1372 Science jobs

Exciting opportunity for an accomplished Laboratory professional to join a successful contract testing organisation on an initial 6-month contract. Key responsibilities include: Performing testing for the packaging industry, working with specialist equipment Recording data and writing detailed reports to GDP standards Communicating with clients and suppliers, including hosting site visits Sample handling and equipment maintenance The successful candidate must have: A minimum of 6 months experience within a GDP regulated laboratory Excellent report writing and literacy skills Excellent communication skills and the ability to work well within a team environment This role is offered on an initial 6-month FTC with scope to become permanent. Apply now to be considered! Key words: Laboratory, packaging, testing, GDP, good documentation practice, vibration, climatic, compression, Surrey, VRS6548AW Follow VRS Recruitment on LinkedIn to view all our latest vacancies! 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.

REED Scientific are currently working with a growing Multinational Pharmaceutical manufacturer company in the North West area. The company is looking to recruit a Quality Auditor to join their team. This role is commutable from Manchester, Stockport, Macclesfield and other locations based in North West. You will be involved in: - Auditing site operations and procedures -Writing and updating SOPs -Conduct work to GLP and GMP standards - Carrying out internal audits to support the Quality management system Are you right for the job? You will have: - Chemistry degree or similar subject -Previous experience of working as a Quality Auditor - Knowledge of QMS including CAPA, NCRs, OOS/OOT - Knowledge of conducting work to GLP and GMP standards Please apply today to avoid missing out on this great opportunity as the company is looking to carry out interviews in the next 2 weeks.

Lab Technician (6 month contract) £9.46 an hour The Company Perfect opportunity for a recent science graduate! My client is a major global healthcare company. They now have an exciting opportunity at their site in Loughborough for a recent science graduate to join their team. The Opportunity This opportunity is suitable for someone who is wanting to go into the scientific industry. Duties include: Performing analytical testing Completing LIR investigations Routine testing for incoming samples UV/IR analysis Plus much more! About you: Recent Science graduate GMP knowledge Good attention to detail My client has a number of positions available at the minute ranging from Lab Technicians to AR&D Analysts. Apply now! For more information, feel free to contact Jak at Consult Search or message/connect with Jak on LinkedIn.

Hyper Recruitment Solutions are currently looking for a Medicinal Chemist to join a leading Bio- pharmaceutical company based in the Hertfordshire area. As the Medicinal Chemist you will be responsible for the drug design and synthesis of new drug candidates. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Medicinal Chemist will be varied however the key duties and responsibilities are as follows: 1. You will play a pivotal part of developing new synthetic methods as well as synthesising key intermediates and small drug candidates. 2. As the Medicinal Chemist you will carry out the purification and characterisation of compounds, contributing to the research team by synthesising key intermediates and small molecule drug candidates as well as developing new synthetic methods when required. 3. As the Medicinal Chemist you will support the preparation of IP documents, whilst maintaining high synthetic chemistry productivity. 4. You will be responsible for the maintenance of laboratory experiments in accordance with company policy. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Medicinal Chemist we are looking to identify the following on your profile and past history: 1. Relevant degree in a Synthetic Organic Chemistry or Medicinal Chemistry related degree. 2. Proven industry experience in practical synthetic chemistry, you will demonstrate excellence in theoretical and practical synthetic chemistry, having an excellent knowledge of medicinal chemistry design principles, including structure-based drug design and the influence of physiochemical properties. 3. A working knowledge and practical experience with medicinal chemistry design principles, including structure-based drug design and physiochemical properties. Key Words: Medicinal / Chemist / Synthetic / Organic / Drug Design / Drug Discovery / Drug Synthesis 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.

CK Group is recruiting for a Microbiologist to join a company in the healthcare industry at their site based in Ulverston on a contract basis for 6 months and has a hourly rate of £11.54 PAYE. The Company: Our client is a world leading research-based pharmaceutical company that combines both individual talent and technical resources to create a platform for the delivery of strong growth in a rapidly changing healthcare market. Their mission is to improve the quality of human life by enabling people to do more, feel better and live longer. The Location: This role is located in Ulverston and is approximately a 10-15 minute walk from the train station. Ulverston is a fine market town in the centre of the Furness peninsula, with old buildings and a labyrinth of cobbled streets, and is the start of the 70 mile Cumbrian Way. Role Purpose: To assist in providing a microbiology testing and monitoring support service to the site functional areas (primarily product stream) that ensures product manufactured at Ulverston is of appropriate microbiological standard, complies with specifications, customer and the various regulatory authority requirements. Key Responsibilities: - As part of a team, carry out microbial analysis of the process and materials associated with pharmaceutical manufacturing. - Carry out microbial analysis of raw materials, components, intermediates and final products as well as environmental monitoring of the site. - Be responsible for the maintenance, culture, speciation and enumeration of microorganisms, and support the regulatory area, QA audits and inspections (MCA/FDA). Your Background: - Ideally a graduate in microbiology, with experience in isolation and speciation techniques. - Must have good aseptic techniques. - GLP knowledge and an understanding of pathogenicity and ecology of microorganisms would be useful. - Experience in physical monitoring of areas. - Experience working to GMP. 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 47197 in all correspondence.

