• Junior QA/Administration Officer/Archivist 8/22/2017 12:00:00 AM

    Salary: £20000 Location: WELWYN GARDEN CITY

    Client are a successful, expanding and GLP/GCP compliant specialist contract laboratory that perform quantitative analysis of drugs, metabolites and endogenous biomarkers in biological fluids and other matrices to support pharmaceutical and academic R&D. Essential:- + Experience of performing quantitative analysis preferably using Sciex Triple Quad systems and Analyst software + Readiness to perform administrative tasks contributing to the smooth run of the laboratory + Experience of working to support GLP/GCP studies + Performed quality control review of data + Reviewed and used SOPs + Ability to quickly to adapt to new processes + A degree in Chemistry or Biochemistry Microsoft Office software proficiency + History of working as a team player Desirable:- + History of working at a similar position + Has conducted or experienced quality audits + Has conducted paper and/or electronic data archiving + Understanding of CAPA and risk assessment + An understanding of the role of quantitative analysis in the drug development process + Experience with Vision Publisher and NuGenesis software + Willingness to undertake any task requested to help achieve company goals + Excellent communication skills IT proficiency Involvement with RQA For this position, my client are looking for an organised, self motivated individual with an excellent attention to detail to either join us full time or work flexible part-time (2-3 days)during the week. Although this individual will not be expected to analyse samples, it would be useful to have experience performing quantitative analysis by LC-MS in a GLP/GCP environment. We are happy to facilitate training for the right person, but please do bear in mind that due to the nature of the work carried out at ABS, it is a requirement that the candidate is a NON-SMOKER in order to prevent contamination of our facilities. Salary £20,000 per annum

  • QA Compliance Officers:- 6 month FTC 8/22/2017 12:00:00 AM

    Salary: £24000 Location: SOUTHPORT

    My Client manufacture and supply branded and own label healthcare pharmaceutical products for a number of therapeutic areas including cough, cold and pain relief for the UK and Export market. They are looking for 2 QA Compliance Officers (6 month contract) reporting to the Senior QA Compliance officer/ Working hours are 08:00 to 16:30, Monday to Friday, 40 hour week. We are looking for candidates with scientific degrees and ideally 12 months of experience in QA though recent graduates are also welcome to apply! Requirements - Scientific Degree, Experience working in a QA function in a Pharmaceutical company, Computer literate and ability to use Microsoft office. Experience in working in the areas detailed below is preferable, on the job training will be provided. 1. Complaints Coordination and answering non-PV complaints in collaboration with QA Manager/ QP. 2. Facilitate project to amalgamate PPDRs into QA IR into one deviation system to remove current “two tier” system 3. Entry of CAPAs from multiple sources- Quality Deviations, Audits (internal/external), Inspections, APRs, PV Deviations onto Tracker. Provision of regular metrics to Quality Circle. 4. Hold regular meetings with CAPA owners to ensure CAPAs closed within specified timelines. 5. Initial QA review of Raw Material Documents generated by Goods in lab against Pharmacopoeia. 6. Review and preparation of packaging/ finished product specifications. 7. Preparation of Raw Material risk assessments (completion of outstanding Excipient RA’s and renewal of existing API/Excipient RA’s as they expire) 8. SOP and QAF Revision 9. KPI Preparation 10. Control/issuance of forms (data integrity) 11. Issuance of Packaging Sheets 12. Training coordination 13. Cover for packaging component sampling. Salary £21,000 - £24,000 pro rata If youre interested in this position, please send your CV to

  • Microbiology Manager 8/17/2017 12:00:00 AM

    Salary: £0 Location: CAMBRIDGE
  • Senior LC-MS/MS Method Development Specialist 8/16/2017 12:00:00 AM

    Salary: £45000 Location: WELWYN GARDEN CITY

    Based in Welwyn Garden City, my client are a highly accredited contract research organisation who specialise in the quantification of biomarkers, metabolites and drugs within both biological and non-biological samples. They are currently expanding and are looking for a senior LCMS chemist. Ideal candidates will have the following skills; + Experience performing quantitative analysis for biomarkers or drugs present in biological matrices in support of clinical trials. + Expert at developing and validating quantative LCMS methods to EMA/FDA guidelines. + Experience of extracting and analysing samples using 96 plates. + Ideally experience of Sciex Triple Quad systems and software. + Work to GCP/GLP standards. Salaries for the positions are expected to be around 45k for the right candidate.

