1249 Biotech jobs

Due to expansion in workload and current business requirement, this highly successful and fast growing client based asbestos consultancy that offers a wide range of asbestos and environmental services to high profile clients currently requires the services of a skilled Asbestos Lab Analyst close to Sunderland and will include applications from Durham, Tynemouth, Newcastle and the surrounding areas. Qualifications & Experience: The applicant must have attained the P401 qualification and at the same time must have significant experience working within this role in a laboratory/office environment and within the asbestos field. Must have excellent communication skills, both written and verbal. Must have good organizational, client-facing and IT skills. Key Aspects of the Role: Receiving and preparing samples from site. Carrying out analysis of asbestos materials, etc., entering the results in LIMS and generating accurate data in line with standards - UKAS. Maintaining and developing UKAS accreditation systems. Maintaining and assisting quality control and data in an appropriate and accurate way and complying with the company's quality systems. Ensuring that all analytical equipment used are kept clean and up to date. Assisting and maintaining the company's the Quality Control system, etc. Liaising with clients and managers as and when required - dealing with issues effectively and appropriately. Solving problems pertaining to laboratory tests and making sure that the samples are stored appropriately or returned to the right place. Complying with the Health & Safety procedures. Getting involved with any other laboratory duties as and when required. In general, the successful applicant will be flexible, have good attention to detail and have the aptitude to work on own initiative and as part of a team. A fantastic salary depending on expertise and along with many other fringe benefits awaits the right candidate. Future Select are the leading market supplier for recruitment in the Asbestos industry, we work with the best clients & candidates and supply the majority of permanent jobs in the asbestos market. We have a large dedicated team, with over 25 years combined industry experience within Asbestos recruitment specifically geared to dealing with Asbestos Surveyors/Analysts/Lab Technicians, Administrators, Project/Regional /Technical/Quality/Training/Sales Managers through to Director level for both Consultancy & Removal. We have intrinsic knowledge of the marketplace, as well as respecting candidates/clients confidentiality in this close knit market sector. We are also interested in anyone with p401/p402/p403/p404/p404 or s301 CCP. We are inundated with applications, we will endeavour to get back in touch, however if you have applied to Future Select and you have not heard from us after a week, on this occasion, you will not have been successful. Your details will be saved on our system and you will be contacted in the future if a vacancy matches your skills. Future Select Copyright 2019.

Are you an experienced Research Scientist? Do you have expertise within Medicinal Chemistry? Are you looking for a challenging role within a state of the art facility? An exciting position has become available with our client who is a leading CRO. They are looking for a candidate to lead a team of Synthetic and Medicinal Chemists working on a range of projects covering a variety of therapeutic areas. Candidate requirements: PhD in organic or medicinal chemistry Significant experience within a CRO, pharmaceutical or Biotech organisation Excellent team working and communication skills A competitive salary and benefits package is available for the right candidate so 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.

Brigg Scientific are currently recruiting a QC Analytical Chemist for a well-established natural healthcare company based in the north-west. Working as part of a small QC analytical team in a fast-paced high-throughput laboratory you will be charged will conducting analysis using established analytical methods. Ideally possessing practical commercial experience a background in the pharmaceutical industry would be a distinct advantage. This role commands an annual salary of £22k. You will possess a BSc in Chemistry or a closely related subject and possess extensive experience of practical analytical chemistry with particular focus on HPLC from a GMP environment. Brigg Scientific is unable to employ any candidates requiring sponsorship to work in the UK and all applicants must be in a position to accept employment without infringement of their immigration status. Brigg Scientific is working as an Employment Agency in relation to this role. As part of the application process please provide GDPR consent via the Brigg Scientific website "Privacy Form" so we can hold your "personal data" and introduce you to future relevant employment opportunities.

The Christie NHS Foundation Trust, situated in South Manchester is the largest cancer treatment centre of its kind in Europe and an international leader in cancer research and development. On 12th October 2018 The Christie NHS Foundation Trust was once again rated as Outstanding by the health regulator becoming the first specialist trust in the country to be given their highest accolade twice. The Christie values diversity and is committed to ensuring equal opportunities for all and fair representation across the organisation at all levels. In support of these commitments, we welcome applications from Black, Asian and other ethnic minority people for this post. Radiotherapy Engineer Band 5 Would you like a fulfilling and meaningful career where all your hard work and effort goes towards helping cancer patients through their treatment? If so we'd like to hear from you. A number of fantastic opportunities have arisen at Band 5 at The Christie for enthusiastic and flexible service engineers to join our dynamic Radiotherapy Physics group. We are offering 2 positions in total one at each of our radiotherapy sites: in Withington and Oldham. The successful candidates will be educated to HNC level or higher with knowledge of electronic / electrical engineering, with a mechanical aptitude, and will join a team of specialist engineers providing a comprehensive repair, maintenance and development service to The Christie Radiotherapy department. We are looking for engineers with experience of working in healthcare or other industries such as Semiconductor Manufacturing, the Armed Forces, Radar Systems Engineers and other complex electromechanical system maintenance. You will ideally have/develop skills in the following areas: High power RF microwave and x-ray generation, vacuum systems, motor speed control, electronic position sensing and control, data acquisition and display, advanced digital imaging, laser alignment, medical computer systems, networking, and mechanical skills. Duties will involve quality control measurements, fault finding, repairs and planned maintenance of complex radiotherapy equipment, and other associated equipment e.g. MR / CT / Clinical Engineering Medical Devices. Manufacturer training will be provided where possible to enable individuals to work independently. Successful applicants will be supported to complete our comprehensive internal training program leading to registration as a Clinical Technologist with the Institute of Physics and Engineering in Medicine. The Christie NHS Foundation Trust, situated in South Manchester, is the largest cancer treatment centre of its kind in Europe, and an international leader in cancer research and development. The Christie provides a radiotherapy service to a population in excess of 3 million in the Greater Manchester and Cheshire area. In addition to the Withington site there are two operational radiotherapy satellite centres located in Oldham and Salford. These facilities provide local access to treatments for cancer patients. The centre at Salford also provides a stereotactic radiosurgery service. The Christie radiotherapy network has a total of 14 linear accelerators across the three sites. The Christie is the first centre in the country to offer High Energy Proton Beam Therapy. Other exciting developments include participating in the international MR linac consortium with The Christie set to be one of the first hospitals in the UK to offer MRI-guided radiotherapy. The closing date for this post may be extended if there are insufficient applicants or brought forward if there is a high volume of applicants. As users of the disability confident scheme, we guarantee to interview all disabled applicants who meet the minimum criteria for the vacancy All positions within the Christie are subject to the receipt of satisfactory written references, medical clearance, and evidence of your Right to Work in the UK. Some roles will require a Disclosure & Barring Service (DBS) check. Applicants invited to attend for interview will again be made aware of this at the point of invitation. Please note if you are successfully appointed to a post with this Trust, you will be required to pay for your own DBS Disclosure. If you have not heard from us within four weeks of the closing date, I regret that on this occasion your application will have been unsuccessful. The Inter-Authority Transfer (IAT) process is a critical and beneficial component of ESR and will form part of the recruitment process. In the event that you are successful following interview your previous NHS employment data, if applicable will be transferred from your current / most recent employer. Overseas candidates wishing to apply for this position and who would require immigration sponsorship, may wish to self-assess the likelihood of obtaining a Certificate of Sponsorship for the post on the UKBA website. For all staff employed after 1st June 2018, the contractual terms and conditions of employment make the flu vaccination a mandatory requirement. please see addiditional conformation sheet You should be aware the Trust operates a No Smoking Policy and therefore employees are not permitted to smoke at work. As an employer, The Trust values equality, diversity and inclusion. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

Great opportunity now available with a growing client of mine in Scotland. Having recently merged with another medical company, they are growing their presence in the global aortic and vascular implants market. Currently they manufacture a wide range of implantable devices and vascular products for the treatment of cardiovascular disease. Ultimately, the combined company will become a world leader in driving innovation and developing devices to treat aortic disease! Interested in being a part of this? Job Title: Supplier Quality Engineer Reference No: 250100 Location: Renfrewshire Job Type: Permanent Salary: £35k They're looking for a Supplier Quality Engineer to join on a permanent basis. You will be responsible for supporting the Engineering Leader to drive the team when it comes to monitoring supplier processes. You will be maintaining and consolidating a list of approved suppliers and ensure all related processes meet regulatory requirements. To be considered for this role you will need experience in Supplier management in a similar role within a regulated industry, ideally pharmaceutical or medical devices. Ideally you will have a degree in a scientific discipline as well as a Lead Assessor qualification. This client also offers a generous holiday entitlement as well as a pension and life assurance schemes to help safe-guard your future. There's also on-site parking and a subsidised on-site canteen. For more information on this position, please apply to Danni Arnold, Recruitment Consultant; ; . RHL is a specialist Recruitment Consultancy within Life Science talent acquisition. Recruitment Holdings Ltd (RHL) acts as an Employment Business and as an Employment Agency.

