial/industry environment is preferred but not essential - A high attention to detail - Ability to work in a laboratory independently and as part of a team on multiple projects, following established protocols, SOPs and safety procedures - Good time management, communication, teamwork and numeracy skills DESIRABLE CRITERIA: - Handling adherent cell lines in multiple formats (multiwell plates, hyperflasks/stacks, cell factories) - Experience in production and characterisation of viral vectors, and in implementation of best-practices for related processes - Handling and transfection of suspension cell lines - Optimisation and implementation of downstream processes for viral vectors - Analytical techniques for genetic characterisation of viral particles JOB LOCATION We have offices in the UK and USA. This role will be located at The Oxford Science Park, four miles south east of Oxford, with parking and good public transport links from Oxford. Our UK office address is: Oxford Genetics Ltd, Robert Robinson Avenue, The Oxford Science Park, Oxford, OX4 4HG. HOW TO APPLY Please apply online with your CV and let us know where you first saw the position advertised. Your CV should include evidence that demonstrates how you meet each of the selection criteria for the post using examples of your skills and experience. This may include experience gained in employment, education, or during career breaks. Your application will be judged on how you meet the selection criteria stated in the job description. Sending us your personal information means that you are asking us to hold your data on file, and understand that we will only keep it for as long as we need it to comply with the Data Protection Act. CLOSING DATE This advert will close as soon as sufficient applications have been received. Please submit your application as soon as possible to avoid missing the opportunity. INFORMATION FOR INTERNATIONAL CANDIDATES By the start of employment, the successful candidate must have, and be able to demonstrate, permission to work in the UK. Unfortunately, as a small company, we have very limited ability to sponsor employees under Tier 2 (General) of the points based system, and we are unable to sponsor Tier 2 work visas for international graduates / candidates. Company benefits OXGENE offers a generous benefits package: - 25 days annual leave, increasing to 30 with service and 8 UK bank/public holidays per annual leave year and a day off on your birthday - Pension with salary exchange and generous employer contribution - Group life cover - Glasses vouchers - Emloyee assistance programme - Business travel insurance - Private medical insurance with additional wellness benefits (as a benefit in kind) - Free tea, coffee, fruit-juice, fruit and biscuits, with kitchen facilities - Financially incentivised employee referral scheme - Free parking Company culture and environment OXGENE offers a friendly working environment in a diverse and expanding company. - Modern offices and laboratories - Opportunity to make a difference in a promotion-from-within environment - Regular whole-company presentations, including regular scientific updates - Regular social events, including TGI Friday activities - Annual two-day staff away days Salary: £20,000 - £28,000 per annum, dependent on experience plus benefits Simplified Recruitment is a Job Advertising Agency working on behalf of OXGENE. By applying for this position you are giving us permission to pass your CV and covering letter to a third party in relation to recruitment. A full copy of our privacy policy can be viewed on our website. Ref: SR506535

A returning client of mine in Addlestone are looking for an Administrator that has a passion for the world of Science. Working with a respected and large organisation, this is a great opportunity for candidates who are immediately available and looking to kick start a career within a Laboratory Technician role. This is a fixed term contract, starting ASAP and finishing approximately April 2020 - potentially longer. As part of the team your role will include maintaining laboratory equipment, set up of practical experiments, stock taking and ordering of resources and providing practical expertise whilst maintaining health and safety measures. My client are seeking an organised and enthusiastic individual with a passion for Science, a formal qualification in this area is desirable. The ideal candidate will have experience of working in a chemistry laboratory with an understanding of health and safety regulations and possess excellent communication skills and the ability to prioritise workloads. Monday to Friday, 08:30am - 16:30pm Salary £19,900 approximately, plus benefits.

Leading international Pharmaceutical Manufacturer seeks an experienced Microbiology Technician to join a talented team. About the role: To carry out environmental monitoring (EM) program of the aseptic compounding centre including; taking daily samples within production cleanroom areas, incubation, plate reading and identification of isolates. Documentation and data-entry of all results, following good documentation practices. Conducting investigations into EM excursions and non-reconciliations, generation and communication of KPIs, trending reports and state-of-control of compounding centre. To provide ongoing product sterility assurance through sterility testing and media-fill programs, and processing samples for external testing. Conducting investigations into out of specification results. Duties will also include liaison with internal customers and external suppliers. Duties may include: Carry out environmental monitoring program Incubation of samples Reading of plates and liquid media and evaluation of results Species-level identification of isolates Investigating EM excursions and out of specification results Sample processing for external testing Sterility testing of finished products Documentation and data entry of all results Trending of results and report-writing Writing and review of procedures, protocols and records relating to job role Skills and experience: Good communication and report-writing skills Minimum Degree Microbiology/related Science or relevant experience. Previous experience in working within a laboratory or pharmaceutical, microbiology or healthcare industries would be beneficial. The role holder is expected to work with minimal supervision against the agreed work programme; including work within clean areas.

Required from April 2020 (with possibility of part time from February 2020) Physics Technician (37½ hours per week, term time plus 2 weeks of holiday time - 36 weeks in total) To coordinate the use of practical resources and facilities and provide assistance and advice in meeting the practical needs of the Science curriculum, including liaising with all areas of the School and outside organisations. The successful applicant will have good ICT skills. Some electronics skills and previous relevant experience would be an advantage. Science is a thriving department where Physics is taught to A-level. A working knowledge of, or interest in, Physics would be an advantage as would the ability to support the Chemistry and Biology Departments. Salary based on Roedean NTS Points 20 - 24 (£21,366 - £24,152 per annum pro rata). Actual salary £16,723 - £18,903 per annum. Roedean is committed to safeguarding and promoting the welfare of children and young people and expects all staff and volunteers to share this commitment. An enhanced DBS check is required for all successful applicants. Please download an application pack from our website via the button below or contact Louisa Butler via email or . Closing date: 9am, 7 February 2020. Due to the need to appoint quickly we reserve the right to interview and appoint at any time.

