LSC have a great contract opportunity for a QC Team Lead to join a Bray based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 5+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Ensure that the QC lab follows Good Laboratory Practice/Good Manufacturing Practice. Implement and maintain standards of GLP practice consistent with regulatory expectation and cGMP.
- Responsible for all aspects of guidance of a team of QC analysts/technicians, including performance management and the execution of business processes to a high standard as monitored.
- Support your team and help them to perform to a high standard, in the achievement of the company and department goals.
- Ensure that Production, QA, Planning, Shipping and support departments receive a quality service through meeting scheduled target release dates and compliance standards.
- To perform an investigation into any non-conformance, instrument malfunction, accident or other abnormal occurrence.
- Validation, operation, maintenance, calibration and troubleshooting of laboratory instruments.
- Approval of relevant QC documentation
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- BSc. (minimum) in science or a related discipline
- 5 years' experience in an analytical lab preferably with supervisory responsibilities.
- Technical experience of GC / HPLC Analysis required.
- Experience with continuous improvement plans within the QC environment.
- Experience managing, motivating and leading a team of analysts
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Gráinne Hodnett on 021 4777 329 if you have any more questions about this opportunity!