Our client are a Life Sciences business who have asked us to assist them in the search for a new Quality Manager to replace someone who is leaving after 20 years. REQUIREMENTS: - . A degree in Microbiology or Applied Biology (consideration would be given to applicants without a degree, if they have the relevant experience) . Experience of Food & Water Testing but not essential . Experience of ISO standards . Experience of audits and their requirements RESPONSIBILITIES: - . Day-to-day implementation of the quality system . Revisions and additions to the quality system in consultation with the Proprietor . Routine assessment of continuing competence of trainees and trained staff on a regular basis . Arranging and monitoring of internal and external QC samples and the production of trend analysis of the results . To ensure that all documentation relating to the quality system is completed, current and relevant to the system . Written preparation of methods and their validation . Review of source methods . Assisting the Proprietor and Laboratory Manger to ensure the laboratory is dealing with the workload, ensuring the production of accurate results . To perform any other duties reasonably allocated If you possess a suitable background and apply to me at I'll come back to you should I have any additional questions.

Great opportunity now available with a growing client of mine in Scotland. Having recently merged with another medical company, they are growing their presence in the global aortic and vascular implants market. Currently they manufacture a wide range of implantable devices and vascular products for the treatment of cardiovascular disease. Ultimately, the combined company will become a world leader in driving innovation and developing devices to treat aortic disease! Interested in being a part of this? Job Title: Quality Engineer Reference No: 248905 Location: Renfrewshire Job Type: Permanent Salary: £32k You will be responsible for Quality Engineering support to the complaints, including investigation and root cause analysis; review and analysis of returned complaint samples; complaint trend analysis and complaint reportability decisions. It's a part of the role to promote regulatory compliance, continuous improvement and high performance of the team. To be considered for this role, it is essential that you have experience of working within a quality role in a highly regulated environment, ideally medical devices or pharmaceutical. You should also understand regulatory standards and quality management systems. This client also offers a generous holiday entitlement as well as a pension and life assurance schemes to help safe-guard your future. There's also on-site parking and a subsidised on-site canteen. For more information on this position, please apply to Danni Arnold, Recruitment Consultant; ; . RHL is a specialist Recruitment Consultancy within Life Science talent acquisition. Recruitment Holdings Ltd (RHL) acts as an Employment Business and as an Employment Agency.

Our client a Global Biotech company, based in Speke is looking for a QA Associate to join their Quality team. This role is to start on the 6th January 2020 and to last for 6 months possibly longer. Key Responsibilities: The role holder will be a Quality member of the Fill/Finish (Secondary projects) project team, providing QA support for the delivery of an effective and compliant Fill/Finish operational facility. The role holder will be responsible for providing cGMP and quality support and guidance to the Secondary projects/operations and its support functions. The role will be required to perform QA Frontline duties during technical and qualification batches, including media simulations, and commercial batches once the Fill/Finish facility is commercially operational. The role holder will be responsible for QA review and approval of procedures, master batch records, and any other relevant cGMP documentation. They will also work as a member of cross-functional teams as defined by the Quality Assurance Manager. The role holder will also be required to provide QA support to the wider business, as and when required by the Quality Assurance Manager. The role holder must also confident in making frontline Quality decisions. Role requires making quality-based decisions; for example, those associated with batch records, deviations, validation activities. Work schedule prioritisation decisions are also required, and some decisions associated with training. Decision when to escalate issues associated with both these areas accordingly. Key Skills/Experience: Be able to liaise with QA team members, manufacturing teams and managers, laboratory supervisors, engineering representatives. Graduate in a relevant discipline, or able to demonstrate capabilities to this level. Have a good knowledge of cGMP requirements and applicable process knowledge. Experience working in a pharmaceutical environment. Experience working in Secondary (Fill/Finish) and/or aseptic operations (ideally). Understanding of EU and FDA regulatory requirements. General experience of Quality Management Systems. Competent IT skills, particularly MS Excel and Word. Possess good communication skills. Ability to work as a member of a team, but flexible to work on their own. Ability to manage multiple sets of information, prioritizing when required.

QA Associate Temp contract until July 2020 Day/Night Shift Competitive salary My client, a pharmaceutical company in Liverpool, are looking to appoint a QA Associate Responsibilities of the QA Associate include: * QA review and approval of procedures, master batch records, and any other relevant cGMP documentation. They will also work as a member of cross-functional teams as defined by the Quality Assurance Manager. * Review and approve procedures, master batch records, and any other technical or cGMP documentation in accordance with SOP, cGMP and license requirements. * Provide support for deviation investigations, ensuring effective root cause analysis investigations are performed and product quality implications accurately assessed. Identify repeat deviations and ensure appropriate corrective actions are taken. * Ensure that deviations, CAPAs, protocols/reports and other applicable documents are approved within the designated timelines. The ideal candidate for QA Associate must have: * A BSc or equivalent in a relevant discipline, or able to demonstrate capabilities to this level. * Previous cGMP experience * Experience of QA and QA Validation If you are an experienced QA Associate and happy to work shifts then 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

Reed Scientific are recruiting a Site Chemist for a growing chemical processing company in South Wales. Our client is a leading supplier of chemical management solutions; from manufacture through to disposal and embrace an ethos of internal promotion and investment in people. This role is ideal for someone with previous experience as a site chemist who is familiar with the chemical waste industry. The Role and Responsibilities: -Processing effluent and chemical waste. - Analyse water quality samples using a variety of inorganic chemistry techniques, including but not limited to colorimetry, ion chromatography, spectroscopy, titrations and wet chemistry. - Strictly adhere to the company's health and safety, environmental, procedural and statutory goals. -Adhere to relevant regulations, legislation and certifications and report results in a timely manner. -Working a rotational shift pattern, Monday to Friday, between 6am and 7pm. Desirable experience: -Previous experience in a "hand's on" Chemical Manufacturing or Effluent Management process beneficial. -Good Working knowledge of COSHH and Health & Safety. -Awareness of ISO 9001, 14001 & 18001 compliance regulations. Required: -A degree (or equivalent) in Chemistry or related subject area. -Proficient IT skills particularly with Microsoft Excel and/or similar database software. -Demonstrable Laboratory based experience using on Inorganic Chemistry techniques. -Practical, methodical and able to follow detailed written instructions with attention to detail. -Able to prioritise and plan workload.

We are currently looking for an Analytical Method Development Chemist for a growing pharmaceutical testing company in West Yorkshire. The company: Specialise in pharmaceutical analytical testing. They offer a highly technical analytical service for a range of Pharmaceutical and Biotech companies. The company focusses on troubleshooting, developing and validating analytical methods for a variety of pharmaceutical products. The role: As an Analytical Chemist you will perform analytical method development and validation activities for HPLC, GC, and IC, along with several detectors such as MS and MS/MS. Responsibilities include: Develop and validate methods for HPLC, GC, LC-MS and LC-MS/MS. Conduct analysis on a large range of samples including substances, compounds, formulations, final products and raw materials. Write and review documents relating to methods and protocols. Troubleshoot analytical methods and instrumentation. Ensure all equipment and instrumentation is well maintained and validated. Liaise directly with customers on projects providing timely updates on their progress. Ideal candidates: Will be degree or PhD qualified in Chemistry or Analytical Chemistry and have some experience working in a GMP or GLP environment. As an Analytical Method Development Chemist, you will have expertise in developing and validating HPLC or GC methods. Experience in LC-MS is desirable but not essential as training is provided. The company offers a competitive salary and benefits package with plenty of development and training opportunities! The role is commutable from north Manchester, Leeds, Harrogate, Bradford and Skipton Key words: Scientist, Analytical Chemist, HPLC, GC, Method Development, Validation, Pharmaceutical, GMP, GLP, chromatography, LC-MS

We are currently looking for a PhD Organic Chemist for a growing Pharmaceutical company in the South East. As an Organic Chemist, you will carry out complex Organic Synthesis to develop novel molecules for drug discovery and development projects. Duties include: Solve complex synthetic chemistry problems. Design and carry out experiments using several laboratory techniques. Develop synthetic routes and perform synthesis on target molecules/ drug candidates. Write and review technical reports and documentation. Ideal candidates will have a PhD in Organic Chemistry or Medicinal Chemistry. The position is open to recent PhDs or a Masters graduate with industrial experience in synthetic organic chemistry. This is growing company with some fantastic facilities. The company offers a highly competitive salary and benefits package. To apply please send your CV to Peter at Rowland Talent Solutions. Key words: Medicinal, Synthetic, Synthesis, Organic Chemist, Drug discovery, Drug development, Pharmaceutical, Chemistry, Senior Scientist

Graduate Teaching Assistant (Social Sciences) - Sheffield Are you a recent Social Sciences graduate considering a career in education? Working as a Graduate Teaching Assistant or Graduate Cover Supervisor is a great way to gain PAID experience in a secondary school environment before enrolling onto a PGCE, SCITT or similar Teacher Training Programme whilst earning money!..... click apply for full job details