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPLYING TO THIS CAREER OPPORTUNITY Senior Consultant or Managing Consultant - environmental policy London, Plymouth or Brussels Who we are: ICF ( ) is a global consultancy firm. In Europe, we have offices in the UK (London, Plymouth, Birmingham) and Belgium (Brussels). Our core business is to help governments, regulators and international institutions solve complex problems. We offer critical insight and rigorous analytical techniques to deliver innovative solutions and thought-provoking analyses for our clients. Working at ICF means applying a passion for meaningful work with intellectual rigor to help solve the leading issues of our day. Smart, compassionate, innovative and committed ICF employees tackle unprecedented challenges to assist our clients and benefit their constituencies. We believe in collaboration, mutual respect, open communication and opportunity for growth. Who we're looking for: We are looking for an experienced Senior Consultant or Managing Consultant to join a well-established practice within ICF that develops, analyses and evaluates environmental policies. The practice works extensively for the European Commission (e.g. DG Environment) and its agencies, as well as UK Government departments (e.g. Defra) and agencies. It tackles issues at the top of today's policy agenda, including biodiversity conservation, the marine environment, air quality, environmental governance and climate change. We are looking for an intellectually curious and very well organised individual, with an ability to see the many dimensions of a policy problem and to engage and work with leading thematic experts. Much of our work involves economic analysis and evaluation so skills in either area (and ideally both) would be a strong advantage. What you'll get to do: From day one, you will have the opportunity to win, manage and deliver a diverse range of projects for the European Commission and UK Government. You will deliver qualitative and quantitative research and analysis, including managing others' contributions and delivery. You will be a core part of our growing and collegiate team of like-minded analysts and project managers. You will work in an international environment in which more than 30 nationalities are represented. You will be contributing innovative ideas and practices to the business, helping achieve excellent, cutting edge research and expanding ICF's work into new areas. You will have the chance to develop your knowledge and skills further through excellent training and development opportunities. Your main responsibilities will be to: • Build relationships with our clients to understand and address their needs • Lead proposals, including building teams, developing methodologies and budgets • Oversee policy and/or economic research, analysis and evaluations • Manage project budgets, project teams including subcontractors, and the delivery of project outputs to a diverse range of clients • Deliver high quality research and analysis • Manage and develop junior members of the team • Pursue business development opportunities and build networks and partnerships What you'll need to succeed: You thrive in a fast-paced environment. You have a wide range of interests and are quick to develop a nuanced understanding of complex issues. You have a proven track record in contributing to impact assessments, evaluations and/or research projects. You are self-motivated, independent and able to manage a varied workload to deadlines without compromising quality. Your experience could have been gained delivering research work in government or a regulatory agency, the European Commission, academia, the private sector or the third sector. You will have: • Experience of a minimum of 5 years (Senior Consultant) or 8 years (Managing Consultant) • Expertise in environmental economics and/or evaluation of environmental policies and programmes, if possible including the application of innovative approaches to estimation of policy and programme impacts • Experience of managing large and complex projects / teams • Experience of writing competitive bids, managing budgets, tasks, and client interactions • Sound knowledge of EU marine, water and/or environmental policies • Ability to develop and convey expertise on a topic • Ability to think through the methodological challenges of investigating a topic • Good grasp of the strengths and weaknesses of qualitative and/or quantitative methods • Ability to write quickly and to communicate with others in excellent English (additional European languages would be an asset) • A relevant university degree

Blackfield Associates are currently supporting a leading Clinical/Medical Device Organisation in the search of a Quality Officer to be based Permanetly in the London office. You will be responsible for a number of operations supporting QA; Quality Management System, QA Operations, Information Privacy and Security. You will assist with the management of quality systems to ensure all computerised systems are maintained to GxP, ISO13485 rules and regulations. Working closley with the QMS Specialist to review, manitain quality policies/procedures. In addition you will perform due diligence and validation service/software product suppliers. The ideal candidate will have working experience of Quality Systems/Computer Systems Validation (CSV) strategies, ISO 13485 regulations and a good understanding of software within the Medical Device/Clinical industry. If you are interested in this opportunity then please send your CV to or call Craig on + STR Limited is acting as an Employment Agency in relation to this vacancy.

DATA ANALYST ST ALBANS 30,000 - 40,000 Do you have a curious mindset and the drive to want to explore and understand analytical problems? If you want to deliver insight for key business questions with a reputable company, then this could be the perfect role for you! THE COMPANY One of the UK's leading retail brands are growing their analytics function and looking to add a Data Analyst into the mix. With a great working culture, you will be able to add value to the overall successes of the business while sitting amongst a team of highly skilled analysts. THE ROLE As a Data Analyst you will be: Using SQL extract a wide range of data from multiple departments to identify key and actionable insights Involved cross-functionally to fully understand business queries to ensure best practices are achieved Delivering insight across to stakeholders to ensure the best methods and processes are in place Bringing in new ideas and opinions to add value into your team and the wider business YOUR SKILLS AND EXPERIENCE Confident user of SQL and Excel STEM background - 2.1 or higher Curious mindset Strong communication skills THE BENEFITS Pension scheme Healthcare Great working culture HOW TO APPLY Please register your interest by sending your CV to Gina Falleroni via the apply link on this page.

Laboratory/Manufacturing Technician - Neston/Cheshire 12 Month Contract Full Time (37.5 hrs/5 days per week) £13,000 - £17,500 pa Role as a Lab Technician for a period of 12 months. Working for a specialist scientific company, manufacturing Chromatography supplies, the role will involve routine laboratory work, including manufacturing and quality control testing and requires good attention to detail and manual dexterity. Full training will be provided Applicants should have a mature attitude, good communication skills and the ability to work unsupervised. Previous experience working in a laboratory or manufacturing environment, with a minimum GCSE science qualification is preferred but not essential. Although initially a 12 month contract, there is potential that this becomes a full time position. Generous 20 days paid holiday plus Bank Holidays Interested? Don't hesitate! Click "apply" now!

CK Group is recruiting for a Clinical Project Leader to join a company in the pharmaceutical industry at their site based in Leeds on a contract basis for 12 months and has a hourly rate of £24.94 PAYE / £32.76 Ltd. The Company: Our client is a multinational medical devices, pharmaceutical and consumer packaged goods manufacturing company who offer the worlds most comprehensive portfolio of orthopaedic and neuro products and services for joint reconstruction, trauma, spine, sports medicine, neuro, cranio-maxillofacial, power tools and biomaterials. The Location: The role is based at our client's state of the art R&D and production facility in Leeds. This site is a short distance from the M621 and is easily commutable on public transport as it is a short distance from Leeds city centre. The Role: This individual will be responsible for clinical project management within the company, as well as fostering strong, productive relationships with colleagues within the organization. Key Responsibilities: - Provide leadership within a clinical study, ensuring that each Team Member has a well-defined set of activities and objectives specific to their role and responsibilities within the context of their business focus. - Ensure efficient use of resources within the clinical study to provide high quality deliverables. - Manage all activities of assigned clinical studies within the Franchise Clinical Operations department. - Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders. - Understand business value and balance overall business objectives and functional needs. - May evaluate support requests for publications and provide consolidated comments and support to the requests. - May be involved in other tasks to support Clinical Operations and Operating Company as needed. - Manage Resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency. Your Background: - Minimum of a Bachelor's Degree, preferably in a Life Science, Physical Science, Nursing, or Biological Science. - BS with at least 3 years of relevant experience preferred. - Previous experience in clinical study management or equivalent is required. Relevant industry certifications preferred (i.e., CCRA, RAC, CDE). - Clinical/medical background a plus. - Medical device experience a plus. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47386 in all correspondence.

Reporting to the GM - Fatigue Safety , the Data Analyst (Fatigue) is responsible for assisting in the day to day management of the Jet2.com Fatigue Management System (FMS) by applying Human Factors principles to the Company Safety Management System (SMS) . Focusing on the data produced by the FMS, the Data Analyst (Fatigue) is required to source, manipulate, analyse and present relevant information that will enhance the management of fatigue within Jet2.com . Through the analysis of Fatigue Safety Reports and the assessment of incidents and near misses, you will support the collation of information to identify trends used by management for strategic decision making in the Fatigue Safety Action Group (FSAG) . You will promote the Jet2.com ' Just Culture ' and the anonymous, confidential reporting facility, in accordance with Company's Safety Management System. The successful candidate will preferably have experience working in an Airline Operations or Safety environment, and will therefore have a good understanding of operating a flying roster. You will have a strong knowledge of the aviation industry and will demonstrate a logical and analytical approach to problem solving. As the focal point for Crew Fatigue you will be approachable and empathetic whilst offering a high level of discretion and confidentiality. The Data Analyst (Fatigue) will also have excellent IT skills, particularly with MS Office applications and It would also be desirable if you are able to demonstrate experience of managing a database. In return, we offer an excellent salary and benefits package with fantastic opportunities for progression in a growing business. This is a great opportunity to be part of an exciting forward thinking business. We operate scheduled leisure flights to holiday destinations in the Mediterranean, the Canary Islands and to European Leisure Cities from our 9 UK bases . Help us to send our all-important customers on holiday with Jet2.com and Jet2holidays !!

