C&Q Engineer GMP Projects

Help deliver pharmaceutical capital projects from construction through this on-site assignment youll coordinate C&Q activities for facilities utilities production equipment and computerized systems in a GMP environment.

Your responsibilities

• Drive commissioning and qualification activities in line with project milestones GMP requirements and site procedures.
• Develop and maintain C&Q plans and schedules particularly for construction and qualification phases.
• Prepare review and approve qualification plans protocols reports and acceptance criteria.
• Coordinate colleagues contractors and stakeholders across Engineering QA MS&T suppliers and end-user teams.
• Support investigations change controls corrective actions and audit readiness.

Your profile

• Degree in Engineering Life Sciences or a related scientific discipline.
• At least 3 years of relevant experience in a pharmaceutical GMP environment.
• Experience in commissioning qualification or validation; exposure to capital projects or oral solid dosage manufacturing is an advantage.
• Strong planning communication and problem-solving skills with the ability to work independently and collaboratively.