Pharmaceutical Validation Consultant (CQV) – Life Sciences Specialist (M/F/O)

As a Pharmaceutical Validation Consultant (CQV) – Life Sciences Specialist, you will coordinate and oversee the qualification of critical systems essential for pharmaceutical production. Your role will ensure compliance and operational excellence by supporting and guiding local teams throughout the validation process.

• Coordination of Commissioning, Qualification, and Validation:

Coordinate the development and execution of qualification protocols (IQ/OQ/PQ) for utilities, including Clean and Black Utility systems. Oversee commissioning and qualification activities for electrical and HVAC systems, ensuring adherence to the highest standards of quality and compliance.

• Technology Transfer and Support to Validation Teams:

Manage technology transfers, ensuring robust procedures are established for seamless transitions. Provide guidance and technical support to local validation teams to maintain consistency and efficiency across processes.

• Process Validation and Compliance:

Ensure validation procedures are implemented and documented effectively for audit readiness. Oversee compliance with GMP regulations and specific pharmaceutical industry standards across all validation activities.

• Workload and Deadline Management:

Manage project demands efficiently in a high-volume environment. Reassign tasks and responsibilities within teams to optimize resources and maintain project progress on schedule.

Company details

Akkodis offers broad industry experience, and strong know-how in key technology sectors such as mobility, software & technology services, robotics, testing, simulations, data security, AI & data analytics. The combined IT and engineering expertise brings a unique end-to-end solution offering, with four service lines – Consulting, Solutions, Talents and Academy – to support clients in rethinking their product development and business processes, improve productivity, minimize time to market and shape a smarter and more sustainable tomorrow. Akkodis is part of the Adecco Group.

Candidate’s Profile

• Education: Degree in engineering (mechanical, electrical, biochemistry, or equivalent).
• Experience: Minimum of 8 to 10 years in a CQV role, with a strong background in black & clean utilities and in the qualification/validation of electrical and HVAC systems. Experience within large pharmaceutical companies is highly valued.
• Technical Skills: Advanced expertise in commissioning, qualification, and validation processes, with a solid understanding of GMP practices.
• Languages: Proficiency in English is required; knowledge of French or German is a plus.