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPLYING TO THIS CAREER OPPORTUNITY Role Profile: Port Ecologist Permanent contract (after a 12 month probationary period). Member of Port EHS Group reporting to the Chief Executive. Context • Dublin Port is the busiest port in the country with 16,500 annual vessel movements • The Port handles 88% of national Ro-Ro and 73% of national Lo-Lo traffic and approaching two-thirds of petroleum consumed in Ireland comes through the Port. • The basic infrastructure of the Port is upgraded and added to on the basis of Masterplan 2040 and it is envisaged that the Port will reach full capacity by 2040. • In addition to the objective of providing sufficient port capacity to cater for projected growth, Masterplan 2040 also has a core objective to re-integrate the Port with the City based on the Port's heritage and culture. • Dublin Port is located in the environmentally sensitive and protected area of Dublin Bay and is surrounded on the land side by densely populated urban and suburban communities. • DPC has committed in the Masterplan to develop and implement a Natural Capital policy as a means to achieving the sustainability of Port operations and development. • Port plans and projects are subject to detailed environmental analysis including SEA, EIA and AA and these require comprehensive, authoritative and lengthy data time series showing the condition and trends in habitats and species. • DPC actively engages with local communities and groups to tell the story of the Port to ensure that key stakeholders understand the Port's importance and relevance. Qualifications, experience & required skills/expertise • NFQ Level 8 (or equivalent) science qualification in a relevant area • Relevant Masters or doctoral qualification is desirable • Ten years' experience in researching, monitoring and managing habitats • An understanding and belief in the Natural Capital approach to compensate for the consumption of non-renewable resources and environmental degradation caused by port operations and development • A proven ability to enthusiastically and convincingly communicate verbally and in writing Baseline ecological data • It is essential that DPC understands, measures and reports on the condition of habitats and species of all types in Dublin Port and in areas contiguous to the Port (notably in the Dublin Bay Biosphere). • A comprehensive database of the condition and performance of habitats and species, particularly those with Natura 2000 protection, must be maintained and available for the preparation of reports needed for a variety of consent processes. Development of habitats • Port operations and construction works potentially impact the natural environment in a number of aspects including flora and fauna in the marine and terrestrial environments. These impacts need to be understood, measured and mitigated. • DPC must routinely create new habitats and increase biodiversity in Dublin Port and in areas contiguous to the Port (notably in the Dublin Bay Biosphere). Natural Capital • DPC has committed to developing a Natural Capital Policy • This policy must be relevant and bespoke to the Port's requirements while also remaining compatible with best practice elsewhere. • The degradation of the natural environment as a result of port operations and development must be recorded. • The consumption of non-renewable natural capital must be understood. • An appropriate level of natural capital must be created to offset degradation and consumption of non-renewables. Representation • DPC must be professionally represented in meetings with State / public bodies such as DCC, Dublin Bay Biosphere and the EPA and solid relationships developed and maintained. • Solid collaborative relationships must be maintained with organisations such as NPWS, BirdWatch Ireland, the Irish Whale and Dolphin Group, Coastwatch and the Irish Forum on Natural Capital. • DPC must work closely with universities and partake in and promote research. • DPC needs to be at the forefront in understanding the Natural Capital approach elsewhere both nationally and internationally (in the port sector) through participation and collaboration with environmental and port representative organisations such as ESPO. Communication • The condition and trends in habitats and species and of DPC's impact (positive and negative) on them must be communicated to a wide range of stakeholders including in an annual Sustainability Report. • Periodic scientifically robust and detailed reports on habitats and species are essential to ensure that the organisation gives appropriate focus in areas where problems are emerging. Consent process • It is essential comprehensive data is available for the preparation of environmental analysis for consent processes of various types. • The work of external experts in the preparation of applications for consents must be rigorously evaluated and challenged to ensure DPC maintains a robust and coherent approach to managing impact on the natural environment. TOP ACCOUNTABILITIES • Develop a coherent Natural Capital policy relevant to the circumstances of Dublin Port. • Monitor and measure the performance of habitats and species. • Devise and implement projects which increase biodiversity and increase the natural capital in the Port and in areas contiguous to the Port (notably in the Dublin Bay Biosphere) • Establish strong working relationships with State bodies, NGOs and universities. • Preparation of an annual Sustainability Report in collaboration with others. BARRIERS TO SUCCESS IN ROLE • DPC fails to develop a concise and coherent Natural Capital policy. • There is an evident diminution in biodiversity in the Port and in areas contiguous to the Port over time. • Trends in the conditions of habitats and species are not understood. • Projects to augment Natural Capital are not routinely designed and implemented. • Inability to work as part of collaborative multi-disciplinary teams. • DPC's commitment to protect and enhance the natural environment is not understood within the company or among key stakeholders.

Machine Learning Engineer London, United Kingdom Salary up to £75,000+ Benefits Want to work as a Machine Learning Engineer, solving cutting edge solutions and powering change through Data Science, sign up here! This is a chance to work on projects that will impact the real world and work towards transformations through Machine Learning. Working with one of the largest telecommunication businesses world wide, with access to vast amounts of Data. THE COMPANY This innovative company works with clients and organisations worldwide, join a collaborative team and work building ML and AI models to provide future solutions for clients.You will be responsible for industrialising Machine Learning models with large and varied data sets, the Machine Learning Engineer will create advanced end-to-end products to drive business value. THE ROLE Train Machine learning algorithms using pre trained models, using ML to provide platform success: Build transformer networks using pre-trained models Work with NLP Develop a platform that will operate worldwide Problem solve on a daily basis Analyse large data sets Lead projects within the ML Deploy fully functional models using ML models YOUR SKILLS AND EXPERIENCE Advanced degree in Machine Learning, Mathematics, Statistics Several work experience in ML PhD preferred Ability to lead projects Come up with innovative ideas Experience leading projects Experience leading a group of Machine Learning engineers SALARY AND BENEFITS Earning potential up to £65,000 + A number of benefits HOW TO APPLY Please register your interest by sending your CV to Charlotte York via the apply link on this page

Rob Walker is recruiting for a Process Chemist to join a metals and materials recycling company based in Derbyshire, on a full time, 6 month fixed term contract but may go permanent after that. This role would be suitable for candidates with a strong degree in Chemistry or a related discipline, excellent communication skills and the desire to succeed. As a Process Chemist, you will have responsibility for providing a high standard of analytical, scientific, environmental and process chemical support to the business. The role will support the Senior Chemist and take responsibility in their absence. You will also liaise closely with relevant departments and assist in matters related to the Company's environmental and quality performance. As a Process Chemist, you will have the following qualifications, skills and experience: - A proven track record of achievements. - A degree in Chemistry (or similar scientific field). - An ability to communicate with people at all levels in a professional manner. - A competence in Microsoft Office: Outlook, Word, Excel and PowerPoint. - The ability to work in a pro-active, accurate, efficient and timely manner. Further information about the Process Chemist role: - This role is an excellent opportunity for an outstanding candidate who is looking for a varied role with excellent career progression. - The ability to drive is an essential requirement as the site is not accessible on public transport. - Salary is dependent on experience with benefits including pension scheme, 25 days holiday plus statutory bank holidays, generous bonus scheme amongst others available on request. - Hours of work are 9.00 am - 5.00 pm (Monday - Thursday); 9.00 am - 4.30 pm (Friday); Lunch: 45 minute break each day. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47382 in all correspondence.

