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Hyper Recruitment Solutions
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Bioanalytical Manager

EastbournePermanent
£50,000 - £80,000 per annum
Job Reference: J5631947
Updated On: 28/07/2019
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Clinical Research Organisation, Contract Research Organisation, Contract Testing Organisation, MHRA QP License Holder, Science

Skills: Chemistry - Analytical - HPLC (Method Devlopment), Chemistry - Analytical - GCMS, Chemistry - Analytical - HPLC (routine), Chemistry - Analytical - Manager / Director, Chemistry - Analytical - Team Leader / Supervisor (5 staff max), Chemistry - Analytical - Instrument Validation, Chemistry - Analytical - Method Validation Only, Chemistry - Analytical - Method Development Only, Chemistry - Analytical - GC

Job Information

Role Overview

Hyper Recruitment Solutions are currently looking for a Bioanalytical Manager to join a leading Drug Development company based in the Eastbourne area. As the Bioanalytical Manager you will be responsible for building and operating a new Analytical Validation Laboratory, including developing/implementing analytical assays and for achieving/maintaining ISO/IEC and cGMP certification.

Key Duties and Responsibilities

Your duties as the Bioanalytical Manager will be varied however the key duties and responsibilities are as follows:

1. Lead operations of the analytical validation centre and management of a team of scientists.

2. Development and Implementation of ICP, GC/MS, HPLC and Microbiological Assays, Qualification and Validation of Instrumentation in the Analytical Section. Method Transfer from Analytical Validation Lab to Manufacturing Facility,

3. Implementation and maintenance of a robust QMS to maintain ISO/EC and cGMP certification.

4. Validation of R&D/Analytical Development data and QC Results of the manufacturing Site as well as reporting results to management and clients.

Role Requirements

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Bio-analytical Manager we are looking to identify the following on your profile and past history:

1. Relevant degree in a Life Science Degree

2. Proven industry experience in a Pharmaceutical cGMP/GLP environment.

3. A working knowledge and practical experience with ICP, GC/MS, HPLC and Microbiological Testing Methods.
4. Knowledge of FTIR/Karl Fisher techniques would be desirable.


Key Words: QC Team Leader / Analytical Team Leader / Analytical Scientist / Lead Analytical Scientist / HPLC / UPLC / GCMS / Method Development / Method Validation / SOP's / ICH / GMP/ Pharmaceutical / Pharma / Chemist / Scientist / Analytical / Research and Development / Quality Control Team Leader / Quality Control Lead / ICH / cGMP / Tech Transfer / Product Development / ICP / FTIR / Microbiology / Sterility / Karl Fisher / Technology Transfer / QC Manager / Analytical Manager / Bioanalytical / Bioanalysis / Method Development / Method Validation.

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.


Chris Sowden
Your Recruitment ConsultantChris Sowdenchris.sowden@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.