Our client has an exciting opportunity for a Data Technician (Hydrologist) to join their growing team in their Exeter office. Salary £16500 - £30000 Depending on experience Part Time and Full Time positions available The role The role involves processing and reporting of water quantity (flow), depth, quality and rainfall data etc, collected by their field teams. It will also include some fieldwork, which will comprise visiting various sites throughout the South of England to undertake field measurements of water quantity (flow), depth, quality, rainfall etc, plus the operation and maintenance of telemetry logging equipment. This is a flexible role with field days dependent on daylight hours and although normally Monday - Friday, these may be flexible too. The person GCSE or equivalent in Geography, Maths and English Good level of computer literacy (MS Office - Word, Excel etc) Full UK driving licence Hands on practical skills Comfortable working in water, able to swim Desirable Installation skills, including the use of Power and Hand tools. A Level or equivalent in Geography Degree or other suitable qualification in a related environmental discipline (e.g. Env. Science, Geography , Outdoor Education etc)

Process Research & Development is seeking a highly motivated and experienced technical writer to join our Manufacturing Development group at Oxford BioMedica. Key responsibilities and accountabilities: Author clear and concise documentation including protocols and scientific reports to support Upstream and Downstream process development activities in order to contribute to the overall group objectives in line with company objectives Review documentation including protocols and technical reports within Process R&D group, ensuring project objectives are met within a set time frame Possess a sufficient level of knowledge to interpret experimental results. Analyse and interpret data, and present/document the results at meetings. Generate reports and prepare scientific presentations as needed Maintain a high standard of record keeping and documentation so that information is clearly captured, disseminated and reported. Disseminate critical findings which may have a business impact to other departments within the company. Possess good knowledge of project area literature and upcoming technologies and ensure up to date with current thinking and literature. Compile reports of scientific data and project findings with clear conclusions and recommendations for internal and external review. Contribute to the scientific and business needs of the company. Maintain a high ethical standard and a commitment to producing high quality work. Report results of the group to head of department and senior management. Present data at internal and external meetings and conferences to peers and subject leaders in the field. Prepare manuscripts for publication and documents for patent applications, regulatory authorities and external collaborators. Responsible for ensuring all scientific or proprietary data is submitted to PatentSafe or recorded in appropriate official documentation. Key skills and requirements: A graduate or postgraduate degree (or equivalent level qualification) in a relevant science Relevant, practical industry experience in authoring cell culture/upstream/downstream reports A sound understanding of basic biopharmaceutical process development activities Excellent written and verbal communication skills Experience of managing multiple projects Excellent organisational and time management skills Ability to prioritise workloads and work under pressure Good attention to detail Highly motivated Person Specification: Industry experience in authoring cell culture/upstream/downstream projects/activities with substantial relevant experience A good knowledge and experience of developing biopharmaceutical based technologies A highly motivated, enthusiastic, positive attitude About Process Research & Development The Process R&D group has a core function within Manufacturing Development. It consists of experienced scientists and engineers that have extensive expertise in all aspects of upstream and downstream development. PR&D take processes from the laboratory "bench" scale and apply process expertise and engineering fundamentals for systematic evaluation, optimisation and understanding for delivery to Manufacturing. As the focus shifts towards delivering processes and materials to support our LentiVector® platform products through later-stage development and market supply, PR&D is well positioned to ensure our products are manufactured using processes that are scalable, robust and reproducible as well as commercially viable and regulatory compliant.

A growing company is looking for a Technical Pharmaceutical Trainer to join our Technical Manufacturing Training department. This is a permanent position based at our Slough facility. As a Technical Trainer you will be part of a team; providing training on cGMP (current Good Manufacturing Practice) procedures to incumbent staff and new hires to enable them to become effective contributors to the Manufacturing Plant. Client Details They come to the company for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Description Onboarding new hires ensuring they are suitably trained and compliant in the use of equiptment and learning modules to include SOP's (standard operating procedures) Conduct practical technical training sessions and assessments within a manufacturing environment with due regard to cGMP requirements Carry out regular technical assessments to qualify staff in critical cGMP procedures Co-ordinate the execution of training programs in consultation with the area manager Ensure staff training documentation is completed in compliance with cGMP Execute and further develop new starter technical training program in consultation with the area managers Monitor the effectiveness of training Identify improvements to the training program and implement continuous improvement activities Promote understanding by providing staff with background knowledge of the methods used in manufacturing Conduct technical training on mammalian cell culture including the use of bioreactors, chromatography steps, filtration and aseptic procedures Profile Experience of training in a Manufacturing or regulated environment Ideally Practical Manufacturing experience within a cGMP environment Excellent coaching and communication skills Job Offer Health insurance Pension Dental Insurance 26 days holiday plus bank holidays