  • Analytical Chemist 8/10/2017 12:00:00 AM

    Salary: £0 Location: RUSHDEN

    Analytical Chemist – Chemistry My Client is a premier R&D service provider supporting the life science industry. Founded in 2003, they have established diverse drug R&D service capabilities, ranging from synthetic, medicinal and analytical chemistry, biology, DMPK, pharmacology, drug safety assessment, radiochemistry and isotopically labelled metabolism, chemical & pharmaceutical development to clinical development, including applications of 14C microtracer AMS technology. With operations in China, US and UK staffed by over 4,500 employees, they have an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China. Due to recent expansion they are currently looking to recruit a Analytical Chemist facility within Chemistry. You will have a sound basic theoretical understanding of a range of analytical techniques primarily chromatographic and spectroscopic. After a structured period of training the successful candidates will be required to carry out analyses on a diverse range of chemical compounds, generate and provide first line interpretation of the resulting data and preferably be able to defend the interpretation to senior QC analysts and internal Clients. You will be expected to produce analytical reports compliant with QA systems. You will ensure that the instrumentation under your charge is maintained, operationally available, as far as is reasonably practicable at all times, and that there is an adequate supply of materials to meet QC operational requirements. You will have a can do attitude always looking for ways to support the business outside of your immediate job specification. Essential requirements • Degree in Chemistry, or relevant experience • Good theoretical grounding of chromatographic and spectroscopic techniques • Good written and verbal communication skills • Computer literate • Ability to work with minimum supervision and as part of a team • Conscientious and meticulous in laboratory and written work • Good time management skills and ability to work to tight deadlines • Proven ability to problem solve • Willing to get involved with new ideas and initiatives Desirable requirements • Experience as a practising analyst, particularly with chromatographic and spectroscopic techniques. • Experience in data evaluation using spreadsheet and statistical tools. • An appreciation of quality/regulatory standards and quality systems - in particular the relationship of the MHRA with the pharmaceutical industry. The position is full time and permanent. Hours of work are 37.5 per week Monday – Friday. Annual holiday entitlement is 23 days a year plus Bank Holidays. The company operates a contributory pension scheme, life assurance and a flexible benefits package.

  • Method Development Scientist 8/8/2017 12:00:00 AM

    Salary: £0 Location: SKIPTON

    My client are an independent contract analytical laboratory servicing the pharmaceutical and healthcare industries. They are going through a major expansion and are looking for a number of Method Development Scientists to join their team. The ideal candidate will have at least 3 years experience within HPLC method development and will have worked to ICH Guidelines. Experience with techniques such as LC-MS, GC-MS and ICP-MS is essential. Previous analysis of Inhalation Products would be an advantage. You will benefit from: +Competative Salary +Bonus Package +Pension Scheme