Have you built up experience in the quality control or testing of pharmaceutical or biochemical products? Do you have a good basis in method development of analytical platforms such as LC-MS or GC-MS? This Analytical Team Leader role is a great opportunity to join my client as they expand their laboratory management team due to a really impressive period of business growth. Your day to day duties as Analytical Team Leader will be: Developing methods on LC-MS, HPLC and GC platforms Conducting product analysis via GLP and GMP-compliant processes Leading a small team of analysts and bioanalysts Ensuring work supports a wider range of analytical and document-based studies A background in the following is required for the role: Experience in a relevant science-based industry A degree (or equivalent experience) in a chemistry field Knowledge of chemical testing, such as GC, HPLC, wet chemistry As I'd like to supply my client with a candidate shortlist ASAP, please apply immediately. For full consideration for this opportunity please apply with your CV (2 pages max., Word document format), plus your salary, location and eligibility to work in the UK details. Why would you work with Dr Paul Mears as your scientific specialist recruiter at Science Solutions? I focus solely on matching scientists to positions in the UK speciality chemical industry, which is where my own experience and network position me best given a background working in the speciality chemicals and fragrance and flavours sectors. I completed academic studies with a PhD in organic chemistry at the University of Manchester, which followed a BSc in the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up three years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.

Senior Data Scientist Consultant London, United Kingdom Salary up to £95,000 + Benefits Senior Data Science Consultant role just in, working in an ambitious environment, where you can use ML and AI to solve problems for future clients and tackle business problems. THE COMPANY Join this innovative management consultancy, this well established company is well known for its fantastic culture and exciting work environment. Join a team of Data scientists, to collaborate ideas, and work together on various interesting projects. This company offers career progression and access to large data sets. THE ROLE This role will allow you to improve your analytical skills; building models, improving modelling for architecture, and visualising the data to an expertise standard. Streamline processes Automate processes Interpret data for trends Propose new models Tackle business problems Problem solve on a daily basis Improve the modelling architecture Work with industry specialists YOUR SKILLS AND EXPERIENCE A degree or master's in computer science, Physics, Mathematics or similar Advanced SQL user Technically strong when handling data Experience with Data Visualisation; Power BI Understand of development process Understanding of version control Experience in web scraping SALARY AND BENEFITS Earning potential up to £65,000 + a number of benefits HOW TO APPLY Please register your interest by sending your CV to Charlotte York via the apply link on this page

DATA SCIENTIST £50,000-£75,000 + COMPETITIVE BENEFITS CENTRAL LONDON THE COMPANY: Our client is a very well-known telecommunications company which has a huge presence in both the UK and internationally. The company has a huge focus on technology and are leading the way with AI and Big Data. THE ROLE: You will be joining a team of highly skilled and likeminded Data Scientists and analysts where you will be contributing to complex and diverse projects to leverage Big Data and AI within the company which will result in measurable commercial benefit. In specific, you can expect to be involved in the following: Help to deliver complex and diverse projects with a commercial focus through the use of your in-depth knowledge in machine learning and statistical techniques. Implementing and optimising AI algorithms which can be replicated across several markets. Use hypothesis to discover relationships and patterns in complex data to provide commercial insight to the business. Use data visualisation to engage non-technical audience on a range of projects. YOUR SKILLS AND EXPERIENCE: The successful Senior Data Scientist will have the following skills and experience: Proven experience developing and implementing Machine Learning algorithms from large data sets which have helped to solve real world problems. Be experienced in mining large & very complex data sets using tools such as SQL, Hadoop, NoSQL and Spark. Have proven experience in using visualisation tools to create interactive dashboards which clearly communicate insight through tools such as Tableau, Power BI, Qlik etc. Have strong communication and interpersonal skills. Hold a Masters or Bachelor degree in a numerate discipline. THE BENEFITS: 28 days annual leave + public holidays Discounts across various big brands and services Private healthcare, childcare vouchers, retail vouchers and additional holiday options. Subsidised gym membership. Life assurance HOW TO APPLY: Please register your interest by sending your CV to Lillie via the Apply link on this page.

Data Science Manager London, United Kingdom Salary up to £80,000 + Benefits This is a consultancy company that aims to power action and create business value - the Data Science team being the ones who drive important decisions through Machine Learning and Artificial Intelligence THE COMPANY This company aims to focus on marketing outcomes addressing both he customers and clients needs. It is a start up that has been hugely successful since the creation, they are now looking for a talented Data Scientist to join the team. As a Data Scientist within this team you will have a huge impact in how the company will run and what this will mean for the Data and Analytics function. THE ROLE This role will allow you to drive forward and lead the Data Science function. You will lead projects and analytics, deciding what works best in the company. Further details of the role are as follows: Design analytical systems Deliver end-to-end Machine Learning models Work closely with clients Lead teams Produce market-leading outputs for clients Work across a number of diverse brands Focus on transforming the Data and Analytics function within the company YOUR SKILLS AND EXPERIENCE 5 years experience in a quantitative role Experience working with a consultancy desirable Previous experience with predictive models, Machine Learning, NLP and statistical modelling to solve business problems Strong technical skills Advanced R, Python and Alteryx user Experience of Data Visualisation tools Good communication skills BA in a quantitative subject Experience working across multi discipline teams Strong stakeholder management experience SALARY AND BENEFITS Up to £80,000 Private health and Dental care On site personal trainer Weekly football and yoga sessions Local discount cards Sabbatical after 5 years + Many other benefits HOW TO APPLY Please register your interest by sending your CV to Charlotte York via the apply link on this page

Computer Vision Engineer London, United Kingdom Salary up to £50,000 + Equity + unlimited holiday and flex working Are you an enthusiastic Computer Vision expert, who is willing to work on Machine Learning projects and looking for something more? Join this adventurous company that is exploring complex data to impact and provide solutions to new computer vision and advanced technologies. The aim of this company being to build new and exciting gaming opportunities. This company is looking for an engineer with strong interest in Computer Vision who can build technologies to be integrated into the iOS app. THE COMPANY Join a company and developers to look at the expansion of Artificial Intelligence and Computer Vision to produce breakthroughs through data transformation. Work with other Data Scientists in a collaborative environment, who are all keen to develop new ideas that impact the real world. THE ROLE This role will be an exciting opportunity to develop new solutions and work with Computer Vision and Artificial Intelligence. This role will allow you to solve complex roles on a daily basis and work with a variety of data, more details of the role are as follows: Using Computer Vision and Machine Learning to develop solutions -Working on an existing platform to develop the technology Problem solving on a daily basis Provide expertise when it comes to computer vision Work on data and projects to excite and please the audience Challenge and build on existing solutions Work with body tracking and face tracking Work closely with the CTO to prototype experiments YOUR SKILLS AND EXPERIENCE Enthusiastic problem solver Ability to lead and explore ideas with team Educated in a numeric discipline Deep understanding of Deep Learning Has knowledge of image segmentation Ability to work as a team and also independently Machine learning and Computer Vision experience Customer segmentation and Deep Learning experience Commercial experience and also experience using TensorFlow and PyTorch T HE BENEFITS Earning potential up to £50,000 + Benefits HOW TO APPLY Please register your interest by sending your CV to Charlotte York via the apply link on this page

Hyper Recruitment Solutions are currently looking for a Analytical Chemist to join a leading company based in the East Midlands area. As the Analytical Scientist you will be responsible for undertaking the chemical analysis of raw materials, intermediates and finished products according to set procedures and methods as well as preparing reagents, mobile phase and solutions according to set procedures and pharmacopoeial methods. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Analyst will be varied however the key duties and responsibilities are as follows: 1. Working as part of the Analytical team, you will be responsible for undertaking the chemical analysis of raw materials, intermediates and products according to set procedures and methods as well as preparing reagents, mobile phase and solutions according to set procedures and pharmacopoeial methods. 2. You will perform analytical testing using various techniques such as UV, IR, KF, HPLC, GC and dissolution analysis. 3. You will be responsible for the compilation of completed scientific documentation while maintaining accurate records of all work completed. 4. As the Analytical Scientist you will be a part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Analyst we are looking to identify the following on your profile and past history: 1. Relevant degree in a Chemistry or a Life Science subject with a significant chemistry portion. 2. Proven industry experience in a GMP laboratory environment. 3. A working knowledge and practical experience with analytical techniques (UV, IR, KF, HPLC, GC and dissolution analysis) Key Words: Analyst | GMP | Chemistry | HPLC Analytical | API | Raw materials Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.