Sales Manager - UK & Ireland This is a home based role - also an option to be based in Manchester Professional Hygiene / Personal Care / Home Care products - chemistry based Highly competitive salary, bonus & benefits and option of a car allowance or company car...... click apply for full job details

Senior Dimensional Calibration Engineer / Mechanical Calibration Team Leader / UKAS Signatory is required immediately for a permanent position in the Derby / Nottingham area. Competitive, negotiable salary (dependent on experience and qualifications) The Dimensional Calibration Engineer will be working circa 37 - 40 hours (Usually Mon - Fri Days) + occasional O/T...... click apply for full job details

IntaPeople are working with an exciting late stage start-up who are looking to hire a Senior Design Lead at their Cardiff office. They are on an exciting journey with a strong roadmap map ahead and are rapidly scaling their customer base across the world...... click apply for full job details

Based in the Edinburgh BioQuarter, the company offers specialist preclinical contract research services to Pharmaceutical & Biotech companies focused on Immuno-Oncology, Immunology, Neuroscience and specialised multiplex Histology. Job Description: They are looking for an experienced Senior Scientist, with skills in complex immunohistochemical and immunofluorescent staining, including multi-plex assay development (4-9 plex), in-situ hybridisation (RNAscope), and other molecular tissue probing techniques. The post holder will also use the Vectra Polaris for whole slide scanning and multispectral imaging, while also supporting data management activities. Key Tasks: Project Management - Working with the team and relevant academic contacts, as required, to ensure quality conduct and delivery of client projects. - Ensuring accurate record keeping of all experimental work, from initial protocol development, accurate lab notes, through to write up of results and report production, archiving. - Implementing quality control steps to ensure projects are conducted and delivered according to the standards expected (GCP), developing new or updating SOPs as required. - Line management of Scientists, delegation of project tasks across the team to ensure accurate and timely delivery of client data. - Communicating effectively with both clients and internal teams as required. Project Delivery/R&D - Actively interrogating scientific literature to understand relevant technical protocols and advances as necessary for driving forward bespoke client projects. - Independently perform complex fluorescent and colourimetric staining assays including multi-plex assay development (4-9 plex). Contribute to the development of improved methods and techniques including antibody validation and optimisation. Troubleshoot assays. - Design and perform RNAscope cell and tissue assays using robotic staining platforms (Leica Bond). Business Development - Taking an active role in nurturing new and expanding existing client relationships - May have opportunity to attend scientific and trade conferences to deliver oral presentations and posters and to attract new commercial opportunities. Desired Skills/Experience: - Life science degree (Biomedical Sciences/Biological Sciences), post-graduate degree an advantage and a minimum of 3 years relevant work experience. - Previous experience of Pharma/Biotech drug discovery or contract research desirable. - Demonstrable relevant laboratory experience. - Skills in image analysis would be of benefit. - Strong communication skills and teamwork ethic, highly motivated and entrepreneurial personality. They are looking to offer the position to a dynamic individual, who would be excited about the prospect of making a valuable scientific contribution to the future growth of the organisation.

Principal Bioinformatician Salary within the range of £31,334 - £41,224 per annum (depending upon experience) Job Ref: MI/19/72_2 Duration of post: Fixed term until 31 st March 2022 About the role: The overall goal of the Cancer Biomarker Centre (CBC) in the CRUK Manchester Institute led by Professor Caroline Dive CBE, is to develop, validate, and implement biomarkers that facilitate the optimisation of..... click apply for full job details

Microscopy Analyst - 12m FTC £17,000 - £18,350 Evesham Are you looking to develop a career within science? Our client is seeking someone with a passion for science to join their busy team on a contract basis. Working within a fast-paced department, you will be responsible for conducting microscopic investigations to support the resolution of customer complaints. This is an ideal role for someone looking to develop their practical skills in a professional environment. Duties include: Carrying out microscopic investigations of foreign bodies using a range of methods Interpret analytical data Preparing technical reports in an easily digestible style Maintain accurate records of results You will need to be: Educated to A Level or above Inquisitive Adaptable An excellent communicator A driver with own transport For immediate consideration, please send your CV to Recruitment today. We like to speak to every application, but due to the current climate this is not always possible. To ensure your application is not overlooked it is important that you emphasize any skills or work experience relevant to this position. If you have not heard from us within 5 working days please assume that you have been unsuccessful in this instance. i2i Search & Selection Ltd is an independent employment agency providing staffing solutions across specialist areas. We are dedicated to providing a professional quality of service to clients and candidates alike.

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.

Bioinformatics & clinical data management specialist for growing company in Cambridge, project leadership Your new company Is a rapidly growing pharmaceutical data & bioinformatics company in the Cambridge area, providing bespoke solutions to a range of clients within the pharmaceutical, biotech and genomics fields, using a range of pipelines, software and data analysis tools to make a big difference to their clients, working with multi-omics and clinical trial data sets to fast-track a range of programmes. The company has bright, well-equipped, open plan offices and a collaborative and warm corporate atmosphere. Your new role You will be joining an enthusiastic and talented team, taking on / leading data management and troubleshooting for clients on the company's software platform (which is focused on clinical trial, bioinformatics and drug discovery data analysis). For more experienced candidates there is scope to input into strategy and company development plans. The major responsibilities include: Downloading and loading biological or clinical data sets from/to public repositories and internal platforms; Providing training and ongoing support to internal teams and clients on data issues/queries; Scripting (either from scratch or optimising existing scripts); Data wrangling of large / diverse data sets; Providing customer and market feedback to internal development teams to identify market opportunities; Building relationships with clients for future business. This is a fast-paced environment where you will need to deal with people at all levels, from developers through to senior management/C-level executives. What you'll need to succeed As well as excellent analytical, organisational and team-working skills, you will need to have an innovative approach to problem solving and be able to work both independently and as part of a larger team. You should have a degree (or equivalent experience) in bioinformatics, computational biology, computer science, computational chemistry, physics, statistics, mathematics, biology, genetics or a related field. Experience with biological or clinical trial data, eg from hands-on analysis or as a data manager and/or genomics, drug discovery (eg assay or screening services) or bioinformatics would be a significant advantage. You will also need: A good understanding of pharmaceutical, clinical or similar research, from either academia or industry work experience; Good data wrangling skills, with scripting experience; Knowledge of biological or clinical data formats, eg VCF, FASTQ, BAM, SDTM, etc Hands-on experience with clinical trial or biological data systems / software (eg RAVE, Medidata or other EDCs), bioinformatics, drug discovery or similar software; Familiarity with data standards, such as CDISC; An aptitude for creative problem solving, especially within technical problems. Candidates with related experience but who can evidence / demonstrate a strong ability to learn and adapt to new situations are also encouraged to apply. What you'll get in return An excellent opportunity to join one of the leading pharmaceutical data and bioinformatics companies in the field, a generous salary package, a great working atmosphere, and very good career progression and development opportunities. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, as there are a number of bioinformatics, data science and statistics focused positions available. Keywords: clinical, trial, randomised, EDC, Medidata, RAVE, bioinformatics, bioinformatician, genomics, NGS, software, gene, drug, discovery, development, pharmaceutical, assay, programming, statistics, biology, computer, science, data, project, management, field, application, scientist, specialist, client, support, sales, pre-sales, training, product, technical, strategy

Machine learning bioinformatician, drug discovery. Python / R Genomics / NGS. Growing biotech Hertfordshire Your new company An exciting and innovative biotech developing the next generation of personalised cancer therapies are increasing their bioinformatics, statistics and software teams to help drive forward their drug discovery and development programs. The company is using DNA / NGS data from patients, along with their proprietary technology developed at world leading universities to produce a number of new therapies that will have a significant impact on patients and diseases such as cancer. Your new role You will be leading projects related to the discovery and development of new cutting edge personalised therapies, primarily through the analysis and interpretation of NGS data sets and biomarker identification / validation. This is a hands-on role with leadership responsibilities working as part of a cross-functional team, interacting closely with biologists, statisticians, bioinformaticians and clinical researchers. Major responsibilities will include: Utilising a variety of machine learning approaches for analysing large scale NGS datasets; Biomarker / target identification & validation; Developing & optimising machine learning tools, models, methods and approaches Project management, including setting timelines and milestones; Hands-on programming, eg in Python, R or similar; Liaising with major stakeholders; Providing mentorship and training to other members of the group; Working with molecular biologists to help interpret data and optimise experimental approaches. What you'll need to succeed As well as strong communication, organisational and time management skills, you should have: An MSc / PhD (or equivalent experience) in bioinformatics, computational biology, statistics, computer science, biology or a related subject; Hands-on experience with the analysis and interpretation of large scale NGS data sets (ideally from clinical samples); Very strong Machine Learning experience; A background in developing Machine Learning tools, methods or models; Knowledge of cancer biology, cell biology, immunology or immuno-oncology; A track record of working with genomic (eg sequencing / NGS, RNA-Seq, ChIP-Seq, methylation) or other clinical data; Strong programming/scripting skills in a language such as R, Python, Perl or similar; and Good project management skills. Candidates with knowledge / experience of biomarker discovery or validation, pharmaceutical drug discovery and/or development projects are encouraged to apply. What you'll get in return The chance to work on a range of interesting projects in a great company atmosphere, as well as the ability to directly influence the discovery and development of drugs/therapeutic products that will make a real difference to patients. You'll also be joining the company as they go into their next growth phase, so there will be chances to further develop your skills and career. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career, especially as there are a number of other bioinformatics, data science and statistics positions available. Keywords: lab, laboratory, management, system, solution, developer, bioinformatics, bioinformatician, data, science, statistics, statistical, biomarker, discovery, genetics, genomics, NGS, PCR, sequence, Bayesian, machine, learning, programmer, programming, scientist, diagnostics, molecular, python, R, C, Bash, medical, device, IVD, platform, project, manager, developer, tool, pipeline, computational, computer, oncology

