LSC has a fantastic opportunity for a CQV Lead to join an advanced global team in Denmark that promotes self-development, encourages collaboration, and fosters a learning environment. This is a chance for you to be a part of a fast-growing, multicultural company that has a compelling vision for shaping the future of medicine.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- CQV Lead Engineer with responsibility for creating and documenting CQV procedures, CQV strategy and grouping strategy.
- 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.
- Liaise with Project Director and Lead Scheduler in relation to schedule readiness and tracking.
- Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOC-IOQ Testing.
- Liaise with all Project Groups to ensure all Systems are managed appropriately for the entire Project Lifecycle.
- Key player for CQV in the Compliance cross functional team including Engineering, Automation and QA.
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.
- Demonstrated proficiency communicating and collaborating at a variety of levels with customers, local vendors, equipment suppliers and operations staff.
- Knowledge of Kneat, Veeva and EIDA system.
This is a fully on-site role.
Note: As this is a contract opportunity you will need to hold an EU Passport to apply! Apply via this advert or contact Sarah Ninan at +353 214777329 if you have any more questions about this opportunity!
