Senior Analyst - Laboratory Compliance

29 Apr 2019
27 May 2019
Chris Sowden
Contract Type
Full Time
Hyper Recruitment Solutions are currently looking for a Senior Analyst - Laboratory Compliance to join a leading Pharmaceutical company based in the Essex area. As the Senior Analyst - Laboratory Compliance you will be responsible for ensuring all instruments and equipment used in site laboratories complies with relevant regulations and guidelines to ensure continued GMP Compliance.


Your duties as the Senior Analyst - Laboratory Compliance will be varied however the key duties and responsibilities are as follows:

1. You will prepare initial qualifying documentation for new devices (single / complex computerized) as part of the qualification of new equipment and re-qualification after technical change/modification, this will include conducting qualifying tests and write subsequent reports and procedures for use and verification.

2. The Senior Analyst - Laboratory Compliance will schedule metrological checks of equipment, conduct first line maintenance of laboratory equipment and advise analysts in good instrument use practice. You will advise on the specification of user requirements and advise on the purchase of laboratory equipment/computerized lab systems.

3. You will plan and participate in reviews of computerized laboratory systems, manage the users of computerised laboratory systems and work with other departments to ensure lab equipment is maintained, serviced and calibrated.

4. Writing and updating Standard Operating Procedures, participating in internal/external audits and proposing necessary corrective actions, resolve non-conformances, implement change actions and CAPA's. You will maintain current knowledge of GMP and ensure H&S/COSHH guidelines are adhered to at all times.


To be successful in your application to this exciting opportunity as the Senior Analyst - Laboratory Compliance we are looking to identify the following on your profile and past history:

1. Relevant degree in a Life Science/Chemistry Discipline

2. Proven industry experience in a GMP/GLP compliant business in the Pharmaceutical Industry.

3. A working knowledge and practical experience with Good Documentation Management and experience working with a range of analytical techniques including HPLC, UV-Vis, GC-MS, IR.

Key Words: Analytical / Development / Validation / Specialist / Equipment / GMP / DQ / IQ / OQ / PQ / HPLC / UV-Vis / GC / FTIR / Computer System / Re-Qualifications / Qualification / Computerised Systems

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.

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