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 Troubleshooting.
- 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 a 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, and 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
