This is a 12-month contract with a view to extension.
It is an onsite role, 08:30 to 17:00, Monday-Friday .
Responsibilities Responsibilities include but are not limited to: Reagent preparation for the various HPLC methods Equipment Calibration, Maintenance and Trouble Shooting.
Training of new QC analysts on pH Calibration.
May require Testing of in process, stability and finished product samples.
eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management.
Laboratory Housekeeping and maintaining GMP standard Laboratory Investigation support Assisting in regulatory audits.
Qualifications Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject.
Have at least 3 years relevant experience in a pharmaceutical/healthcare environment.
Be very proficient in the use of Microsoft Word, Excel etc.
Have strong technical writing skills.
Be detail oriented, self-motivated with good troubleshooting and problem-solving abilities.
Be a self starter and capable of working on own initiative.
Strong teamwork skills.
Proven track record of meeting deadlines Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous Skills: HPLC Methods Equipment Calibration pH Calibration Testing Analytical Techniques