Job Title: UK Laboratory Manager Job Type: Permanent Hours: 37.5 per week Job Location: Milton Keynes Salary: Competitive As the UK Laboratory Manager, you will be responsible for the operational delivery of the SGS IBR Laboratory, and will oversee the delivery of filtration and consumer product analytical services to customers. Day to day you'll be responsible for the delivery of budgeted laboratory revenues and profits through active teamwork with other Managers on site, ensuring efficient and appropriate use of resources/facilities and the operational capability to deliver a valued overall service to IBR customers through teamwork with other IBR managers globally. You will lead the laboratory team in the effective employment of motivated and competent people who are consistently able to deliver high quality and valued laboratory services to the standards required by customers and ISO 17025 Accreditation. As the UK Laboratory Manager, you'll receive a competitive salary, you'll also benefit from a performance bonus, retail discount scheme, private health cover, a contributory pension scheme and life cover. YOUR PROFILE To be successful in the role you'll need extensive experience in a laboratory management role related to the filtration industry. You'll have experience of directly communicating with clients and successfully resolving client issues/complaints and will have experience of managing a successful team, including performance management, recruitment, managing underperformance. You'll need to show a thorough understanding and knowledge of H&S procedures to OHSAS 18001 standard such as risk assessments, and will have the ability to identify and capitalise on business development/efficiency opportunities to ensure sustainable revenues at acceptable margins. In addition to the above you'll also need to demonstrate the following; In-depth technical knowledge of analytical testing activities within the filtration and vacuum cleaner industry, in particular ISO 29463, IEC 62885-2, ASTM F1977, etc. Good communication skills - both verbal and written. Good organisational skills Experience in fluid dynamics, vacuum cleaner and filter testing a positive Able to adopt a flexible approach to work and react effectively to a rapidly changing environment within a fast paced laboratory with short customer turnaround times. Working knowledge of effective people management techniques, e.g. coaching, appraisals, objective setting, etc. Able to work under own initiative and with a high degree of autonomy & maturity. Qualifications: Educated to degree level in Engineering discipline (or equivalent) ABOUT SGS SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential. At SGS, we have an open corporate and international culture, we offer a dynamic work environment in a leading global company. Our high professional standards and our sustainability approach guarantee you a future-oriented work environment. We invest in our employees for the long term and we are committed to supporting your development within the company. APPLY NOW for full consideration, you can be sure that your application will be treated confidentially and impartially, and you will always receive an update within 10 business days.

Role: Laboratory Technician Location: Liverpool Type: Permanent Salary: Entry Level Our client is a global medical device / microbiology company, looking for a newly experienced Laboratory Technician for the QC department. Role: Adhering to SOPs & regulatory standards at all times Writing & preparing reports & implementing amendments Testing raw materials/finished goods, & product end of shelf-life Performing calibrations/verifications of instruments where required Performing water testing/environmental monitoring Investigating complaints & product rejections where required Maintaining a safe & clean laboratory environment Ensuring correct disposal of waste Candidate Requirements: BSc or equivalent in a Life Science related discipline (with an element in Microbiology- gram staining, sterility, culture media etc ) 12 months laboratory experience in an ISO9001 / 13485 / 17025 environment (essential) Excellent planning & organisational skills Excellent written & verbal communication skills Computer literate Driven & motivated to learn new skills Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h u s s e l l - t a y l o r . c o . u k

Looking for GCSE / A-Level Science qualified individuals interested in a career working for a pioneering scientific company Oxford BioMedica is a pioneer of gene and cell therapy and our work is helping to deliver life changing treatments. Gene and cell therapy is the treatment of disease by the delivery of therapeutic DNA into a patient's cells, providing long term and potentially curative treatments for a wide range of diseases. With the potential to transform medicine, the sector holds significant promise with the first commercial products now launched and others rapidly approaching the market. Our recent successes are driving significant growth. As such, we are looking to recruit a Laboratory Technician to join our Analytical Services Group. The purpose of this role is to provide essential laboratory activities and services to support analytical testing within the category 3 laboratories to ensure timelines are met and that the laboratories are maintained to a high standard. . Key responsibilities and accountabilities: To maintain cell lines used by ASG and other OXB departments To perform routine monitoring of controlled temperature units within our laboratories To liaise and work with Laboratory Management to organize equipment servicing and equipment repair To liaise and work with Laboratory Management to organize specific activities, for example fumigation To perform regular stock checks of consumables and reagents for our laboratories and order as required To clean laboratory equipment and facilities To operate the autoclave and dispose of waste materials Provide support to laboratory technicians & scientists when performing analytical assays. Key skills and requirements: A Level or equivalent experience in a scientific subject Experience working in a GMP laboratory & facilities would be advantageous, but not essential Person Specification: Attention to detail Able to follow instructions 'Can do' attitude Due to the career path for these roles, they are better suited to non-graduates. No agencies please

An opportunity has arisen for a process chemist to join a specialist chemical manufacturing organisation in the Kidderminster. As a process chemist, you will be responsible for a range of manufacturing processes and development methods in order to optimise the operation of pilot plant and production scale. To be successful you should hold a relevant scientific qualification and possess commercial experience within a chemical process/manufacturing environment. Process Chemist Responsibilities: Assume control of the chemical manufacturing processes. Liaison with other manufacturing/test areas, especially in the manufacture of hazardous and sensitive materials. Operation of plants on a pilot plant scale or production scale. Process monitoring and analysis. Computer control of safety-critical manufacturing processes. Inventory management and test clearance of materials Health, Safety and Environmental monitoring routines. Skills and Requirements: As a minimum requirement you should be educated to degree level in chemistry or closely related discipline. Possess commercial experience within a chemical process/manufacturing environment. A strong foundation in analytical chemistry techniques would be advantageous. Working knowledge of chemical safety and environmental impact is essential. Possess a methodical approach to your work with excellent problem-solving skills. Excellent communication skills with the ability to work under pressure to meet deadlines. Salary - £30,000 - £40,000 + Benefits - Pension Contribution - Free Parking - Subsidised Canteen - 25 Days Holiday Working Hours: 37 hour week: Monday- Thursday 7:30 -15:30 + Friday 07:30 -14:30 If you are looking for a new exciting challenge with a specialist chemical manufacturing organisation then please send your CV to or get in touch:

