LSC have a great contract opportunity for a QA Specialist with a large biopharmaceutical company based in Cork.
If you have 3+ years of relevant experience in a GMP environment related field and a BS and ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Participates in developing Standard Operating Procedures and writes and/or implements changes to controlled documents to ensure quality objectives are met.
- Participates in reviewing and approving Standard Operating Procedures (SOPs)/other types of controlled documents.
- Performs QA review and release of primary and secondary packaging components.
- QA Review and approval of GMP Deviation investigations and CAPAs
- QA Review and approval of Master data and recipes required for operations
- Maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs).
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- BSc in Science or Engineering
- 3+ years of relevant experience in a GMP environment
- Demonstrates basic knowledge of OPEX Lean tools and root cause analysis tools used for identifying and correcting deviations.
- Demonstrates audit and investigation skills, and report writing skills.
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 Grainne Hodnett at +353 214771329 if you have any more questions about this opportunity!