The Sanger Institute have two exciting new opportunities for Software Developers to support the integration of an informatics pipelines within our sequencing informatics function. Working closely with other team members you will either add value to DNA Pipeline's data products, or reduce cost of producing existing data products (e.g. variant analysis). You will also aid in the development of systems to expose such data products and QC to scientist and their support teams. Key responsibilities are: Adapt and create tracking and QC systems (including visualisation). Help create, update and run analysis pipelines and their frameworks. Help ensure delivery and availability of products from such integrations Help ensure availability and use of QC metrics from such integrations Use "cloud" systems to provide these systems About you You will be experienced in amending and running analysis pipelines and have knowledge of at least one programming language suitable for computationally intensive algorithms. You will be comfortable working within a team environment but will also be responsible for you own workload with minimal supervision. Great interpersonal and communication skills is a must too as you will be working with customers to agree pipelines and work towards the continuous improvement of customer pipelines. Essential Skills Technical skillset Degree in bioinformatics, mathematics, physics or computer science or equivalent experience or software development experience. Experience of amending and running analysis pipelines. Contribution to bioinformatics, data analysis, tracking or visualisation tools. Knowledge of at least one programming language suitable for computationally intensive algorithms e.g. go, and of at least one language suitable for rapid prototyping or higher level orchestration. Comfortable using the shell, using or learning batch processing systems, and using or learning cloud compute. Competency skillset Willing to work both in an independent manner under minimal supervision, and also in a tight collaboration with other developers. Ability to work well within a team: keen to engage with tasks to help others, and to both take, assess and apply feedback from other team members, and to provide constructive feedback to others (most often by reviewing pull requests) Good communication skills. Other information To be considered for this role, please submit your CV and cover letter, detailing your experience and how you meet the criteria for this role. Closing Date: 26 January 2019 About Us The Wellcome Sanger Institute is a world leading genomics research centre. We undertake large-scale research that forms the foundations of knowledge in biology and medicine. Our findings are used to improve health and to understand life on Earth. Find out more on our website or follow us on social media. Our campus Set across 130 acres, just outside of Cambridge, The Sanger Institute is located on the stunning Wellcome Genome Campus. Home to some of the world's foremost institutes and organisations in genomics and computational biology, committed to delivering life-changing science with the reach, scale, and creativity to solve some of humanity's greatest challenges. Our benefits: There's an attractive benefits package on offer at the Genome Wellcome Campus. We appreciate the importance of achieving work-life balance and support this with a number of family and carer-friendly policies. Plus a flexible working policy for those who may wish to amend their working pattern or arrangement. As well as the usual benefits you would expect, we go much further: 25 days annual leave (extra 1 day to a maximum of 30 days for every year you work) Auto-enrolment into a generous Group Defined Contribution Pension Scheme, with enhanced company contribution Up to 2 days annual paid volunteering leave Up to 10 days paid Emergency Carers Leave per year Family friendly environment including options for flexible and part-time working, an on-site Workplace Nursery salary Sacrifice Schemes for pre-school children and Summer holiday club Life Assurance Cover and a Group Income Protection Scheme (if on a contract of 12 months or more) Enhanced maternity leave and parental leave Access to substantial number of courses and training events onsite Private Healthcare Scheme (after 6 months service) Eyecare and Dental payment plans Concessions and discounts from our corporate perks site Being part of the Genome Wellcome Campus you will be part of the beautiful working environment with an impressive range of benefits, services and facilities also including: Free bus service to and from Campus, covering various routes around Cambridge, Saffron Walden and surrounding villages A car-share initiative Free parking A number of on-site venues where you can meet, eat and socialise with colleagues A thriving Sports and Social Club which provides members with subsidised access to a gym, tennis courts, sports hall, fitness classes and a vibrant social calendar of events We hold an Athena SWAN Bronze Award and will consider all individuals without discrimination and are committed to creating an inclusive environment for all employees, where everyone can thrive.

We have an exciting new opportunity for a Senior Software Developer to support the integration of an informatics pipelines within our sequencing informatics function. Working closely with other team members you will design, drive and develop the integration of informatics pipelines which either add value to DNA Pipeline's data products, or reduce cost of producing existing data products (e.g. variant analysis). You will be experienced in creating, amending and running large scale sequencing analysis pipelines and long sequence read analyses to be able to deliver pipelines which work consistently to provide the data products. You will be comfortable working within a team environment but will also be responsible for you own workload with minimal supervision. Great interpersonal and communication skills is a must too as you will be working with customers to agree pipelines and work towards the continuous improvement of customer pipelines. Essential Skills Technical Skillset Degree in bioinformatics, mathematics, physics or computer science or equivalent experience. Experience of creating, amending and running large scale sequencing analysis pipelines. Experience of creating, amending and running long sequence read analyses. Creation or contribution to bioinformatics tools. Knowledge of at least one programming language suitable for compute intensive algorithms e.g. C, and of at least one language suitable for rapid prototyping or higher level orchestration. Comfortable using the shell, using batch processing systems, and using cloud compute. Competency Skillset Ability to work in an independent manner under minimal supervision - capable of day-to-day direction of one's own research. Ability to work well within a team: keen to engage with tasks to help others, and to both take, assess and apply feedback from other team members, and to provide constructive feedback to others (most often by reviewing pull requests). Good communication skills and experience of writing manuscripts for publication Other information To be considered for this role, please submit your CV and cover letter, detailing your experience and how you meet the criteria for this role. Closing Date: 26 January 2019 About Us The Wellcome Sanger Institute is a world leading genomics research centre. We undertake large-scale research that forms the foundations of knowledge in biology and medicine. Our findings are used to improve health and to understand life on Earth. Find out more on our website or follow us on social media. Our campus Set across 130 acres, just outside of Cambridge, The Sanger Institute is located on the stunning Wellcome Genome Campus. Home to some of the world's foremost institutes and organisations in genomics and computational biology, committed to delivering life-changing science with the reach, scale, and creativity to solve some of humanity's greatest challenges. Our benefits: There's an attractive benefits package on offer at the Genome Wellcome Campus. We appreciate the importance of achieving work-life balance and support this with a number of family and carer-friendly policies. Plus a flexible working policy for those who may wish to amend their working pattern or arrangement. As well as the usual benefits you would expect, we go much further: 25 days annual leave (extra 1 day to a maximum of 30 days for every year you work) Auto-enrolment into a generous Group Defined Contribution Pension Scheme, with enhanced company contribution Up to 2 days annual paid volunteering leave Up to 10 days paid Emergency Carers Leave per year Family friendly environment including options for flexible and part-time working, an on-site Workplace Nursery salary Sacrifice Schemes for pre-school children and Summer holiday club Life Assurance Cover and a Group Income Protection Scheme (if on a contract of 12 months or more) Enhanced maternity leave and parental leave Access to substantial number of courses and training events onsite Private Healthcare Scheme (after 6 months service) Eyecare and Dental payment plans Concessions and discounts from our corporate perks site Being part of the Genome Wellcome Campus you will be part of the beautiful working environment with an impressive range of benefits, services and facilities also including: Free bus service to and from Campus, covering various routes around Cambridge, Saffron Walden and surrounding villages A car-share initiative Free parking A number of on-site venues where you can meet, eat and socialise with colleagues A thriving Sports and Social Club which provides members with subsidised access to a gym, tennis courts, sports hall, fitness classes and a vibrant social calendar of events We hold an Athena SWAN Bronze Award and will consider all individuals without discrimination and are committed to creating an inclusive environment for all employees, where everyone can thrive.

