A fantastic opportunity has arisen for an experienced senior QC Analyst to join a busy analytical team within a leading biopharmaceutical company in South Dublin on a 12 month contract with the possibility of extension.
Responsibilities will include:
- 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.
Qualifications & Experience:
- Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject.
- 3 - 5 years relevant experience in a pharmaceutical/healthcare environment
- Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing is required.
- 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.
Top Skills:
- Significant xperienced in executing HPLC
- GMP lab experience essential, biopharmaceutical experience an advantage.
- Software experience in LIMS/LMES and Empower as this is used for execution of the HPLC.
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
