For our client, we are seeking an experienced Technical Project Manager to support CAPEX and optimization projects within a highly regulated GMP environment. In this role, you will lead cross-functional project teams, coordinate with internal and external stakeholders, and ensure timely and compliant delivery of all project activities.

This position plays a key part in driving Annex 1–related improvements across sterile manufacturing operations.

Start Date: ASAP

Contract: Until December 2026 (extension possible)

Workload: Full-time

Your Responsibilities:

• Lead, plan, and coordinate all project-related activities across multiple functional areas.
• Act as the primary point of contact for internal stakeholders and external partners.
• Ensure all project deliverables are developed, reviewed, approved, and executed according to schedule, budget, and quality expectations.
• Drive compliant project execution in GMP-regulated and capacity‑constrained environments.
• Support and execute CAPEX and optimization initiatives, including but not limited to:
• Improving sterile filtration processes (e.g., Point of Fill Filtration).
• Developing and implementing an electronic documentation system for Grade A interventions.
• Sealing and infrastructure optimization in Grade D areas.
• Optimizing transitional spaces (MAL) to meet Annex 1 requirements.

Your Profile:

• Bachelor’s or Master’s degree in Mechanical, Electrical, Process, Chemical Engineering, or equivalent.
• Minimum 5 years of experience in technical project execution within GMP‑regulated environments (pharma, biotech, life sciences).
• Hands-on experience with FMEA, technical troubleshooting, and cross-functional project coordination.
• Fluent English and German (spoken and written).

Solid understanding of:

• cGMP
• EU Annex 1
• Engineering documentation
• Strong ability to interpret and apply regulatory expectations in daily project work.