A multi-national Pharmaceutical client is looking for a CQV Manager for the commissioning of a multi-million Euro pharmaceutical construction project in Denmark.
If interested, please reply with your most updated CV and references.
Details:
- Position: CQV Manager
- Location: Denmark
- Working arrangement: Freelance
- Contract: 12+ months
- Mobilisation: Immediate
- Rate: Negotiable (Based on experience)
Responsibilities:
- Lead and oversee all Commissioning, Qualification, and Validation (CQV) activities during the project commissioning phase
- Develop and execute CQV strategies, plans, and protocols in line with GMP requirements
- Ensure compliance with regulatory standards and industry best practices
- Coordinate with engineering, quality, and project teams to ensure seamless system handover
- Manage FATs, SATs, IQ/OQ/PQ activities across systems and equipment
- Review and approve CQV documentation and reports
Requirements:
- Pharmaceutical experience (mission critical)
- Experience working on commissioning phase of large-scale projects
- Experience leading team of 20+
- Right-to-work in EU (EU Passport)