Senior Insights Analyst Location: Cambridge, Cambridgeshire, United Kingdom Salary: Competitive, DOE Contract: Full Time, Permanent About the Role The Senior Insights Analyst analyses, models and transforms complex consumer and sales data into insights. There will be opportunities to grow and develop this role. About Consumer Insight & Analytics at Abcam The goal of the Consumer Insight and Analytics team is to catalyse growth across Abcam by helping the organization to transform consumer data into products and initiatives that help life scientists achieve their mission, faster. We are a team of market research, market intelligence, data analyst and data scientist specialists who enjoy working together and in our specialist areas to solve novel and knotty questions for the organisation. We are a growing team with lots of opportunities to influence the business and extend and utilize your skills across a wide range of areas. Roles & Responsibilities Agree and manage a plan for consumer behavioural and segmentation data analysis and modelling to support the organisation's decision making Data mining and statistical analysis to identify potential revenue opportunities Develop and implement measures of consumer value to identify strengths, weaknesses, opportunities and risks for the organisation and to support and challenge decision making Develop and implement models to direct and refine targeting to achieve commercial objectives Serve and deliver actionable insights to sales agents to help optimize the way they manage their business Ensure that appropriate outputs and recommendations are communicated effectively to key stakeholders across the business and enable the organisation to derive maximum benefit from this data and analysis Internal expert on the organisation's data, segmentation, analysis and modelling to ensure the most appropriate and effective methods are used Review and combine outputs and insights from different sources, conferring with colleagues, to provide joined up insight and build the bigger picture to guide business decisions About You You will be Degree educated ideally in Statistics or Mathematics and you will have held a data analytical role, delivering data management, customer insight and reporting solutions to large scale businesses. You are able to perform deep, thorough analysis of complex customer data and have experience presenting complex data to stakeholders as well as mentoring other analysts. You have some experience with SQL and advanced Excel skills and ideally some experience with Tableau and Python or R. You are an analytical thinker, methodical and inquisitive with a keen eye for details. Achieving goals and delivering results motivate you and you are adaptable and quick to learn. About us Ever since 1998, when our founder, Jonathan Milner, started selling antibodies from the back of his bike, Abcam has aimed to help scientific researchers make breakthroughs faster. We now have offices and labs in the UK, the US, China and Japan, and as we continue to grow, we remain ambitious, driven by our customers' success and their research needs. It's our goal to provide a world-standard in protein research tools, technical support and delivery. When you join Abcam, you'll join a global business with the passion and the vision to become the most influential company, and, best-loved brand in life sciences. Our culture is our key differentiator. We believe in empowering individuals, with responsibility given at an early stage. The working environment is fun and fast-paced, collaborative and outcome focused, with a strong customer focus. In addition to competitive salaries, we offer an attractive and flexible benefits package (which includes shares for eligible employees), a culture focussed on wellbeing and opportunities for growth and development. If you feel you have the necessary skills and experience to be successful in the role Senior Insights Analyst then click "APPLY" today, forwarding a recent copy of your CV for consideration in the first instance. No Agencies Please.

Bioinformatician - leading research centre, London. Data analysis, machine learning, R, Python, NGS, cancer Your new company This leading research centre, based in London, has a world-class reputation for innovative research. They have recently received significant funding to grow their team, and are looking to add several bioinformaticians to a high-performing group focusing on bioinformatics, data science and statistics supporting research on new treatments. They are recruiting people at both Bioinformatician and Senior Bioinformatician level. Your new role You'll be part of a team bringing innovative data science and bioinformatics approaches to large biological data sets to help draw insights and aid research on cutting-edge projects. You will be carrying out a mix of statistical analysis and programming responsibilities, but the primary focus will be on the analysis of NGS data to help develop new therapies and aid understanding of disease. Responsibilities will include (but aren't limited to): Analysing and interpreting sequencing / NGS data (eg RNA-Seq, DNA-Seq, WES, WGS); Developing and optimising bioinformatics software, pipelines and tools; Liaising with researchers on aspects such as experimental design and future work; Leading bioinformatics projects; Coding / scripting in languages such as R, Python, Perl, etc; Helping develop and apply novel computational & statistical methods to biological problems. What you'll need to succeed As well as excellent communication skills, and great problem solving ability, candidates must have: Strong scripting skills, ideally with Python, but other languages such as Perl or Bash are also acceptable; Experience with statistical software, eg R or Matlab; A very strong background in working with human / clinical NGS data, eg RNA-Seq, WGS, Exome or similar; Very good data analysis skills; At least an MSc (or equivalent experience) in bioinformatics, statistics, biology, computer science, statistical genetics or a similar discipline, although higher level degrees (ie PhD) are significantly preferred; Good communication skills, ideally gained from working with multi-disciplinary teams or researchers in multiple locations; A track record of working on cancer projects Candidates with experience of the following are preferred (although these are not essential): Bioinformatics tool and/or pipeline / workflow development or optimisation; Machine Learning or Deep Learning approaches, eg Random Forest, SVM, regression, clustering, knowledge of Keras, scikit-learn or similar. What you'll get in return A great opportunity to further develop your career, work on projects that will have a real effect on patients, and work on cutting-edge projects with world-class colleagues. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call me on . If this job isn't quite right for you but you are looking for a new position, please contact me for a confidential discussion on your career, as I am currently recruiting for a number of bioinformatics, statistics and data science roles. Keywords: bioinformatics, bioinformatician, data, science, statistics, statistical, NGS, WGS, WES, Exome, genetics, genomics, gene, genome, biology, drug, discovery, sequence, Bayesian, biomarker, machine, deep, learning, programmer, programming, scientist, python, R, C, Bash, platform, project, manager, developer, tool, pipeline, computational, computer, SVM, neural, net, Random, Forest, clustering

We are currently looking for a Project Chemist - Chinese Speaking to join a leading Pharmaceutical company based in the Berkshire area. As the Project Chemist you will be responsible for working with the R&D Team to develop an in depth understanding of synthetic processes relating to strategic projects. You will actively participate in the technical transfer of the synthetic processes from the UK to the agreed contract manufacturer for lab demonstration, pilot and commercial manufacture. Utilising the technical knowledge gained during the technical transfer process, assist with future process development or process improvement activities for the business. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Project Chemist - Chinese Speaking will be varied however the key duties and responsibilities are as follows: 1. As the Project Chemist you will work closely with the R&D team to develop an in depth understanding of the synthetic processes relating to strategic projects and aid in the design of the process development of chemical processes. You will attend and actively contribute to R&D meetings and ensure that all parties are updated on project milestones and deliverables. 2. You will work collaboratively with strategic project partners to enable efficient transfer of processes to plant as well as provide support during technical transfer processes to Asia. 3. As the Project Chemist you will provide support to the Commercial Team, by compiling marketing data and financial & statistical analysis on customers, competitors and market opportunities and be prepared to present findings to management. Furthermore you will ensure that Commercial Team are fully informed/supported on relevant market/business trends and ensure new product ideas are developed and evaluated effectively through conducting relevant market research activities and internal commercial and operational assessment. 4. As the Project Chemist you will ensure high standards of housekeeping are maintained and follow procedures relating to SH&E. 5. You will be required to travel to Asia during this role. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Project Chemist - Chinese Speaking we are looking to identify the following on your profile and past history: 1. Relevant Phd in Organic Chemistry or closely related discipline. You must be fluent in both spoken and written Chinese. 2. Proven industry experience in organic chemistry within a laboratory environment. 3. A working knowledge and practical experience with Synthetic Organic Chemistry and Technical Transfer and Project Management. Key Words: Synthetic Chemistry | Organic Chemistry | Chemistry | Senior Scientist | Drug Discovery | Drug Development | Synthetic | Organic | Pharmaceutical | Synthesis| Novel | Project Management | Technical Transfer | Tech Transfer 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.

