Job Description

Testing of in process, stability and finished product samples. eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management.
Review and authorisation of Lab Data
Support Analytical Technical Transfer activity testing reports and documentation.
Document review/updates when required.
Equipment Calibration, Maintenance and Trouble Shooting.
Method Validation/Verification.
Training of QC Chemistry Laboratory colleagues.
Laboratory Investigation support
Laboratory Housekeeping and maintaining GMP standards.
Assisting in regulatory audits.
The successful candidate will:
• Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject.
• Have at least 5 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 team work skills.
• Proven track record of meeting deadlines.
• Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous