Project Manager

We are seeking an experienced Project Manager to support a major pharmaceutical manufacturing ramp‑up within CPMF (Centralised Pharmaceutical Manufacturing Facility). This is an 18‑month onsite role dedicated to driving technical, engineering, and operational projects in a highly regulated GMP environment. You will work closely with operations, engineering, quality, and leadership teams to ensure manufacturing capacity increases, compliance risks are mitigated, and critical systems are implemented effectively. Success in this role requires strong project leadership, deep understanding of pharmaceutical operations, and the ability to coordinate complex technical workstreams.

What You’ll Do

• Lead multiple pharmaceutical manufacturing and engineering projects supporting the CPMF ramp‑up
• Ensure project plans align with GMP requirements, operational readiness, and technical design needs
• Develop tools to track project progress and proactively resolve issues across manufacturing and engineering
• Monitor performance against quality, reliability, schedule, and cost targets
• Support resolution of technical and non‑technical issues throughout the project lifecycle
• Coordinate contractor activity in collaboration with Engineering to ensure compliance and safety
• Provide timely updates to sponsors, leadership, and end users within operations and quality
• Support budget development and assess project changes impacting pharmaceutical production timelines and costs

Key Focus Areas (Pharmaceutical Manufacturing)

• Parallel Manufacturing: Lead capacity‑increase initiatives to meet site pharmaceutical production needs; assess freeze dryer and autoclave capacity within the manufacturing process
• Clean‑in‑Place (CIP) System: Implement a new automated CIP system to replace manual cleaning, supporting GMP compliance and contamination‑risk reduction
• Module Re‑Piping (SCRI‑IS Findings): Review and update manufacturing piping to reduce contamination risks and ensure compliant facility design
• Training Plan: Develop and manage a site‑wide CPMF training program for GMP‑aligned operations

What You Need

• Strong project management experience, ideally within pharmaceutical, biotech, or other GMP‑regulated manufacturing environments
• Experience with facility engineering design and technical operations
• Ability to lead and influence cross‑functional teams including engineering, quality, and manufacturing
• Excellent communication skills for translating technical and GMP requirements across stakeholders
• Advanced problem‑solving ability with strong technical judgement
• High collaboration, strong teamwork, and sound decision‑making under regulated conditions

If interested please apply!