Job Description Delivery of a high quality, single-site ICT service provision to St Mary's School Hampstead with a user base of circa 400 (staff and pupils). The post holder will be responsible for the development, maintenance, security and compliance of all ICT services (which includes all networked services such as the telephones, smart phones, EntrySign entry system and photocopiers). The post holder will be required to work flexibly e.g. outside or normal office hours or at weekends, to be reactive to out of hour's requirements e.g. ICT system failures or IT upgrades. The School is committed to safeguarding and promoting the welfare of children and young people and expects all staff and volunteers to share this commitment. Background Vendors and Technology currently in use: Area Vendors and technology in use Server and storage computers Dell hardware (servers and storage), VMware vSphere Desktop computers, laptops, and mobile devices Windows and Apple desktops and laptops, Chromebooks, iPads and iPhones Operating systems and applications software Windows Server, Windows 7/10, Centos/Debian, Virtualmin/Webmin, Foldr, SQL Server, IIS, Microsoft Office, various classroom applications, standard desktop applications such as Adobe Reader, PowerArchiver, etc, Logic Pro, Sibelius Patch management and security configurations GFI Languard, WSUS, ESET ESMC, Lansweeper, CyberEssentials guidelines Peripherals such as printers and interactive screens Olivetti MFCs, PaperCut, 3D printers, Promethean ActivPanels, Google Jamboard, VR devices, Clevertouch panels, music technology hardware Internet connections, firewall and threat management systems Smootwall UTM, GFI MailEssentials, Mailborder Wired and wireless networks and other network infrastructure equipment HP switches, Ruckus wireless controller and APs Email system Microsoft Exchange (2013), Exchange Online Data security and disaster recovery plan SSL certificates, Veeam Backup and Replication, LTO tape, Redstor cloud backup, Egress Switch Cloud systems and MDM Office 365, Google G Suite, Firefly, Accessit, EntrySign, VMware Airwatch, Apple VPP system Information management systems Capita SIMS, Sage Accounts 3CX telephone system Hosted with local SBC Remote access SSHD, RDS, DirectAccess Helpdesk system Lansweeper Overall Responsibility Reports to Bursar Supervisor responsibility: IT Technician Job Description The duties and responsibilities in the job description are not restrictive and you may be required to undertake other reasonable duties from time to time. Any duties should not substantially change the general character of the post. Strategic In conjunction with the Senior Leadership Team (SLT), develop a medium and long-term strategy for the development and growth of ICT in all areas of the School. Develop and implement a technical strategy and associated system architecture that meets the needs of current ICT usage and future development needs under the medium and long-term ICT strategies. Manage the ICT budget in line with management plans and ICT strategies and in consultation with the Bursar. Provide technical expertise and input to tender documentation for all current and future projects requiring services related to ICT. Demonstrate a willingness and ability to work flexibly, sometimes outside of normal core hours, in order to ensure the School's objectives are supported and that continuity of ICT services are maintained. Provide comprehensive management information and reports regarding service trends and incident analysis, using industry standard metrics. Ensure an asset register is maintained for all assets that are under the remit of the ICT department. Technical Overall responsibility for the network infrastructure and related ICT service provision to users in the School. Work as a team with the IT Technician, to provide ICT hardware and software support either by telephone, remote access or visits, this will include hardware repairs and kit disposal; routine systems, hardware and software maintenance; testing, installation and configuration of new hardware and software in a network environment. Manage ICT requirements and technical support on a day-to-day basis, dealing with a wide range of technical enquiries for PC's and peer-to-peer networks, iPads, internet connections and email systems for all staff, telephone systems and photocopiers ensuring that reliable, efficient and effective ICT services are provided to all users of the School. Remain fully aware of the best practice in respect of new and emerging ICT technologies, hardware and software and particularly the application of ICT to education and administration. Provide detailed procedural and systems documentation when required. Escalate support issues to external support service/s when necessary. Ensure that a robust disaster recovery plan is in place and regularly reviewed in light of changing circumstances. Administer and configure all switches and routers ensuring there is an up to date and accurate Network Schematic. Project and Contract Management Effectively manage agreed projects and any subsequently resulting service contracts or agreements. Manage the purchase of hardware, software, consumables and external contracts effectively with approval from the Bursar and within budget. Build effective working relationships with 3rd level service providers, suppliers of maintenance and support services where appropriate to ensure the repair or maintenance of computer systems. Ensure appropriate level maintenance contracts are in place for all equipment (e.g. ICT, telephones, photocopiers). Compliance Maintain the integrity and security of the School network at all times ensure appropriate level fire wall and system back-up solutions are in place. Ensure appropriate levels of compliance are met for Data Protection and GDPR compliance. Maintain current and develop and implement new standard ICT policies and advise upon and monitor the Staff and Pupils' Acceptable Use Policies. Ensure there is an up to date and well maintained hardware and software licencing inventory. Ensure the School complies with all Health & Safety legislation in relation to ICT use and that ICT is included in all relevant Health & Safety documents, policies and procedures. Work with the Leader of Learning of STEAM, Deputy Head and Director of Studies to ensure appropriate measures are in place to balance security and safety of pupils whilst allowing staff and pupils to utilise effectively the ICT resources. People Management Line manage and undertake staff appraisals for the IT Technician. Provide regular support and direction to the IT Technician to ensure quality of service provision and that any professional development needs are met where appropriate. Oversee the IT Technician to provide technical support for staff and pupils. Conduct individual and group training on the use of ICT resources and identify and organise the implementation of an ongoing training framework to ensure all users are able to maximise the use of ICT. Be an integrated team member, working closely and supporting the helpdesk function at all other times to ensure the delivery of completed project, fault and problem solutions to the customer base. Undertake any other duties as may be required and are commensurate with the grade of the post. The following duties are ones which all staff are required to perform: Observe health and safety procedures and work safely at all times; Be responsible for your own continuing self-development, undertaking training as appropriate to the working environment and location, and developments in your role; Promote and safeguard the welfare of children and young persons for whom you are responsible and with whom you come into contact; Undertake any other duties as required by your manager in order to meet the changing needs and demands of the School. Conduct yourself with professionalism, tact and diplomacy at all times as a representative of the School. Review This job description is provided to assist the post holder to know their principal duties. It may be amended in consultation with the post holder without change to the level of responsibility or remuneration appropriate to the post. Hours of work The normal hours of work for this position are 7:45am-4:15pm daily (1hr lunch break), although the post holder will need to be flexible to respond to the needs of the School occasionally working outside of these hours. Annual holiday entitlement 6 weeks paid holiday Pay scale St Mary's School Other Support Staff Pay Scales SS36 - SS41, currently £37,500 - £45,000. PERSON SPECIFICATION ATTRIBUTES ESSENTIAL DESIRABLE HOW IDENTIFIED Qualifications Recognised ICT Network qualification at minimum Level 4 or able to demonstrate significant experience in a similar role ITIL OR FITS Certified Microsoft Certified (MCSE or MCSA) Application Form Knowledge & Skills..... click apply for full job details

You will provide effective project management for Digital and Business Systems projects, particularly the delivery of further phases of the new RSSB website (including a Learner Management System, E Commerce, Enterprise Content Management and Marketing Solutions). Reporting into the IM&T Portfolio Manager with a dotted line to the Head of Digital, you will act as one of the key roles between the business and the project team. You will have a strong understanding of agile processes for delivering quickly and efficiently as well as understand the design and development process. You will also be comfortable communicating with the design and development teams and business stakeholders on both a business and technical level. To find out more and apply, please visit out website.

Reporting directly to the Payroll Manager - Non UK Countries, the Payroll Data Analyst will be responsible for interrogating the Jet2.com and Jet2holidays HR New Starter data, manipulating large datasets derived from the recruitment database into accurate, relevant and insightful reports in a timely manner to allow delivery of the Non-UK payrolls in partnership with the Payroll provider. Please note this position is a 20h/week fixed term contract until 31st May 2020 . You will act as first line support for all data and macro reports requirements for the payroll team. The successful candidate will be of graduate calibre with excellent analytical skills and a proven track record of analysing large and complex data sets . Attention to detail is critical, as are strong verbal and written communication skills. Advanced use of Microsoft Office, especially Excel , will be a day to day requirement for this position while an understanding of HR data processes and procedures would be highly advantageous, but not essential. 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 !!

Our client, a rapidly expanding biotech business, are currently looking to recruit an experienced Senior / Principal Scientist to help spearhead their Drug Discovery team. The work they are undertaking is truly revolutionary and as a consequence they are extremely well funded. Drug Discovery Role: Within the experienced drug discovery team, you will utilise previous experience from a medicinal chemistry / DMPK / pharmacology to add valuable experience to the team. Translate drug discovery to preclinical and clinical stages, providing effective study design input Work to provide drug discovery input to identify new developments within clinical unmet needs Compile reports that are compliant with regulatory packages Work with an exciting team of pharmacologists, bioinformaticians and software engineers Drug Discovery Scientist Profile: Excellent academic credentials from a leading university, ideally within DMPK or Medicinal Chemistry (related disciplines will also be considered) Extensive knowledge of drug discovery and development process 5+ years of experience in a commercial environment Experience with designing studies for pre-clinical purposes This is an excellent opportunity to join a company that is enjoying unrivalled growth and success within their field, and one that offers the chance to see at first-hand the impact of your work. If this role is of interest, then please contact Jamie at TEC Partners directly.

