We are seeking a seasoned CQV Project Lead with strong expertise in managing commissioning, qualification, and validation projects independently. This role requires excellent analytical skills to understand technical requests, identify risks, and define project assumptions.
About the Role
The successful candidate will lead CQV projects from inception to completion, ensuring all deliverables meet regulatory and client expectations. Key responsibilities include:
* Project Leadership: Oversee commissioning, qualification, and validation activities, ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
* Bid Management: Analyze and interpret technical requests from clients, identify risks, and define key assumptions. Develop the best technical approach tailored to client needs.
* Risk Assessment: Identify and mitigate risks associated with equipment, processes, and systems to ensure seamless project execution.
The ideal candidate should have a minimum of 5 years of experience in CQV within the pharmaceutical or life sciences sector, a deep understanding of regulatory requirements, and exceptional communication and interpersonal skills. A Bachelor's or Master's degree in engineering, life sciences, or a related field is required.
Benefits
We offer a competitive salary based on experience, company car as part of the benefits package, opportunities for career development in a dynamic and growing international company, and a collaborative and inclusive work environment.