Job Description

In what environment will you work as a CQV Engineer (M/F)?

We are currently looking, on behalf of one of our clients, a major player in the pharmaceutical industry, for a CQV Engineer (Commissioning, Qualification & Validation) (M/F) based in Normandy for 11 months.

Mission Context

Within a pharmaceutical manufacturing site, the CQV Engineer (M/F) is involved in projects related to the commissioning, qualification, and validation of critical equipment and installations.

In compliance with GMP requirements and international quality standards, you will play a key role in drafting, planning, and executing CQV activities, ensuring regulatory compliance, full documentation traceability, and process robustness throughout the equipment lifecycle.

CQV Engineer (M/F): What will your missions and responsibilities be?

Main Mission

In collaboration with Technical, Production, and Quality Assurance teams, you will ensure the proper execution of Commissioning, Qualification & Validation (CQV) activities for pharmaceutical installations and critical equipment, in full compliance with regulatory requirements and Good Manufacturing Practices.

Main Activities

• Drafting, planning, and executing qualification and validation protocols and reports (IQ/OQ/PQ, FAT/SAT, automated testing, etc.)
• Participating in equipment commissioning activities
• Ensuring documentation consistency and traceability throughout the equipment lifecycle
• Working cross-functionally with Technical, Production, and Quality Assurance teams
• Managing deviations, conducting Root Cause Analyses (RCA), and proposing corrective and preventive actions
• Contributing to validation strategy development and continuous improvement initiatives
• Actively supporting the optimization of CQV processes at site level

What profile and skills are required for this CQV Engineer (M/F) position?

Education & Experience

• Engineering degree or equivalent in engineering, pharmacy, or a scientific discipline
• 2 to 5 years of successful experience in CQV projects within the pharmaceutical industry
• Practical knowledge of GMP requirements and quality standards (ISO, GxP, etc.)
• Experience in a pharmaceutical manufacturing environment
• Professional proficiency in written and spoken French (technical documentation and team interactions)
• Good level of English is considered an asset

Technical Skills

• Strong knowledge of Commissioning, Qualification & Validation activities (IQ/OQ/PQ, FAT/SAT)
• Solid understanding of pharmaceutical regulatory requirements (GMP, data integrity, traceability)
• Technical documentation writing skills
• Risk assessment and deviation management capabilities
• Good understanding of pharmaceutical equipment and industrial processes

Personal Skills

• Strong attention to detail and quality-oriented mindset
• Analytical thinking and problem-solving skills
• Ability to work autonomously while being a collaborative team player
• Strong organizational skills
• Sense of responsibility and ownership
• Continuous improvement mindset

Interested in this position? Send us your application!

EP2C Energy is committed to diversity and inclusion. We encourage applications from candidates recognized as disabled workers.

As part of our Quality, Health, Safety, and Environment (QHSE) policy, we place the highest importance on compliance with QHSE rules to ensure a safe working environment for our employees, with the ambition of contributing positively to the environment.

Our company is committed to continuous improvement through its Quality Management System (QMS) and Health, Safety and Environment Management System (HSEMS).

By joining our teams, you will be required to follow HSE procedures and best practices while contributing to the continuous improvement of our processes.