Job Title: Industrialisation Engineer (Medical Devices) Salary & Benefits: £40,000 & private healthcare (BUPA), 24 days holiday, matched pension Location: Cambridge This is an excellent opportunity for an up and coming Industrialisation Engineer to join a successful medical engineering business that specialises in the development of innovative novel drug delivery systems. Your primary area of responsibility will be support the development team during both concept and detailed design phases to ensure the commercial suitability for manufacture. The Industrialisation Engineer will need to have experience working in a similar role with knowledge of injection moulding of polymers for complex precision products. You will also need to have experience selecting and procuring capital equipment for pilot-scale manufacture, and developing manufacturing processes and techniques. Industrialisation Engineer Requirements: Degree trained within a relevant technical/scientific area Experienced in injection moulding of complex multi-cavity products Knowledge of tooling design and DFM Some experience in the procurement of capital process equipment and tooling Knowledge of regulatory requirements (ISO13485, ISO14971, cGMP and CFR2010/211) Excellent communication and interpersonal skills If you are interested in this Industrialisation Engineer opportunity, click Apply Now and we will be in touch with you soon.

Naynesh at CK Science is recruiting for an Antibody Scientist/Production Scientist to join a growing Biopharmaceutical company at their site near Hitchin (Hertfordshire) on a permanent basis. This role is offered with a competitive salary with excellent benefits (flexible working, share options, pension, private healthcare, bonus structure and subsidised restaurant, shop and more). My client is expanding their team and looking for a Antibody/Production Scientist to work within their discovery team to discover and develop new antibodies. The Company: Our client is developing a unique and innovative class of Antibody Drug Conjugate (ADC) therapy, and has developed their technology platform and developing their first oncology products in areas of high clinical unmet need. This company has an advanced and focussed approach which will create a major opportunity to bring differentiating products for solid cancers into clinical development. Location: This role is located in Stevenage, easily commutable from both Cambridge and London. Responsibilities: - Maintain a high level of knowledge and skills in technical R&D areas related to Antibodies and Antibody-drug conjugates (ADCs). - Communicate technical knowledge both internally and externally, with staff and collaborators at internal meetings, presentations and conferences. - Carry out laboratory R&D using Good Laboratory Practice (GLP). Your Background: - BSc/MSci degree in Biology, Biochemistry or related discipline. - Relevant PhD in a protein or antibody engineering-related subject. - Post-doctoral experience would be advantageous. If no PhD, then my client would be looking for someone with commercial experience in a biotechnology/industrial environment. The successful candidate must possess the relevant skills to be considered for this role: - Experience in display techniques (phage, ribosome, yeast) such as library construction and performing selections. - Molecular biology techniques to design and construct genetic constructs for the production of antibody, antibody-derived or other proteins of biotechnological interest to express in different host organisms (bacteria, yeast and mammalian cells). - Large (lab) scale production of recombinant proteins and purification to a high degree of purity using affinity chromatography, ion exchange and size exclusion techniques (AKTA, systems and supporting UNICORN Software). - Develop, validate and use analytical methods to study antibodies, such as SDS-PAGE, Immunoassays, Chromatography, BIAcore/SPR. The Benefits: - Competitive salary/flexible working/share options/pension scheme/private healthcare/access to subsidised restaurant, shop, sports centre, and shuttle bus to and from Stevenage station. 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 47203 in all correspondence.

Production Engineer - Medical Devices - Liverpool Either 3 Month Contract (c£17 per hour) Permanent position (c£35-£40k) Key area's Please apply if you are a Production Engineer or Manufacturing Engineer with; A Medical Device Background Experience in Process Efficiency & Lean 6 sigma projects for Medical Device Manufacturing Ideally have a Mechanically bias background Please apply now to be considered Production Engineer overview As part of the engineering team, your project management and stakeholder engagement skills will shine, being responsible for the project management of production aspects for the introduction of product/processes. In collaboration with the production and quality departments, you will coordinate projects to identify anomalies, bottlenecks, and product and process deviations within the manufacturing environment, implementing solutions resulting in improvements to production efficiency and minimisation of errors. As the process expert within the manufacturing environment, you will support the production department in providing the necessary information and training and by transferring technical knowledge regarding the production processes. You will ensure correct and timely preventive maintenance and calibration is performed on all production equipment and coordinate the control of change for new tools or equipment introduced into production. In addition, you will support Kaizen and 5S projects as part of the implementation of lean manufacturing principles. Requirements for suitable applicants (All should be Production Engineering within Medical Device/ISO13485 as a mininum) You have an undergraduate degree in an engineering or scientific discipline with at least 3 years of work experience in a similar function within a production environment. You are passionate about continuous improvement and have the analytical skills and working knowledge necessary for problem solving and process improvement. Your excellent communication, project management and organisational skills enable you to report and implement these improvements and sets you on the path to success. Desirables Experience of medical device manufacturing within an ISO 13485 environment Experience of process optimisation / process value stream mapping Experience of validating equipment, processes and test methods 6-sigma / lean principles qualifications Please apply now to be considered immediately

