LSC have a great contract opportunity for a QA Validation - Technical Writer to join an innovative and rapidly growing Biopharmaceutical company in Limerick. The facility is responsible for the production, packaging, labelling and delivery of biopharmaceutical medicines for global markets. The company currently markets medicines for various diseases and has a rich pipeline of products.
If you have experience in QA Validation activities and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Experienced Technical writer o Experience in Deviation and investigation writing
- Experience in Validation specifically CIP/SIP and continuing validation
- Experience in assessment of CIP/SIP issues during study runs and closeout of deviations
- Experience in KAYE validator reporting review beneficial
- Capable of managing a large program, so project management skills would be necessary
- An understanding of how manufacturing, CIP and SIP Validation equipment works
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Execution, review & approval of SIP/ CIP and continuing validation protocols and closure
- Extensive experience on writing and approving Deviations
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 Sarah Ninan if you have any more questions about this XXXXX opportunity!