The Company The BBI Group offers a portfolio of products and services to the diagnostic, healthcare, research, defence and food industries globally. Our mission is to deliver exceptional products and technologies that people rely on to enjoy a better quality of life. Through innovation, partnership, effective delivery and the collaboration of our people, we constantly strive to help set industry standards, engender trust and build our reputation for excellence. As a business, we are currently progressing through an exciting period of growth and as part of our exciting expansion plans, we currently have an opportunity to hire a QC Scientist for our BBI Solutions division. The role will be based at our Global Headquarters in Crumlin. BBI Solutions has served the global diagnostics industry for over 50 years, as a leading developer and manufacturer of raw materials and finished test platforms for the in-vitro diagnostics market. Benefits The salary offered for this role is competitive and makes up part of BBI's attractive benefits package, which includes: 5% contributory pension scheme Life Assurance Private health care scheme Generous annual leave package totalling 32 days (inclusive of bank holidays) Participation in the childcare voucher and cycle to work schemes The Role As the QC Scientist, you will perform in-process and final testing on the BBI Diagnostic product range, including rapid tests, liquid conjugates and gold colloid, ensuring that all QC activities comply with our quality standards (ISO 9001:2008, ISO 13485:2003 and the and the ANVISA RDC 16/13 regulations) Duties and responsibilities will include, but not be limited to the following: Carry out in-process and final tests to support manufacturing and R&D activities Carry out testing of incoming raw materials and record results on Incoming Data Sheets (IDSs) Carry out cross-over studies on new QC controls; also, stability testing at scheduled intervals Carry out quality monitoring and trending of the Purified Water System and record results on monitoring form Manage QC inventory Carry out release of conjugates using the Sage 200 ERP system Initiate required changes to QC documents in accordance with change control procedures; similarly, in conjunction with R&D, for new procedures to support product development Record and investigate out of specification and out of trend results; also, deviations Manage stability trials and perform testing at scheduled intervals Ensure that all interactions with Customers by self are professional Lead or participate in quality improvement opportunities within QC Ensure all activities comply with Health and Safety legislation or BBI policies Ensure that all QC activities comply with relevant standards and regulations The Person As the QC Scientist, you will need to have a science-based degree, laboratory experience and ideally be familiar with cGMP/ ISO 13485 and working within a regulated environment. Previous exposure to QC processes will be desirable. If you are an internal employee applying for this vacancy you and your manager are required to complete an internal transfer form. This needs to be completed in full and attached to your application along with your CV and cover letter.

CRYO PRODUCT MANAGER SUSSEX £45000PA THE COMPANY My scientific client was founded in 2001, its range of Thermo Instruments and electron microscopy (EM) products have expanded over the years. The company are proactive in responding to industry requests and requirements for new instruments and techniques. This first culminated in the introduction of the market-leading vacuum coating systems and cryo preparation systems for SEM and FIB/SEM - redesigns that have set the standard within the specimen preparation field. WHATS ON OFFER PENSION The company will match the personal level of contributions up to 5% of basic gross salary. LIFE ASSURANCE SCHEME Death in Service Life Assurance cover of 4 x annual basic salary is in operation. SHARE INCENTIVES CYCLE SCHEME THE JOB The role of the Cryo Product Specialist is a new position due to growth of the company. The successful candidate will be the ompany expert in cryogenic specimen preparation techniques. They will be able to demonstrate the capabilities of the cryo products and instruct users on the best methods of preparing a wide range of potential specimens. The role will require a deep understanding of low dose imaging and specimen freezing. THE PERFECT CANDIDATE Experience operating SEMs / FIBSEMs 5 years' experience in SEM / FIBSEM cryo specimen preparation and imaging. Cryo TEM experience would also be an advantage. Experience in the various methods of sample freezing and understanding of the limitations of each method. Proven record of providing applications training to customers Understanding of cryo workflow solutions and integration into different systems SAP Business 1 experience would be helpful Foreign language skills would be an advantage, especially Chinese / Japanese Must be willing to travel both within the UK and internationally up to 50% of time, in order to attend sales events, GET IN TOUCH Does this vacancy interest you? Contact Catherine Rynham for more details and full spec or

Hyper Recruitment Solutions are currently looking for a QC Validation Analyst to join a leading company based in the Cambridgeshire area. As the QC Validation you will be responsible for providing analytical support to a range of production processes and products. To actively contribute to the progression of ongoing process validation projects by conducting all aspects of analytical testing using a variety of analytical techniques. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Validation will be varied however the key duties and responsibilities are as follows: 1. As the QC Validation Analyst you will perform analytical work in support of validation projects that cover product process improvements, introduction of new material and equipment. You will be proficient with a variety of software and information systems. 2. You will complete analytical testing of pharmaceutical products using analytical equipment such as HPLC, KF, Dissolution, Particle Size. 3. As the QC Validation analyst you will maintain accurate written records and write reports in accordance with GMP/GLP. 4. You will work effectively across a multi-disciplinary team as well as keeping attention to detail, strong organisational, effective interpersonal and communication skills. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the QC Validation we are looking to identify the following on your profile and past history: 1. Relevant degree in Chemistry or similar scientific discipline. 2. Proven industry experience working in accordance with GMP/GLP as well as understanding of ICH guidelines, Pharmacopoeias and current regulatory expectations to ensure appropriate compliance within projects 3. A working knowledge and practical experience with a variety of analytical equipment; e.g. HPLC, KF, Dissolution, Particle Size. Key Words: QC, Quality Control, Validation, HPLC, ICH, GMP, GLP, Cambridgeshire, Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

Hyper Recruitment Solutions are currently looking for a Senior Analytical Chemist to join a leading Pharmaceutical company based in the Hertfordshire area. As the Senior Analytical Chemist you will be responsible for providing a range of analytical support to multiple project teams and work on API development. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Analytical Chemist will be varied however the key duties and responsibilities are as follows: 1. As the Senior Analytical Chemist you will take a lead role the development, optimization and validation of analytical methods working on API's, Intermediates, Starting Materials and Raw Materials within a GMP environment. 2. You will provide technical expertise across a range of analytical techniques including HPLC/UPLC, GC, MS and amoungst other spectroscopic techniques. 3. As the Senior Analytical Chemist your role will involve troubleshooting and maintenance of equipment and participate in instrument qualification. 4. You will write and review technical documents such as SOPs, protocols and reports, coach and mentor less experienced colleagues as well as review existing processes and provide input into continuous improvements. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Senior Analytical Chemist we are looking to identify the following on your profile and past history: 1. Relevant degree in a Chemistry related discipline. 2. Proven industry experience in analytical techniques such as HPLC and UPLC. 3. A working knowledge and practical experience with ICH guidelines and pharmacopoeias as well as working within a GMP and or GLP environment. Key Words: HPLC, UPLC, Senior Analyst, Senior Scientist, Analytical Development, Validation, Hertfordshire, South East. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