A Cleanroom Assembly Technician is required by an expanding medical device manufacturing company in Didcot, Oxfordshire. This is an excellent opportunity to join a growing business and contribute to their ongoing success. The role requires excellent attention to detail and a background in manufacturing and/or assembly. As Cleanroom Assembly Technician duties include: Assembly of a range of medical products in a cleanroom environment Controlling goods-in, making sure paperwork is checked and completed correctly Picking and packing orders ready for dispatch Ensuring compliance with quality standards and ISOs Key Skills and Requirements as Cleanroom Assemblt Technician: Excellent attention to detail Relevant experience in a similar manufacturing / production environment Cleanroom or medical device experience would be a distinct advantage This is a great opportunity to join a friendly company at an exciting time, the ideal candidate will be motivated to contribute to the growth of the business and be looking to progress through the organisation in the future. Keywords: Medical Device Technician, Assembly Technician, Medical Device Technician, Cleanroom Assembly Technician, Quality Control Technician Bond Williams Professional Recruitment are an equal opportunity employer and operate as an Employment Business and Recruitment Agency

QC Scientist (Live-Bio department) Deeside Salary To £23,000 - depending on experience The Company We are working with a fast-growing contract pharmaceutical development company. They employ over 100 people with customers all over the world. They are an entrepreneurial business by nature and encourage their employees to shape and become the future of their company. They are seeking a QC Scientist to join their growing Live-Bio department - generally working with live-bacteria pharmaceuticals, such as a tablet, that will be containing an amount of biotherapeutic microbes. The Role What you'll do as the QC Scientist: In summary main duties will be: Performing Stability/IPC/Final Product Release testing across a range of tests following training. Potential development work around Live Bio products. Ensuring accurate reporting of results in BAR's, including checking analytical data to GMP. Reporting OOS and OOT and investigating following training. Deviations and CAPA. Liaising with QA for timely close out of work. Mentoring and training. Work with a Right First Time ethos. Adhere to all H&S policies and procedures. Observe and comply with Good Manufacturing Practice (GMP) and adhere to company policies and procedures as per the Quality Management System (QMS) and the employee handbook Conduct all work in, and maintain, the laboratory in a clean, safe and compliant condition Production of Risk and COSHH assessments. Your background: You'll have experience of working within a laboratory setting with excellent attention to detail and good documentation skills. You'll be able to prioritise your own workload with an innovative "can do" attitude that is quality focused. On this occasion, LiCa Scientific is acting as an employment agency.

Mechanical Engineer Location: Cambridge Job description The Mechanical Engineer will join my client in the instrumentation department, interfacing with a rapidly growing team that combines experts in chemistry, biochemistry, surface science and engineering to develop a new device to revolutionise and democratise the field of DNA synthesis. The role represents a great opportunity to help shape this emerging R+D team and to be involved in the exciting field of biotechnology research. Specific responsibilities include but are not limited to: providing robust and novel fluidic and mechanical engineering designs to address the issues facing the design team. fabricating, iterating and implementing those designs by embracing sound experimental-science methods hands-on in the laboratory. sourcing COTS parts wherever necessary to streamline the design process. managing the automation and interfacing of sub-components and whole instruments created both in-house and with partners. interacting effectively with other team members to understand and solve the biological problems that arise. Required qualifications Mechanical Engineering degree or equivalent A minimum of 2 years' design experience with demonstrable results First-hand knowledge of automation and control systems Familiarity with liquid-handling including fluid mechanics and/or microfluidics theory and practice Demonstrated ability to perform experiments and produce practical results in a laboratory or workshop environment Desirable qualifications and skills A PhD in a biotechnology-relevant engineering field Programming background, e.g., in C/C++, MATLAB, LabVIEW, especially on microcontrollers, Arduino, Raspberry Pi, etc. COMSOL or other finite-element based modelling / simulation experience Some practical knowledge of biology (understanding DNA, RNA, e.g.) with the ability and desire to work alongside life scientists Fabrication skills eg. 3D printing, CNC milling, laser milling Microfabrication experience a plus Ability to work unsupervised and with a minimal level of engineering infrastructure Strong communication skills and a collaborative mentality Good level of manual dexterity

We are currently looking for a Regulatory Labelling Contractor to join a leading Pharmaceutical company based in the North West London area. As the Regulatory Labelling Contractor you will be responsible for providing support in designing, implementing and maintaining processes for product information and product component labelling. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Regulatory Labelling Contractor will be varied however the key duties and responsibilities are as follows: 1. Approve change requests, artwork scope, check and ensure new version/product label is implemented with minimal bill of materials obsolescence 2. The Regulatory Labelling Contractor will assess and assimilate packaging change requests (change control) as a result of regulatory updates for example 3. Coordinate closely with internal business functions responsible for the various and new version / product introduction (Reg Affairs, Operations, Quality) 4. Proof-read texts and ensure alignment between source text and approved text for labels and leaflets ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Regulatory Labelling Contractor we are looking to identify the following on your profile and past history: 1. Relevant degree in a Scientific discipline 2. Proven industry experience in Labelling and Regulatory Affairs 3. A working knowledge and practical experience with document management applications Key Words: Labelling / Regulatory Affairs / RA / Regulatory / Artwork / Design / Pharmaceutical / SOP's / Standard operating procedures / Reg Affairs / London / Science / Document Management 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.

