LSC has a fantastic opportunity for a Downstream 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:
- Site has finalized most facility and equipment design and have moved into factory acceptance testing (FAT) in close collaboration with Suppliers and our engineering partners. On site, we are preparing to install process equipment, planning validation activities as well as all activities required for operational readiness.
- As an Associate WPO (Senior/Lead Downstream CQV Eng) you will refer to the WPO Downstream and collaborate closely with your colleagues of Downstream engineering-/operational responsible, local production specialists, IT/Automation specialists and also interact with a wide range of project management stakeholders.
- Responsibilities/tasks will focus on planning, coordination, execution and follow-up of equipment installation, SAT, CQV-testing and operational readiness activities, and deliverables in collaboration with other the downstream team, CQV team, Site Construction Management, Suppliers and Engineering Partners.
- Proven experience and skills as lead/WPO/PM within Biopharma. Leadership and positive, collaborative, proactive team-oriented mindset are key-words.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- 6+ years' proven experience from biopharma acting as a Lead/WPO/PM during Installation and CQV phases.
- Experience with complex projects.
- Strong leadership and communication skills
- Positive, collaborative, proactive team-oriented mindset.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold an EU/UK Passport to apply! Apply via this advert or contact Sarah Ninan at +353 214777329 if you have any more questions about this opportunity!