An exciting opportunity has arisen for a Senior E-Fate Study Director to join a successful and rapidly expanding scientific company. Are you confident conducting Environmental fate and/or metabolism studies in a GLP environment? Do you have extensive experience preparing study plans, updates and reports? Are you seeking a senior position with significant responsibility? Then this could be the role for you! You will act as Senior Study Manager/ Director for a range of complex studies in the Environmental area and ensure work is conducted within set timeframes and to the highest scientific and regulatory standards. Your responsibilities will also include training and mentoring of Study Directors/Managers, updates and reports as well as data review and QC checking. Successful applicants will have: Significant experience conducting E-fate/Metabolism studies in a regulated (GLP, OECD) environment Experience of study management or project management Excellent communication skills High attention to detail Previous people management experience is desirable but not essential NB: For the right candidate, our client is willing to provide visa sponsorship. ? Apply to VRS today to be considered for this rewarding opportunity! Keywords: Senior Study Director, Senior study manager, efate, e-fate, environmental fate, environmental, Chemist, Analyst, Analysis, Chemistry, environmental, soil, water, food, pharmaceutical, biological, sample analysis, GLP, GMP, GCP, OECD, good laboratory practice, Northamptonshire, Northampton, Huntingdon, Kettering, Midlands, VRS6073FP Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.

Senior Product Development Scientist Runcorn Permanent I am currently looking for 2x Senior Product Development Scientist to join a leading and expanding pharmaceutical company based in Runcorn. These are process based roles i.e. formulation and process development activities and statistical design of production processes. Your duties as the Senior Product Development Scientist will be varied however the key duties and responsibilities are as follows: * Responsible for project planning and resource planning along with costing of inhalation project activities * Responsible for management and reporting of inhalation product development programs, issuing regular updates to management and present appropriate project information * Design and complete product development studies in accordance with statistically designed experiments using DFM and QBD. Full understanding of pharmaceutical product development; understanding the analytical needs for drug product development. * Provide technical expertise for inhalation drug formulation and its analysis all to a cGMP standard. * Get involved in the investigation of out of specification/atypical results and the associated documentation, as well as CAPAs, change controls, procedural deviation management. * Frequently liaising with other departments such as QA and regulatory affairs in order to solve problems with documentation, regulatory filing, quality risk management and cGMP compliance. The Senior Product Development Scientist must have: * A BSc in a Chemistry or Pharmaceutical related field preferably with a formulation or process focus * Proven industry experience in formulation and analysis of drug products along with supervision or leadership of other staff members. * Skilled in dealing with the full life cycle of products, as well as project management and client interactions * A working knowledge and practical experience with HPLC, GC and method development and validation to ICH guidelines. If you are an experienced Senior Product Development Scientist looking for a new challenge please apply now! Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age.

Orion Group Sciences are looking for a Health Economics Senior Manager for our multinational pharmaceutical client based in the Middlesex area on an initial 10-month contract with the potential to extend. Job Purpose Orion Group are looking for a Health Economics Senior Manager, Economic Modeling COE - Mature and Late Phase Oncology. Leading core cost-effectiveness, budget impact and account calculator model development and adaptations to address local requirements, and being responsible for project management, content and execution in collaboration with cross-functional local, regional and global teams. Main Responsibilities of the role Developing the economic sections of HTA pricing and reimbursement submissions Providing input to Value Story development and updates Providing input to design and interpretation of evidence generation studies Interpreting clinical studies results and plan additional statistical analyses needed for core models and local model adaptations, including indirect treatment comparisons Presenting, discussing and re-analyzing model results Supporting timely and effective communication to HTA and reimbursement authorities Leading and supporting publications of core global and local economic models Managing a team of junior economic modelers Desired Experience and Background of the successful candidate Doctorate Degree and 2 years of health economics and outcomes research experience OR Master's Degree and 6 years of health economics and outcomes research experience OR Bachelor's Degree and 8 years of health economics and outcomes research experience Preferred Qualifications: MSc or PhD in Health Economics with a background in economics or in a quantitative field (such as statistics/biostatistics, epidemiology or engineering) 3+ years of experience in global health economics and outcomes research including US dossier submissions for coverage and reimbursement 3+ years of experience developing pharmacoeconomic models Experience working with consumers of outcomes information Knowledge of epidemiology, economics, psychometrics and medical writing Master and 6+ years, or PhD and 3+ years, of relevant work experience in the pharmaceutical industry, consultancy, academia or reimbursement agencies Previous experience in oncology Previous experience managing direct reports Strong experience in developing core and local adaptations of cost-effectiveness and budget impact models Strong statistical skills, in particular deep knowledge of advanced survival analyses Strong Excel skills and experience using Visual Basic, and software such as TreeAge Pro, R, SAS, Stata or WinBUGS for model development and data analysis Strong analytical and project management skills Strong verbal and written communication skills Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

The Company BBI Solutions has served the global diagnostics industry for over 50 years, as a leading developer and manufacturer of raw materials and finished test platforms for the in-vitro diagnostics market. Product ranges include antigens, antibodies, enzymes, serums and plasma's as well as renowned labels for lateral flow and ELISA assays. Our mission is to deliver exceptional products and technologies that people rely on to enjoy a better quality of life. Through innovation, partnership, effective delivery and the collaboration of our people, we constantly strive to help set industry standards, engender trust and build our reputation for excellence. We currently have an exciting opportunity for a Production Technician to join us on a permanent basis at our Sittingbourne site. Benefits The salary offered for this role is competitive and makes up part of BBI's attractive benefits package, which includes: 5% contributory pension scheme Life Assurance Private health care scheme Generous annual leave package totalling 32 days (inclusive of bank holidays) Cycle to work scheme The Role As an entry level Production Technician, you will be responsible for the manufacture and purification of proteins within the production team. We will provide full training and you will work closely alongside our experienced Production Scientists, reporting directly to our Production Team Leader. Duties and responsibilities of this role will include but are not limited to the following: To become competent in Production Protein manufacture without supervision as required Contemporaneous completion of quality records and batch records Preparation and use of columns, buffers and reagents Calibration and operation of key laboratory equipment Compliance with BBI's quality system requirements Completion of daily cleaning checks and records Responsible for maintaining individual training record Adherence to all SOPs, PSBRs, EOPs, SMPs and relevant documents Meet daily production targets Supporting production team members where necessary Requirements This role would be best suited to someone who has an interest in Biological/ Science. The successful candidate will be able to demonstrate excellent organisation skills, leadership qualities and an ability to work with multiple departments throughout the company. If you are an internal employee applying for this vacancy you and your manager are required to complete an internal transfer form. This needs to be completed in full and attached to your application along with your CV and cover letter.