CK Group is recruiting for a Medical Manager to join a company in the Pharmaceutical industry at their site based in Walton Oaks, Surrey on a contract basis for 6 months and has a rate of £34 PAYE. The Company: Our client is one of the largest bio-pharmaceutical companies operating in the UK. They are committed to helping the UK develop the talent it needs to achieve the aspiration of being a global leader in life sciences, from the school classroom to PhDs. They are committed to working with the NHS, academia and other healthcare organisations to improve the delivery of healthcare and achieve the best health outcomes for people in the UK. The Location: The Walton Oaks site is situated a 30 minute walk from the nearest train station in Betchworth which provides regular trains to Redhill and Reading. Walton Oaks is also easily accessed by car as the site is just a few minutes off the M25. Tadworth, just 2.4 miles from site is a town in Surrey near to Ashtead, Banstead, Betchworth, Epsom and Reigate. Tadworth boasts great places to stay as well-established pubs, restaurants, attractions, activities, events and much more. The Role: This role will be responsible for Medical Plans and deliverables for the Viagra Rx/OTC Franchise for Upjohn UK. The position will require partnership and strong collaboration with the Global Medical and Commercial Organization and is the point of contact & accountability to ensure medical alignment on key strategies and deliverables. The Medical Manager provides medical guidance and input working directly with commercial, legal, safety and regulatory colleagues in support of key product initiatives. Activities may include approval of promotional activities/materials, KOL management, organizing Advisory Boards, educational meetings, managing publications, field force training as well as partnering cross functionally on product maintenance and defense activities. Primary Duties: - Responsibility for development of the Medical Plan/Strategy for Viagra Rx/Viagra Connect in UK. - Collaboration with internal stakeholders to ensure timely delivery of information on brand strategy, new clinical data, new regulatory and safety information and accurate, balanced and up to date materials to use in medical to medical communications. - Ensure compliance of all medical activities with ABPI Code of Practice, PAGB and relevant SOPs, regulations and guidelines. - Work with key external stakeholders supporting goals and bringing external insights to the organization to shape strategy and providing focused, relevant information in response to their needs. - Ensure that product materials and related activities reflect the most up to date regulatory labelling and risk management plans, regulatory commitments and meet ABPI code/PAGB/inter-company requirements. - Medical input within regulatory submissions, clinical overviews, license variations and CDS updates as required. - Input into HEOR submissions, HTA dossiers, clinical guideline consultations and regional formularies as required. - Support for investigator-initiated research (IIR) studies to ensure that appropriate records are kept, and progress is monitored. - Support media, government and patient group activities, including policy development, corporate initiatives and issues management. - Participate in local, regional and global cross-functional project teams related to the Viagra brand. - Work closely with Commercial teams to assess business development opportunities in the Urology therapeutic area. Your Background: - Medical, pharmacy or postgraduate level science degree. - Desired experience of 3-5 years in medical affairs within UK OTC environment and deep PAGB and ABPI compliance processes knowledge. - Proven ability to interact with KOLs and Government Officials. - Demonstrated ability to create and articulate medical brand strategies. - Proven ability to lead and manage in a complex environment (e.g. across markets, functions). - Knowledge of the therapeutic. 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 47027 in all correspondence.

Quality Assurance and Regulatory Affairs Manager / RP - Medical Device - West Sussex - £50,000 - £55,000 Are you experienced in Quality Assurance and Regulatory Affairs the Pharmaceutical or Medical Device markets? Are you qualified as a Responsible Person? Apply Now! The Job roles and responsibilities: As a QARA (Quality Assurance and Regulatory Affairs) Manager, your responsibilities will include: Managing Medical Affairs activities which will include supervising Pharmacovigilance consultants. Lead non - clinical product development activities. Comply fully with GDP activities and FDA regulations. Undertake the role of Responsible Person. Ensure that the Leadership team is aware of Quality or Safety issues. Ensure that regulatory filling and approvals are delivered to the timescales agreed. To be suitable for the position of QARA (Quality Assurance and Regulatory Affairs) Manager you will require the following: Registered as Responsible Person (RP) with the MHRA Experience directly with a similar role covering the maintenance, creation and submission of pharmaceutical registration documents. Life Science degree or equivalent qualification. The Package for the role of QARA (Quality Assurance and Regulatory Affairs): Salary: £50,000 - £55,000 Holiday: 25 days + bank holidays. This position is based in West Sussex and is commutable from Brighton, Crawley, Worthing, Brighton and Guilford. Please apply now to discuss your experience and the job in more detail.

Licensed Animal Technician - Dundee Looking for a new venture within Animal Technology? Look no further, here at S3 Science, we have a new opportunity for Licensed Technicians with GLP experience, to progress further within their careers. Our client is a prestigious Contract Research Organisation, with specialisms across multiple sectors. We look for problem-solvers with a proven track record in life sciences, laboratory based analytical testing and specialist consulting. The Role Working within an in in vivo laboratory environment the post holder will be responsible for performing experimental procedures to the highest level of care and welfare. The Animal Technician will assist and perform procedures for in vivo scientific studies for client and internal research in strict compliance with legislative, health & safety requirements and company SOP's/ Policies. Main Duties include: To perform experimental procedures in line with current regulatory and/or legislative requirements and to agreed company standards and productivity To be fully competent in a range of in vivo techniques with basic skills (e.g. administration via common routes & reporting clinical signs) and assist in conducting experimental studies under direction of a Chief Animal Technician and Study Directors Be proactive in gaining competency in more advanced in vivo techniques (e.g. use of anaesthetics including induction and monitoring) To be responsible for appropriate record keeping and ensuring that the results of experiments are collected promptly and recorded accurately as per SOP's and to the required standard for legislative and scientific research purposes To assist with general housekeeping of the in vivo unit such as cleaning, washing and maintenance of animal rooms Prepare study paperwork and study materials prior to study start date The position may involve other duties appropriate to the role Displaying competency in a range of in vivo techniques from basic skills to more advanced e.g. Surgical Necropsy competencies Knowledgeable about the work being undertaken and highly knowledgeable with the Home Office Animals (Scientific Procedures) Act 1986 Act as an ambassador for the business and company values, communicate effectively with colleagues throughout the business, contribute to a culture of collaboration and teamwork What do I need to apply? The application process for this role is easy, and the criteria is set below. Permitting you match said criteria, simply click and apply to the advert, and if successful, you will be contacted by a member of the team ASAP. Minimum of 5 GCSE-level education is required inclusive of science related subject. A-Levels or BTEC National Diploma in Animal Care (or related area) are preferred, as would equivalent relevant work experience in a GLP Toxicology Environment Personal Licensee Holder modules 1-3 (module 4 is desirable) Willing to relocate to Dundee or surrounding area. All successful applications are subject to S3 Science's stringent vetting and security checks. S3 Science is proud to be an equal opportunities employer and is committed to creating a diverse environment. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender identity or expression, sexual orientation, national origin, genetics, disability, age or veteran status.

On the lookout for a new role? Do you have experience in Drug Safety? Have you worked in Pharmacovigilance? Do you enjoy leading cross-functional teams? If you answered yes, then this role is perfect for you! As a Drug Safety Manager you'll lead product lead pharmacovigilance activities within the SABRR Medical function. As a Manager you are responsible for overseeing and leading the process for safety signal activities and respond to safety questions from internal and external stakeholders. This role is based in maidenhead working for a leading pharmaceutical company. Duties: * Lead the signal management process (i.e., signal tracking, leading review meetings, etc.) for assigned product(s) and evaluates safety data and signals as part of ongoing pharmacovigilance activities. Includes synthesis of data from multiple sources and authoring signal evaluation reports. * Lead signalling review process and product Safety Signalling Team meetings. Manages literature review for safety information. * Collaborates with Global Safety Officers and other SABR MDs for assigned investigational programs including clinical trial activities (protocol review, ICF review, etc.) safety committee management, data analysis, signal detection, ad hoc requests and other product activities, as assigned. * Lead processes for responding to safety questions from regulatory authorities. * Contributes to and leads initiatives for process improvement and consistency regarding aggregate reporting, clinical trial safety oversight, signal management and responding to ad hoc safety questions. * Lead and collaborates with Aggregate Reports on strategy, review and finalization of aggregate safety reports for assigned products, such as PSURs, DSURs, Pharmacovigilance Plans, Risk Evaluation and Mitigation Strategy Plans (REMS), and Risk Management Plans (RMPs). Requirements * Preferably, hold a Bachelor's Degree in biologic or natural science; or health case discipline * Minimum 7 years Pharmacovigilance experience, including experience in aggregate safety reports and safety signal management. * Strong background in clinical trial drug safety is required. * Have the ability to understand, interpret, analyse, and clearly presents scientific and medical data in verbal and written format. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

CY Partners are currently looking for a Clinical Safety Scientist to join a leading global pharmaceutical company, based at their site in Uxbridge. As a Clinical Safety Scientist, you will be responsible for the co-ordination, end to end evaluation, negotiation, and delivery of Safety Data Exchange Agreements (SDEAs) with Licensing Partners to ensure the company meet its drug safety and vigilance obligations and ensure Patient Safety. As a Clinical Safety Scientist, you will have the opportunity to lead internal projects relevant to SDEAs, change management and make significant contributions to enable or improve compliance with global regulatory requirements for drug safety and vigilance. This position is offered on an initial contract basis and is an excellent opportunity for a Clinical Safety Scientist to expand on their experience and work with a global company. For further information please feel free to contact Helen at CY Partners The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.