Junior Site Chemist (Chemistry Graduate, Mon - Fri) £20'000 - £23'000 + Overtime + Training + Progression + Excellent Benefits Package Ilkeston, Derbyshire (Commutable from: Derby, Nottingham, Chesterfield, Sutton in Ashfield, Mansfield) Are you a Chemistry graduate, looking for a hands on Site Chemists role, with a highly innovative company who will provide full training and structured progression? On offer is an outdoors, day's based role where you will receive on the job training from industry experts to allow you to progress in to a Senior Site Chemists role. This is an excellent opportunity to join this forward thinking market leader as they continue to expand and develop cutting edge solutions with in a growth industry. This is a varied role where you will be based outside, in an industrial environment. You will be responsible for input control, checking and treating incoming waste with occasional laboratory work. This role would suit a Chemistry Graduate looking for a hands on role with a rapidly expanding business who will provide full training and future career opportunities. The Role: *Junior Site Chemist (90% outside, 10% lab based) *Input control, checking & treating incoming waste, process authorisation and lab work *Full on the job training and external courses The Person: *Chemistry graduate (NVQ/ HNC/ HND/ Degree qualified) *Looking for a hands on, outdoors, days based role *Wants training and career development RTR89005 Please click "Apply" or contact Sam Dufosee at Rise Technical Recruitment if this role is of interest Chemist, Chemistry, Site, Industrial, Science, HNC, HND, NVQ, BSc, Degree, Graduate, Technical, Chemical, Engineer, Laboratory, Lab, Waste, Recycling, Industrial, Derby, Nottingham, Chesterfield, Sutton in Ashfield, Sheffield, Ilkeston, Burton upon Trent, Mansfield, Long Eaton, Loughborough, Matlock, Newark on Trent, Hucknall, Mansfield, Alfreton

Pharmaceutical Development Scientist, South Wales, £30-£35k E xcellent Pharmaceutical organisation with a multi-site group and excellent systems for employee development and training. Essentially we are looking for experienced Pharmaceutical professionals from Formulation or Process Development ideally with experience in Quality-By-Design & OR Formulation Development. This role will provide career development in formulation & Process Development within the pharmaceutical industry. Role of Pharmaceutical Development Scientist: Technical Transfer and scale up experience OR study related activities in Pharmaceutical NPI/Process Development Formulation Development for small molecules. Knowledge of cGMP Studies in Quality By Design (QBD) and/or DOE (Design of experiments) for the design of pharmaceutical experiments and projects. Please apply to be considered immediately

A Pharmacovigilance Assistant is required to support the PV department at a specialist pharmaceutical company. Based in Wiltshire, the company's products include prescription medicines, OTC, cosmetics, and medical devices. You will work in a busy PV department predominantly processing Individual Case Safety Reports (ICSRs) using ARISg as well as supporting the PV Manager where required. You will need to have proven workload management to ensure smooth running of the department when there is a heavy workload. This is a great opportunity for someone looking to join the pharmaceutical industry with a company that has a proven track record of bringing people in and train them up. You can definitely expect a rewarding career here. A life science degree or equivalent is essential. You do not have to possess current experience of PV but should have a good understanding of what a PV department does.

Lead Pharmaceutical Development Scientist, South Wales, £30-£35k Excellent Pharmaceutical organisation with a multi-site group and excellent systems for employee development and training. Essentially we are looking for experienced Pharmaceutical professionals from Formulation or Process Development ideally with experience in Quality-By-Design & OR Formulation Development. This role will provide career development in formulation & Process Development within the pharmaceutical industry. Role of Lead Pharmaceutical Development Scientist: Technical Transfer and scale up experience OR study related activities in Pharmaceutical NPI/Process Development Formulation Development for small molecules. Knowledge of cGMP Studies in Quality By Design (QBD) and/or DOE (Deisgn of experiments) for the design of pharmaceutical experiments and projects. Please apply to be considered immediately

