Job Title: Freelance CQV Engineer
Start Date: March 2025
Contract: 12 Months
Location: Denmark - Onsite
EPM Scientific is partnering with a leading pharmaceutical company to find an experienced CQV Engineer to be part of their commissioning, qualification, and validation of pharmaceutical manufacturing systems.
Overview:
The company has finalized most facility and equipment designs, along with factory acceptance testing (FAT). On-site, preparations are underway for the installation of process equipment, planning validation activities, and all tasks necessary for operational readiness.
Responsibilities:
- The Associate WPO will report to the WPO Downstream and collaborate closely with colleagues in Downstream engineering/operational responsibilities, local production specialists, IT/Automation specialists, and various project management stakeholders.
- The role will focus on planning, coordinating, executing, and following up on equipment installation, SAT, CQV testing, and operational readiness activities.
- The Associate WPO will work in collaboration with the downstream team, CQV team, Site Construction Management, Suppliers, and Engineering Partners to ensure timely and efficient delivery of tasks.
Key Skills & Experience:
- Proven experience as a lead WPO/PM within the Biopharma industry.
- Strong leadership qualities with a positive, collaborative, and proactive team-oriented mindset.
- Expertise in managing cross-functional teams and driving results in complex, fast-paced environments.
How to Apply:
If you're a good fit, 📩 let's connect! DM me or share a time to chat!
