Which organization will you join as a CQV Technician / Engineer (M/F)?

We are looking, on behalf of one of our clients-a major player in the pharmaceutical industry-for a CQV Technician / Engineer (M/F). The position will be based in the Auvergne-Rhône-Alpes region for a duration of 4 to 6 months, renewable.

Assignment context

Within one of our pharmaceutical clients operating in a highly regulated environment, the CQV Technician / Engineer (M/F) will be involved in a project for the qualification of laboratory equipment and associated computerized systems.

The objective is to ensure regulatory compliance (GMP) and equipment reliability through the execution of qualification activities (IQ, OQ, PQ).

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

Main mission

In collaboration with Quality, Validation, Production teams, and suppliers, you will be responsible for qualifying laboratory equipment and associated systems in compliance with regulatory requirements and site quality standards.

Main activities

Perform risk/criticality assessments and contribute to the qualification strategy
Draft qualification protocols (IQ, OQ, PQ)
Execute qualification tests on equipment (laboratory and associated utilities)
Analyze results and manage deviations (deviations, CAPA)
Write qualification reports
Coordinate with suppliers and internal teams (QC, QA, IT, maintenance)
Participate in FAT/SAT when required
Qualify computerized systems associated with equipment (CSV)
Update quality documentation (SOPs, traceability matrices, etc.)
Contribute to regulatory compliance and audit/inspection readiness

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

Education & experience

Degree ranging from Associate's to Master's (pharmaceutical sciences, biotechnology, quality, engineering, or equivalent)
Minimum 2 to 5 years of experience in CQV / validation within the pharmaceutical industry
Experience in laboratory equipment qualification (QC)
Knowledge of GMP environments (mandatory)
Experience in CSV (Computer System Validation) is a plus
Professional English (preferred)

Technical skills

Strong knowledge of qualification activities (IQ, OQ, PQ)
Familiarity with laboratory equipment (HPLC, chambers/incubators, autoclaves, etc.)
Understanding of computerized systems associated with equipment
Knowledge of GMP / GxP standards
Proficiency with quality and documentation tools (deviations, CAPA, change control)
Ability to work on multiple equipment/projects simultaneously

Personal qualities

Rigorous and detail-oriented
Strong analytical and synthesis skills
Autonomous and proactive
Good interpersonal skills and ability to work cross-functionally
Ability to manage priorities in a demanding environment

Interested in this position? Send me your application!

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 great importance on compliance with QHSE rules to ensure a safe working environment for our employees, with the ambition of making a positive contribution to the environment.

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 required to follow HSE procedures and best practices while contributing to the continuous improvement of our processes.