Microbiology Technician Pharmaceutical industry Around £34,000 pro rata Based in Liverpool Due to an increase in workload our Pharmaceutical industry client is looking to appoint a Microbiology Technician on contract until the end of June 2020. There is a possibility of extension and potential permanent roles in the future for the successful candidates. You will be required to work a 4 on 4 off day shift pattern of 8.00am to 7.00pm (11 hours). Duties: To perform QC laboratory tests on in-process, intermediate and finished products. Tests regularly include TVC, WFI, Bioburden testing, LAL testing and Environmental Monitoring. To participate in ad hoc studies such as technical/validation studies, and provide technical expertise and advice around specific tests in troubleshooting. Qualifications and Experience: Minimum qualified to BSc level in Microbiology or a related subject is essential. Experience of working in a Pharmaceutical environment to GMP within a Microbiology laboratory environment. Experienced in the relevant testing discipline within the Pharmaceutical industry Experience of Quality Control testing techniques. Awareness of test and equipment validation Knowledge of continuous improvement and root cause analysis techniques For further details and to apply please contact Johnathan Miller at Scantec on johnathanm (at) scantec. co. uk and 0151._ 666._ 8925. Scantec Personnel Limited is acting as an employment business and an employment agency. For contract or interim roles (and unless otherwise stated), all pay rates stated are on a Limited Company basis. Due to the high volume of applications Scantec receives it is not always possible to acknowledge every application. Shortlisted applicants will be contacted within 28 days. If you don't hear from us within 28 days your application has not been shortlisted at this time, to be considered for future vacancies please register with us on our website.

Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing. In 2018, Eurofins generated 4.2 billion Euro proforma turnover in 800 laboratories across 47 countries, employing about 45,000 staff. Job Description Please note that the working hours for this role are as follows: 16 hours per week over 2 days. A role at Eurofins is challenging and varied each and every day. In return we offer a competitive salary and benefits package to reward our great people for all the hard work they do. This role is to provide an independent review of BRCGS Audit reports completed by EFSS auditors. To review against BRCGS requirements for report writing, check content and ensure consistency, accuracy and relevance to the client and the site audited Technical review of BRC draft audit reports received from the Certification Coordinator or Administrator, written by Auditors. Checking of reports to include spelling, grammar, format, detail and clarity of detail of all reports and level of accuracy /compliance to BRCGS report standards in required timeframe. Communication with Auditors to discuss queries. Communicating major issues to the Certification Coordinator and/or Certification Manager (depends on nature of an issue). Liaison with the Certification Coordinator once reports are checked and approved. Saving of all correspondence and checked reports on M:Drive in a relevant clients file. Completion of relevant part of control sheet. Maintain good communication with certification team. Undergo any required ongoing training in relevant to the job standards. Qualifications Degree in Food science or equivalent is essential Experience in Food manufacturing, within a technical systems role preferably Previous experience in similar role Senior management level in Food manufacturer is desirable Completion of training, relevant to the role standards IT literate (Word in particular) High attention to detail Excellent communication skills - both verbal and non-verbal Able to work independently yet still as part of a team Additional Information In return you can expect a competitive salary, 25 days holidays plus bank holidays, good team and working environment, life assurance and other benefits such as Perkbox, car parking and employee assistance programme. Your Data As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Closing Date Due to the high volume of applications we receive please be aware that if you do not receive a response within 4 weeks of the vacancy expiry date unfortunately, on this occasion your application has been unsuccessful.

Organic Chemist Hertfordshire Permanent & Full Time role Excellent Salary & Benefits Reed Scientific are currently working with a leading Biotech based in Hertfordshire who are currently going through a period of growth and because of this are looking for a PhD level Chemist with a strong background within Synthetic or Organic Chemistry experience to join their Chemistry team. Duties of the role will include: Devise and carry out Synthetic Medicinal Chemistry experiments and apply analytical and purification techniques Maintain and develop a high level of knowledge within technical R&D related to Organic/Synthetic Chemistry Communicate technical knowledge to both internal and external stake holders Key skills/experience required: PhD qualification - Medicinal, Synthetic or Organic Chemistry Minimum 2 years post doc experience (academia/industry) Possess strong analytical and purification experience including HPLC, LC-MS & NMR If this sounds like a role of interest, then please follow the link to apply, or contact the Reed Scientific office in Cambridge for more information.

Background REED Scientific have an exciting opportunity for an Interim Technical Manager to work within an independent, third generation, family-run business. The business works directly with locally, contracted farmers and produce a variety of dairy products which are delivered to wholesalers, retailers and direct to the doorstep. They are an award winning business, who pride themselves on offering real service to the customer and high quality products. The Role The main responsibilities and functions of this role include: - Direct Quality Assurance operations for the company - Develops and controls quality programs - Monitor the production departments' conformance with quality systems - Understand, establish and audit quality safety systems associated with the production of a safe product. - Audit and manage company operations to ensure legal compliance and to provide due diligence. - Maintain and develop HACCP and process control systems and documentation in line with company and customer requirements. As a senior member of the management team you will also work together to implement improvements in the business practices and operations. - Technical support during the NPD process including the approval of new suppliers, product, process in order to meet business strategy of developing added value products - Source and manage chemical stocks - Resolve customer complaints, ensuring target levels are achieved and improved. - Oversee the operations of the laboratory. - Environmental monitoring and reporting to meet compliance regulations. The Requirements - Degree/HND (or equivalent) in a food related subject. - Experience of working within FMCG with the BRC. - Internal and external auditing experience. - Sound technical and food safety knowledge. - Report writing, clear and concise presentation of information. - Excellent attention to detail with clear focus on end results. - Excellent Communication skills and strong negotiation skills. - Personal integrity and an ability to work independently. - Great deadline management and problem solving skills are also essential. They are committed to training and giving you the skills and abilities to carry out your role, providing progression and opportunities, allowing you to build a long term relationship with the company.

