GMP & Compliance Project Manager in Radiopharmacy (m/f/d)

In this role you will coordinate and execute GMP-related projects across manufacturing, cleanroom, and lab settings, ensuring compliant introductions of new facilities, equipment, and processes. You will act as a key interface among Operations, Quality Assurance, Engineering, and external partners to support regulatory alignment. You will contribute to qualification, validation, risk assessment, and CAPA activities, while participating in inspections and audits. You will operate in a fast-growing radiopharmacy environment focused on PET diagnostics and continuous improvement. This is an opportunity to shape GMP-driven expansion at a market-leading company with international reach.

• flexible working hours
• job ticket / travel allowance / company bicycle
• proximity to public transport
• free drinks
• company events
• allowance for fitness and sports activities

• Plan, coordinate, and implement GMP-related projects in manufacturing, cleanroom, and laboratory environments
• Ensure GMP-compliant project execution per regulatory requirements and industry standards
• Prepare, review, and maintain qualification, validation, and project documentation
• Participate in regulatory inspections and audits
• Support risk assessments, change control processes, and CAPA activities
• Assist in commissioning and qualification of new equipment, facilities, and processes

• Several years of professional GMP-regulated environment experience
• Solid knowledge of current EU GMP guidelines
• Experience in qualification and validation projects
• Initial experience handling radioactive materials and compounds
• Structured, self-directed, and solution-oriented work style with strong communication and organizational skills

• communication
• coordination
• organizational skills
• GMP compliance
• qualification and validation
• regulatory inspections and audits