Global Senior Project Manager Late Phase London OR Buckinghamshire Permanent Competitive salary Clinical Professionals have partnered with a specialist consultancy who require a Global Senior Project Manager to join their team. The role will entail the running of global non-interventional and observational research studies. Responsibilities include: Planning and managing global studies to meet client specifications Provide strong leadership of cross functional teams including local country CRAs, project managers and data managers Provide strategic planning expertise, and ensure operational feasibility of clinical development plans Budget and timeline management Provide support to CRA teams with regards to protocol, therapeutic area and study procedures and SOP training Oversight of local teams to obtain ethics approvals and negotiating site contracts Candidate requirements: Life science degree or equivalent Experience in global clinical project management Experience of non-interventional and observational studies If this role is of interest please send your up to date CV to or call Nadine on .

12 Month Freelance Country Study Manager Global Pharma 2 Days Homeworking Competitive Daily Rate ASAP Start I am currently working with a Global Pharma based in Bedfordshire who are looking for an experienced contract Study Manager to join their growing teams. This role with be Respiratory and Cardiovascular focused with Country Level responsibility of local study teams. Prior experience working on Respiratory or Cardiovascular studies required at either CRA level or in a Study Management capacity. Desired experience Minimum 3 years of experience in Development Operations (CRA, Sr CRA) Excellent project management skills and experience as a project manager managing trials within UK or globally Proven ability to lead and motivate cross-functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Excellent ability to prioritize and handle multiple tasks. If you are interested in this role please reach out to me with an up to date CV at or alternatively call me on We also offer a competitive referral scheme should you know anyone who is suitable and looking.

A global Biotech and have operated for years as successful entrepreneurial business in the Biotech industry. Quality Assurance Manager, Regulatory Compliance Contract - 12 Month Contract Uxbridge Company Your company is a global Biotech and have operated for years as successful entrepreneurial business in the Biotech industry. The company is committed to delivering products to patients, known in the industry as an 'Innovative' leader that is driven by science and is commercially doing extremely well, founded over 30 years ago… if this has sparked an interest, please do read on. They develop medicines by promoting a highly collaborative culture and employees who work toward the same mission, these drugs help patients around the globe with serious diseases and illness so it vital as a team to carry on delivering while maintaining excellence. With an exceptional pipeline, you truly do not want to miss applying and working for a company like this. Please see listed responsibilities below. Job Responsibilities and skills: Lead investigator site audits, and is responsible for the preparation and reporting of such Support for and regulatory agency inspections of investigator sites. Assists in the coordination of responses to any regulatory agency findings. Participate in internal audits, may be required to lead. Fosters a commitment to quality in individuals and a culture of quality within the organization. Work is performed under limited supervision. Minimal instruction is required only occasionally. Establishes and implements new tools as necessary. Manages both routine and complex audit activities involving multiple projects and is responsible for ensuring activities are completed. Evaluates departmental and business area SOPs for fit for purpose and in compliance with regulatory requirements. Purpose is for input and obtaining information for dissemination intra- or inter-departmentally. What you need to succeed You must have Good Clinical Practise QA experience and must have conducted Investigator Site Audits. - Exceptional attention to detail - Consistently deliver high quality standards What you need to do now If you're interested in this role, please contact me via email to book in a call. If this job isn't quite right for you but you are looking for a new job, contact Leonard Joseph of Hays in London - Cheapside for a confidential discussion.

Sam Whyley-Smith at CK Clinical is recruiting for a Global Clinical Data Operations, Senior Manager to join a highly reputable global pharmaceutical company to serve as a subject matter expert and primary contact for clinical data sharing, CSR redaction and lay summary of results development. This would be a leadership position of a small team as well as being a 'hands on' position within clinical trial transparency and disclosure activities. Candidates with a background in Biometrics, Regulatory Redaction, Medical Writing and Data Management will be considered! Key Responsibilities (including but not limited to): - Identifying, tracking and managing risks by applying comprehensive knowledge of disclosure and transparency, liaising with team members and senior management, regional Compliance and Risk Management to record risks and potential mitigation and implementation strategies. - Tracking and reporting overall compliance for clinical trial transparency as per company policy for Clinical Trial Data Access and the Disclosure of Clinical Trial Information and applicable regulations. Identifying and escalating risks and issues, and proposing mitigation and remediation strategies. - Planning and managing the implementation and upgrade of specific systems projects. - Partnering with Senior Management from departments involved in transparency operations. - Partnering and leading interactions with Senior Management of departments managing studies, ensuring they and their departments are fully aware of their roles and responsibilities around transparency operations obligations, and ensure appropriate support is provided. - Working closely with vendors to ensure that the contracts are executed effectively. - Representing the company within industry working groups associated with transparency operations. - Ensuring transparency operations for upcoming and completed work is maintained and up-to-date and required documentation to show adherence to relevant SOPs is archived appropriately. - Contributing to the interpretation and assessment of the impact of emerging regulations and applicable laws to maintain compliance for their impact on daily operations and generally assessing operations processes to identify opportunities for improvements. - Preparing training materials and delivering training on end-to-end transparency operations process, important process changes, and other associated topics to all the stakeholders involved. - Leadership and line management of a small team. Your Background: To succeed in this role, you will come from a background in either Biometrics, Regulatory Redaction, Medical Writing or Data Management. You will also have the following background; - Education to B.Sc. level or equivalent. - Experience working within the clinical trial transparency and data sharing area. - Working knowledge of industry tools and solutions for preparation and sharing of data with third parties. - Experience with implementation of industry tools and solutions. - Working knowledge of preparing redacted clinical reports. - Project management experience or similar leadership type role. - Good knowledge of clinical disclosure rules such as FDAAA801, EudraCT, PhRMA/EFPIA principles for responsible data sharing, etc. - Knowledge of study registration and results disclosure on . - Excellent written and spoken English. - Managing operational processes subject to deadlines and other strict key performance indicators. - Track record of driving and successfully completing time-sensitive projects across multiple departments. 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 47048 in all correspondence.

Senior Clinical Research Associate (SCRA) job, CRO, Oncology, Phases I-IV Senior Clinical Research Associate (SCRA) Your new company This world renowned and globally based CRO company are looking for the right dynamic and organized person to fit in as a Senior Clinical Research Associate as part of their Clinical Operations team. This is a unique opportunity to work for a CRO that provides services for biotechnology, pharmaceutical, medical device and government and public health industries and help realise their vision of becoming the number one partner in drug development. Their goal of reducing the time and cost of development whilst simultaneously increasing quality, requires only the best and brightest - putting you in good company. Your new role Your will be working in a large scale, fast paced environment, working alongside a team of CRA's in order to identify, select, initiate, monitor and close-out investigational sites for clinical studies (Phases I-IV). A bachelor's degree in science or equivalent is essential and you must have 2-3 years experience as a CRA on clinical studies (in a CRO or Pharmaceutical company). Furthermore, the role will require previous proven experience in Oncology. What you'll need to succeed Main Responsibilities Identify, select, initiate, monitor and close-out investigational sites for clinical studies (Phases I-IV) Ensure adherence to SOPs, regulations and ICH-GCP Assist in the training and mentoring of CRA I & CRA II's What you'll get in return This is a unique opportunity to work for a CRO that is responsible for the global development of drugs and devices that save lives and improve the quality of life of millions. This role has many internal growth opportunities and is ideal for those looking to move to management in the near future. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPPLYING TO THIS CAREER OPPORTUNITY JOB VACANCY - SENIOR HYDROLOGIST Due to increasing workloads and future development plans we have an exciting opportunity for a pragmatic, experienced Senior Hydrologist, to join our friendly team in a relaxed but professional environment. Hafrenwater is a small, dynamic consultancy, based in Shrewsbury, involved with a wide range of water-related projects throughout the UK. We provide services to the minerals, waste, housing and environmental sectors, amongst others, and have many established clients and a varied and growing remit. We are looking for an experienced Senior Hydrologist who is self-motivated and able to work with a minimum of supervision. The successful candidate will be practical and able to produce both quantitative and qualitative flood risk assessments, as well as other hydrological assessments, to a very high standard. Ideally experienced with client liaison and a background that includes knowledge of regulators throughout the UK, including Lead Local Flood Authorities. The right candidate will have the opportunity to develop their role and the future direction of the hydrological function of the company. The role will involve site visits throughout the UK, occasionally requiring overnight stays. Good reporting and computer skills are essential and more specialised ability with rainfall-runoff and hydraulic flood routing models is also highly desirable. Specific requirements are as below; • A relevant degree and postgraduate qualification in hydrology or a closely allied discipline • 5 - 10 years-experience, including employment within a consultancy environment • Good working knowledge of EA, NRW, SEPA and LLFA requirements • Experience of rainfall runoff methodologies (eg FEH, ReFH2) GIS (QGIS) • Excellent report writing, oral communication and organisational skills • Demonstrable experience of working on projects delivered to tight deadlines and within set budgets • Ideally experience in preparing or assessing industry standard 1D, 1D/2D linked and 2D modelling software such as ISIS/Flood Modeller Pro TUFLOW and HEC-RAS • Ideally some experience of Micro Drainage Excellent opportunities exist for career progression for the right candidate. It is intended that potential will exist to shape the future development of the hydrological function of Hafren Water. Terms and conditions are commensurate with the ethos of small consultancy and include pension contributions, profit related bonus and flexibility of working. Applicants interested in this opportunity should send a letter stating their suitability for the position and what they can contribute to Hafrenwater, and a CV, including two references, to debbie.sudlow(at)hafrenwater.com. The covering letter must also include details of current salary and salary expectations.