This small, innovative company is developing a range of low-power navigation products and is seeking a Graduate Engineer who can bring enthusiasm and new ideas to the design process. You will have an excellent academic record, including good A Levels and a 2...... click apply for full job details

JOB TITLE: Draughtsman / Design Engineer / Mechanical Designer / Project Engineer COMMUTABLE FROM: Hull, Anlaby, Barton upon Humber, Beverley, Brough, Cottingham, Hessle, Goole, Grimsby, Market Weighton, Scunthorpe, Selby, Willerby, York SALARY AND BENEFITS: £25-35k DOE 1.5x Overtime rate Holidays increasing with service An opportunity to work for a company who work with blue-chip clients...... click apply for full job details

My client are seeking an experienced Design Manager for initially 3 days per week to assist them with design and technical issues on a commercial refurbishment project in Covent Garden, Central London. The project is a commercial warehouse refurbishment consisting of cut & carve elements and the works are approximately £8m in value...... click apply for full job details

Job Title: Project Design Engineer Salary: £38,000 - £45,000 Location: Uttoxeter Our client, based in Uttoxeter, are looking to recruit a Project Design Engineer on a permanent basis to provide design engineering support...... click apply for full job details

Head of UX Design - London My client are a late stage start up whose presence is within the music/events industry, in over 420 cities around the world. They're looking for a Head of UX Design & Research to manage their growing UX team!..... click apply for full job details

UX Design Manager * Central London * Permanent * Salary / Bonus / Benefits My client, a leading global Asset Management company, based in central London are seeking a user experience designer who has previously created a UX function that supported multiple development teams across different locations, enabling multiple teams to develop striking, bright applications, which encourages users and in..... click apply for full job details

Zebrec are delighted to offer this role as AV SYSTEMS DESIGN ENGINEER working for our client who is a reputable & leading provider of professional services to their industry of Audio Visual Systems Integration. Snapshot of Role, Responsibilities & Skills for the AV SYSTEMS DESIGN ENGINEER: Experience and practical knowledge of the installation and use of Lighting, Sound, AV systems and syste ..... click apply for full job details

Revit CAD Technician - Hatfield Excellent Salary, 40hr working week, 23 days holiday increasing to 25 with 3 years' service, Private Medical Insurance, Life Assurance, Income Protection, Share Scheme plus more. Key skill areas: AutoCAD 2D, MHE Engineering, Architectural, Structural, 3D CAD (Revit, Solidworks, Inventor), Sketchup The Company This growing company designs and develops innovative..... click apply for full job details

THE OPPORTUNITY Cutting-Edge: You will be developing state-of-the-art airborne electronic sensor systems for the most advanced fighter aircraft ever to be made. Innovative: You will be involved with novel product development and emerging technologies that have been supported by Leonardo's multi-million pound annual investment in research and development...... click apply for full job details

Computing Teacher Requied for Prescot School part of The Heath Family Trust The Supply Register are delighted to be working exclusively for recruitment with The Prescot School, An Academy of Heath Family Trust. Requirements for Leadership, Teaching and Support Staff are presented to The Supply Register to source and connect the right candidate for the role...... click apply for full job details

Process Development Technologist My client a successful and well respected food manufacturer in Leicester are seeking a Process Technologist to join their Technical department, assisting in the launch of new products to specification, legal, quality and operationally sound processes. Key Responsibilities Working within NPD Managers to manage the process from kitchen handover to post launch review...... click apply for full job details

Design Manager (Leading Main Contractor) | £70,000 - £80,000 + package | Permanent | West London One of the UK's leading Main Contractors have an excellent opportunity for a Design Manager to join them on a permanent basis, based out of their West London region...... click apply for full job details

Diagnostic/Master Technician Vacancy - Watford Area Location: Watford Ref: OC8324 Salary: Basic up to £38k plus bonus, OTE £45k+ plus overtime and company benefits. (salary and bonus are subject to skill set, experience and/or any brand accreditation) Hours: Mon-Fri 8am-5...... click apply for full job details

Overall Purpose The role will be responsible for the management of design related issues across multiple sectors, from Pre-construction through to the Construction Stages of individual projects...... click apply for full job details

Packaging Account Manager Location: West Yorkshire - Leeds & Bradford Salary: DOE Company: A leading agency specialising within packaging, branding, marketing and print. Role: Responsible for managing projects from initial concept to completion - through design process to production whilst ensuring an exceptional client service...... click apply for full job details

Maths Graduate Teaching Assistant Have you recently qualified with a 2:1 or 1 st class Maths degree? Are you wanting to pursue a teaching career, but need more experience within the classroom before jumping into full time teacher training? Why not gain 'outstanding' experience while getting paid for it at the same time, could there be a better start to your teaching career?..... click apply for full job details

Biomedical Field Service Engineer - North London Package - up to £38,000 per annum / company car / pension / overtime opportunities / private healthcare / 25 days holiday / door to door pay My client is an independent provider of medical equipment; delivering first-class service standards to the NHS, Emergency and Rescue Services, the Private Healthcare sector and others...... click apply for full job details