In which organization will you work as a Quality Assurance - Engineering & Qualification Manager (M/F)?

We are currently looking, on behalf of one of our clients specialized in the pharmaceutical industry, for a Quality Assurance - Engineering & Qualification Manager (M/F), based in Occitanie, for a duration of 6 months.

Assignment Context

Within a pharmaceutical company operating in a regulated environment, the Quality Assurance - Engineering & Qualification Manager (M/F) will be involved in capital investment projects and upgrades of industrial facilities, including GMP infrastructures as well as production and analytical equipment.

In this context, he/she will lead Quality Assurance activities related to qualification and validation operations (including computerized systems), ensuring compliance with applicable regulatory requirements. He/she will also act as a key interface with cross-functional teams, particularly in deviation management and corrective action follow-up.

Quality Assurance - Engineering & Qualification Manager (M/F): What will be your missions and responsibilities?

Main Activities

• Lead Quality Assurance activities on industrial projects (new investments and facility upgrades)

• Oversee qualification and validation activities (including computerized systems) within a regulated environment

• Coordinate with technical and IT teams for deviation management, CAPA implementation, and Change Control follow-up

• Team management and activity coordination

What profile and skills are required for this position?

Education & Experience

• Minimum 5 years of experience in Quality Assurance within a pharmaceutical or regulated environment

• Up-to-date GMP training

• Experience in capital projects and/or industrial facility upgrades

• Experience in qualification/validation (equipment, utilities, computerized systems)

• Experience in deviation management, CAPA, and Change Control

• Professional level of English (preferred)

Technical Skills

• Strong knowledge of GMP regulations

• Expertise in CQV (Commissioning, Qualification & Validation) of equipment, utilities, and GMP infrastructures

• Knowledge of Computerized System Validation (CSV)

• Experience in technical and industrial project management

• Good understanding of GMP environments (cleanrooms, clean utilities, production and analytical equipment)

• Mastery of quality processes: deviations, CAPA, Change Control

Personal Skills

• Strong analytical and problem-solving skills

• Ability to communicate with cross-functional teams (technical, IT, production, quality)

• Ability to coordinate transversal activities

• Autonomy and proactive mindset

• Attention to detail and rigor

• Structured mindset with a strong focus on compliance

Interested in this opportunity? Apply now!

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

As part of our Quality, Health, Safety and Environment (QHSE) policy, we place strong emphasis on compliance with QHSE rules to ensure a safe working environment for our employees, while contributing positively to environmental protection.

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

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