  • Head of Quality Assurance 8/7/2017 12:00:00 AM

    Salary: £0 Location: NOTTINGHAM

    Head of Quality Assurance This is a superb opportunity to join a small, fast-growing company, offering formulation, development, and manufacturing services to the pharma and biotech industries. The role is based at our facility within BioCity, close to the centre of Nottingham. The company is looking to recruit a highly motivated Head of Quality Assurance, to design and implement a Quality Management System to support the establishment of a cGMP manufacturing capability within our BioCity facility. Key responsibilities will include – • Designing and implementing a QMS for the company’s cGMP activities, which complies with the relevant regulatory requirements, and meets the needs of the business. • Ensuring that all of the company’s cGMP activities are carried out within the framework of the QMS. • Fronting regulatory inspections and client audits. • Designing, implementing, maintaining and monitoring QMS systems for change controls, CAPA management, internal and external audits, supplier/subcontractor approvals, and quality issues/investigations. • Working with the GMP production manager to define, document, and implement cGMP manufacturing procedures (facility, equipment, and operations) in compliance with regulatory requirements. Qualifications and experience • Significant experience of managing quality systems in the pharmaceutical industry. • Thorough knowledge of the regulatory framework around cGMP and the manufacture of investigational medicinal products • Experience of managing change and implementing systems and procedures across an organisation • A relevant degree, ideally in pharmaceutical or biological sciences • Experience of regulatory inspections and audits We Offer: • Competitive salary • Full time permanent position • Flexible working • Company pension plan • 33 Days annual holiday (including bank holidays) Applicants must have the right to work in the UK upon being offered employment.

  • QA Manager 8/4/2017 12:00:00 AM

    Salary: £0 Location: STAFFORDSHIRE

    My Client are a Biopharmaceutical Manufacturing Company in Staffordshire who specialise in the design of robust processes for their life science customers in the quality commercial, clinical and preclinical areas. They are looking for a Quality Assurance Manager that will be responsible for the day to day GMP Compliance at their manufacturing facility. This position will report to the Quality Director and will also work closely with the with the Operations and Project Management teams. Key Responsibilities Include but not limited to:- ++ Development and optimisation of the Quality Management System ++ Managing Quality System action closure ++ Being responsible for the site QA Team: coaching staff, line management etc. ++ Reviewing and approving quality documentation ++ Managing the supplier assurance and validation systems. Requirements:- ++ Previous Managerial experience ++ Relevant experience in a manufacturing or QA role ++ Possess a science degree or equivalent. Ideal candidates will have experience of biologics, though this isnt essential Salary:- £55k

  • Analytical Manager 8/3/2017 12:00:00 AM

    Salary: £0 Location: SHEPHERDS BUSH

    Based in London, my client is a global leader in specialist imaging working towards the understanding of disease and translational drug development. You will have- Minimum of BSc in Chemistry or other relevant subject with strong evidence of your analytical expertise Extensive experience in HPLC, GC, IC (LCMS would be beneficial but not essential) Strong people management skills Evidence of leading a team Due to company progression, they are looking for an experienced and time served Analytical manager. Reporting to the head of clinical chemistry, you will be responsible for leading a multidisciplinary team of 6 specialists with in a GMP facility, in analytical chemistry and microbiology. This position requires an individual to lead by example and demands someone with strong people management, technical expertise and effective communication skills. Excellent salary £45-£50k (dependant on experience) Great career progression options. If you have the right level of analytical skills and people management expertise please forward an updated CV to

  • Study Manager- E-Fate 7/31/2017 12:00:00 AM

    Salary: £0 Location: RUSHDEN

    Study Manager- E-fate- Metabolism Based in Northamptonshire my client is a fast growing CRO, providing services for the Pharmaceutical industry and they are one of the market leaders in specialist drug development Services A fantastic opportunity has opened up for a Study Manager. Main duties and responsibilities include Conduct and/or Study Direct metabolism studies for new product development based on global regulatory requirements The ideal candidate will have- Bsc in a life science subject Previous experience of conducting Metabolism/E-Fate studies in a GLP Experience of Study Directing Metabolism studies in the pharmaceutical or CRO industry is desirable Prepare study plans, amendments, file notes and deviations as required. Excellent salary (depending on experience) great benefits modern facilities. This is a rare opportunity to be involved with a successful and still growing company, that is oriented towards building long-term success for them and their employees. If you’re interested in the role contact Brian Lamont at North point today. 0161 932 8188


« previous 1 2 3 4 next »