Please note this role is part-time weekends and bank holidays The Team... The Professional Services Team works directly with GBG IDscan customers to resolve issues (technical or document related) reported by our customers. As a Professional Services Forensic Document Support, you will be the primary point of contact for GBG IDscan customers 24/7 who face a failed, suspect or unsupported document. The Role... Successful candidates will primarily support the FDE team by professionally assisting and validating various identification documents supplied by GBG IDscan customers. The Forensic Document Support will ensure customer support/queries are dealt with quickly and thoroughly across multiple platforms. As you build your document knowledge, you will help to maintain the IDscan document library. Intermittently, you may be asked to prepare reference data for our Document Knowledge Team to enable them to train our software and expand our samples database. What you will do... You will: •?Respond to customer requests over live chat, portals and emails. •?Reviewing semantic and visual features of identity documents day in and day out. • Manage daily transcript reports. •?Flexible attitude towards business hours and weekend will be required and will be scheduled on a shift basis. •?Managing document samples in a controlled careful and responsible manner as prescribed by IDscan. •?Regression test new document library packages and compare against older versions. •?If requested, help the document experts by preparing the required data for defining new document types or by enhancing the existing ones To be successful we are looking for... Skills: •?Data analysis and critical thinking skills. •?Ability to adapt and make decisions. •?Good communication skills, writing documentation skills and reporting, as well as an excellent command of the English language. •?Customer-focused individual with a drive to ensure customers have and continue to have a great experience when dealing with GBG. •?Fast learner for new tools, and IT systems. •?Baseline technical skills (Windows, Internet, Emailing, Microsoft office. Behaviours: • Supports others and recognises the importance of teamwork. • Shows evidence of clear analytical thinking. Eager to learn and determined to deliver excellent service to customers. • Ambitious with 'can-do' attitude. • Organised and able to work independently and on their own initiative •?Detail-conscious and committed to keeping accurate and up to date records Desired: •?Ability to collate information, analyse the data and come up with solutions to problems. •?Data/Information research skills. •?Basic Photoshop/Designing Skills knowledge. • University degree preferable. •?Knowledge about data protection and privacy. •?Knowledge about identity documents. • CIFAS Identity Document Fraud Training. Additionally... • Working hours: Sat: 8am-6pm Sun and Bank Holidays 11am-5pm • Our office is located on the Business park of Wilford Industrial Estate, Ruddington Lane, West Bridgford, Nottingham, NG11 7EP • convenient public transport • 23 days holiday/ pro rata plus additional Birthday holiday • pension scheme • optional private health care and more

CK Group is recruiting for a Senior Scientist to join a company in the pharmaceutical industry at their site based in Ware on a contract basis for 12 months and has a hourly rate of £14.17 PAYE. The Company: Our client is a global healthcare company who take on some of the world's biggest healthcare challenges. They provide health benefits to patients and consumers and have three world-leading businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products. The Location: This role is located on a state of the art R&D facility based in Ware, Hertfordshire. The town lies on the north-south A10 road which is partly shared with the east-west A414 (for Hertford to the west and Harlow to the east). Trains run from London Liverpool Street to Ware and take approximately 45 minutes. The Role: This role is for a laboratory based scientist to join and contribute to the capability & project research function of the Genetic Toxicology R&D group. Following appropriate training, the scientist will be expected to conduct research, collate and analyse experimental data, write scientific reports/summaries. They will also be expected to present the results of their work both internally or externally to the unit, as appropriate. Objectives for the role include: • Contribute to the evaluation of new technologies or to investigate issues associated with the risk assessment of genetic damage. • Involvement in general laboratory management duties throughout the year to support Discovery Support & Regulatory functions of the unit, as required • Timely and quality performance/reporting of studies • Transparency (access) of data and knowledge. Your Background: To be considered for this role you should have the following key skills, knowledge and experience: • BSc degree or equivalent in biology or related field • Demonstrated technical dexterity and experience in assay development • Excellent problem solving skills (flexible thinking) • Highly motivated with commitment to continuous improvement • Demonstrated scientific agility to balance multiple projects while maintaining highly focused attention to detail • Ability to work collaboratively in a matrix team environment and independently execute experiments • Excellent oral and written communication skills • Experience with Microsoft Office Suite Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47359 in all correspondence.

Pricing Data Scientist Reading £80,000-£90,000 I'm working exclusively with a unique data science team with the following core values: Analytical strength, curiosity and creativity - applying and developing Making an impact, FAST - fast-paced, start-up vibe Driving value - building impactful machine learning solutions to generate insights THE COMPANY This iconic fintech company is leading the digital age, who are keen to apply exploratory, potentially risky, data techniques to produce massive value! You will be joining a culture who are motivated by ambition, authenticity and creativity! Be a part of their young and exciting tech hub, working across all areas of the business using rich messy data sets. THE ROLE This is a completely Greenfield role where you will be working with senior management and stakeholders across all areas of the business. As a Data Scientist, you will be building machine learning solutions to roll out and add value to the business as a whole. Creating initial machine learning proof of concepts, in Python, Building and implementing these data solutions, using Python, to generate insights that will potentially save or make the company millions Effectively delivering technical concepts to non-technical management and stakeholders Researching cutting-edge machine learning techniques and applying these to commercial problems YOUR SKILLS AND EXPERIENCE Commercial experience using Python and its libraries, as well as AWS The successful Data Scientist will have proven commercial experience working with large, messy data sets to generate proofs of concept and building machine learning models in Python The ideal candidate will have commercial experience effectively delivering machine learning solutions to clients and will have led projects before Experience effectively communicating technical concepts to non-technical management and stakeholders is essential Preferred - experience implementing machine learning models, using Python, in a commercial role THE BENEFITS £80,000-£90,000 Healthy bonus Knowledge sharing/collaboration sessions Opportunities to take on mentoring and leadership responsibilities HOW TO APPLY Please register your interest by sending your CV to Kian Dixon via the Apply link on this page. For more information about similar roles, please get in touch!

PhD Qualified / Postdoctoral Chemist (Polymer /Organic/ Synthesis) c£30-50k +Benefits South East AB/J4408a An experienced Postdoctoral chemist with or without experience is required to work very closely with R&D teams. As a PhD chemist qualified in either organic synthesis, formulation or polymer chemist this a great opportunity to design and synthesise next generation materials for the business. There are also opportunities to influence multiple interfaces (like performance differentiation, Innovation, Manufacturing Technology, external outsourcing and Safety). The successful candidate will complement the R&D team's current skill base and play a critical role in enabling the team to become the High Performance Agile Team that deliver the new components the business needs. This is a great role for an organic chemist who wants to be involved in lots of different teams, is versatile and flexible. Coaching - imparting experience and knowledge to a variety of skill bases and team members. Opportunity to build personal network extensively across range Influence our New Technology Innovation Culture. Greater understanding of market opportunities (short - long term) Exposure to Innovation & road map opportunities. Influence lab set-up & equipment to support the synthesis needs of the business. Key Responsibilities - Roles will vary dependent on the specific team and their business priorities. Lead business critical technology projects and contribute to future project generation Be at the forefront of designing and developing our next generation of performance chemicals Organise, carry out and assess testing of chemicals performance and reliability to meet customer and internal requirements Present your reports on technical findings and give recommendations to key stakeholders that influence preferred outcomes Generate innovative solutions to formulation challenges. Design synthetic routes, prepare risk assessments, make novel chemicals and take molecules from concept to commercialisation Source complementary expertise externally and coordinate internal multifunctional teams Partner with customers to develop bespoke products Qualifications, Knowledge and Experience Required: PhD Chemistry, Polymer chemistry Synthetic Chemistry, Organic Chemistry, even pharmaceutical chemistry or a related petroleum subject. All background considered but preferences for synthesis OR formulation, R&D, scale up OR continuous flow chemistry. Excellent chemistry background with strong track record of delivering materials to aggressive timescales within a research & development environment. Strong safety focus including networking, communication, a demonstrated ability to deliver high standard risk assessments, make solid safety recommendations when faced with obstacles and influence changes to work differently based on learnings from near miss reporting. Ability to take an objective view of technical problems and address them with creativity and innovation. Strong commitment to HSE and quality values They offer an attractive salary (dependent on experience), commensurate with qualifications and experience as well as associated benefits, including Bonus and Pension Scheme. To Apply: Please contact Alison Basson quoting AB/J4408a on