Do you have experience in the analysis of biomolecules? A background in the validation of analytical methodologies for the testing of biological products? A fantastic opportunity to join a progressive company that genuinely values its employees is now available.
Roles and Responsibilities
Write procedures for analytical methods, equipment, processes to the required quality for cGMP compliance.
Support the optimization, phase appropriate validation and/or technical transfer of developed methods for cGMP testing.
Execute method qualification and validation protocols and assist in writing the associated reports as required.
Perform testing of utilities, raw materials, process development, in process, product release and stability to ensure delivery on time, on budget and in compliance with the established quality standards.
Lead the management of samples for projects assigned to them. Responsible for interpreting and analysing experimental results and communicating them effectively via study reports and presentations to Snr Manager, Analytical Sciences.
Support the installation and validation of analytical equipment by writing and executing equipment validation documentation including but not limited to URS, trace matrix, IOQ, SOP’s, protocols and reports in line with quality procedures and guidelines.
Qualifications and Experience
BSc science graduate (or equivalent) with biopharmaceutical or pharmaceutical experience
Experienced in the analysis of biomolecules and writing procedures, protocol and reports
Working knowledge of analytical techniques including but not limited to Electrophoresis (SDS-PAGE, Western Blot, IEF), Chromatography (SE-UPLC, RP-HPLC, AEX, HILIC), Immunoassays (ELISA, Potency, HCP)
Please forward your CV to cameron.miskin@nextphaserecruitment.com or phone 0044 1403 216216 where we would be happy to tell you more about this exciting opportunity.