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPPLYING TO THIS CAREER OPPORTUNITY JOB VACANCY - SENIOR HYDROGEOLOGIST Due to increasing workloads and future development plans we have an exciting opportunity for an experienced Senior Hydrogeologist, to join our friendly team working in a relaxed but professional environment. We are looking for an experienced, enthusiastic, Hydrogeologist who is able to work with a minimum of supervision. The successful candidate will manage project inputs related to environmental and water resource studies and be able to produce both quantitative and qualitative work to a high standard. Ideally experienced with client liaison and negotiation with regulators throughout the UK, the candidate will need to have proven capabilities with project and financial management. In exchange, the right candidate will have the opportunity to develop their role and the future direction of the hydrogeological function of the Company. This is a permanent, full-time role and will include site visits throughout the UK and occasional overnight stays. Responsibilities: - Preparation of costed project proposals and project management from cradle to grave - Liaison with regulators and clients and establishing client relationships - Preparation of Hydrogeological Impact Assessments for Planning Applications for a range of developments including mineral extraction sites and landfills - Planning and implementation of field investigation groundwater programmes - Interpretation of analytical and monitoring data - Preparation of interpretive reports and hydrogeological risk assessments in support of Environmental Permit applications (groundwater discharges, Landfill permits, Permits for Recovery of waste materials etc) - Detailed quantitative controlled waters risk assessment and risk assessment modelling (desirable) Experience and Qualifications Required: - Degree in Geology or related Earth Science with an MSc in Hydrogeology - Minimum of 5 years post qualification experience, much of which will have been gained within an environmental consultancy - Membership of a professional body and relevant Chartership (or working towards this) preferable - Ability to work well in teams, work well under pressure and meet deadlines - Excellent planning and organisation skills - Strong technical report writing skills - Strong commercial awareness - Full clean driving licence The Package Includes: - A competitive salary - NEST pension scheme - Profit related bonus scheme - Working closely with senior Management/Directors - Working on a wide variety of projects - Opportunity to progress your career and influence the hydrogeological direction of the Company - CPD support and mentoring Applicants interested in this opportunity should send a letter stating their suitability for the position and what they can contribute to Hafrenwater, and a CV, including two references, to debbie.sudlow(at)hafrenwater.com. The covering letter must also include details of current salary and salary expectations.

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPPLYING TO THIS CAREER OPPORTUNITY Do you want to make a long-term difference to the people and places of Wales? Are you passionate about protecting the nation against flooding threats and helping the nation adapt to the impacts of climate change? We are looking for enthusiastic, driven and adaptable individuals to join our Flood Risk Analysis Team. Team players, people with bags of energy and a real passion for the environment - apply now! Following a recent re-organisation, we have several exciting opportunities to join our Flood Risk Analysis Team in North Wales. As part of an established and well-respected team you will use flood modelling and collection and analysis of post flood event data to develop the evidence that helps to identify communities at risk of flooding and help to prioritise flood risk management actions to higher risk communities. Flood Risk Analysis Advisor 1 - Full time, permanent role, £25,828 rising to £29,352 over four years (subject to performance). The post holder will work as a key member of the Flood Risk Analysis team in providing and producing timely and accurate flood risk information that underpins NRWs flood risk work. They will be involved in preparing complex flood map information using GIS, speaking to external customers, management of existing data & information, carrying out post flood investigations and reporting. A good understanding of flood risk issues is essential along with a basic understanding of flood estimation and modelling software. As part of the role and building on existing experience the post holder will undertake simple hydraulic modelling work on smaller scale projects This post can be based anywhere in North Wales - Our offices are in Bangor, Buckley, Dolgellau, Llanrwst, Ruthin and Welshpool As part of #TeamNRW you will also be eligible for the following benefits; • A competitive salary • A generous career-average Civil Service pension • 28 days annual leave, rising to 33 days over 5 years • Flexible working options • Occupational health including advisory services and eye care • Tax free childcare • Salary sacrifice schemes. Closing date: 16 December 2019 Interviews: Early January 2020

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPPLYING TO THIS CAREER OPPORTUNITY Do you want to make a long-term difference to the people and places of Wales? Are you passionate about protecting the nation against flooding threats and helping the nation adapt to the impacts of climate change? We are looking for enthusiastic, driven and adaptable individuals to join our Flood Risk Analysis Team. Team players, people with bags of energy and a real passion for the environment - apply now! Following a recent re-organisation, we have several exciting opportunities to join our Flood Risk Analysis Team in North Wales. As part of an established and well-respected team you will use flood modelling and collection and analysis of post flood event data to develop the evidence that helps to identify communities at risk of flooding and help to prioritise flood risk management actions to higher risk communities. Flood Risk Analysis Advisor 2 - Full time, permanent role, £30,120 rising to £33,383 over four years (subject to performance). The post holder will produce, manage and deliver flood risk information and evidence that underpins the work of NRWs Flood Risk Management and Operations teams. They will primarily be responsible for building and checking 1D/2D hydraulic models of rivers, project management of Consultants, report writing and data management. They will be working in a team of similar experienced technical staff, delivering a risk-based service across North & Mid Wales and involved in NRWs emergency Response to flooding as a CAT 1 Responder. This post can be based anywhere in North Wales - Our offices are in Bangor, Buckley, Dolgellau, Llanrwst, Ruthin and Welshpool As part of #TeamNRW you will also be eligible for the following benefits; • A competitive salary • A generous career-average Civil Service pension • 28 days annual leave, rising to 33 days over 5 years • Flexible working options • Occupational health including advisory services and eye care • Tax free childcare • Salary sacrifice schemes. Closing date: 16 December 2019 Interviews: Early January 2020

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPPLYING TO THIS CAREER OPPORTUNITY Do you want to make a long-term difference to the people and places of Wales? Are you passionate about protecting the nation against flooding threats and helping the nation adapt to the impacts of climate change? We are looking for enthusiastic, driven and adaptable individuals to join our Flood Risk Analysis Team. Team players, people with bags of energy and a real passion for the environment - apply now! Following a recent re-organisation, we have several exciting opportunities to join our Flood Risk Analysis Team in North Wales. As part of an established and well-respected team you will use flood modelling and collection and analysis of post flood event data to develop the evidence that helps to identify communities at risk of flooding and help to prioritise flood risk management actions to higher risk communities. Flood Risk Analysis Senior Advisor - Full time, permanent role, £34,427 rising to £37,656 over four years (subject to performance). The post holder will bring significant experience within FRM and will provide professional / technical leadership across the programme of flood risk modelling work undertaken by the FRA Team and wider within NRW. They will lead and influence work with our professional partners, senior managers and Welsh Government and actively contribute to specialist FRM Sub groups in developing Policy and Guidance. They will have excellent project and budget management experience with experience of delivering large complex projects and excellent knowledge of hydraulic modelling and hydrological analysis (expert practical knowledge of 1D/2D fluvial or coastal modelling software).They will be working in a team of similar experienced technical staff, delivering a risk based service across North & Mid Wales and involved in NRWs emergency Response to flooding as a CAT 1 Responder, including representing NRW in Tactical Command during flood incidents. This post can be based anywhere in North Wales - Our offices are in Bangor, Buckley, Dolgellau, Llanrwst, Ruthin and Welshpool As part of #TeamNRW you will also be eligible for the following benefits; • A competitive salary • A generous career-average Civil Service pension • 28 days annual leave, rising to 33 days over 5 years • Flexible working options • Occupational health including advisory services and eye care • Tax free childcare • Salary sacrifice schemes. Closing date: 16 December 2019 Interviews: Early January 2020