LSC has a fantastic opportunity for a CQV Lead to join a large multinational project in the biopharmaceutical industry in Denmark.
If you have experience on high value CAPEX projects working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- CQV Lead Engineer with responsibility for creating and documenting CQV procedures, CQV strategy and grouping strategy.
- Review of all GMP generated documentation.
- Point CQV person for Vendor review for Vendor Packages.
- CQV SME for process equipment and supporting utilities etc.
- Lead CQV effort for schedule review and readiness.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Minimum of 10 years' experience including experience with design and construction projects for Drug substance biopharmaceutical manufacturing facilities.
- Experience with complex projects and within a CQV Lead capacity taking responsibility for setting the strategy and direction on a project.
Apply via this advert or contact Cian Marnane at 021 4777329 if you have any more questions about this role!
