CQV Engineer - 195

Hybrid

Life Cycle

Quality & Compliance

Permanent Contract

Since 1993, ProductLife Group (PLG) has supported clients throughout the life sciences product lifecycle, combining local expertise with global reach and spanning more than 140 countries.

PLG is a life sciences consulting firm providing outsourced services in the areas of regulatory affairs, quality and compliance, vigilance and medical information. Our expertise extends to both established product monitoring and innovative therapies and diagnostics.

Why join PLG?

• International Company
• Multi-Projects on various types of activity in pharma, cosmetics, biotech and medical
• Large-scale projects with internationally renowned clients
• Upgrade skills
• A dynamic and motivated team

Benefits:

• Local management, dynamic and stimulating atmosphere
• PLG headquarters in the heart of La Défense (green spaces, gym, canteen, co-working rooms, gaming rooms)
• Social advantages (Mutual insurance, Restaurant Ticket Card, Bonus, Paid Leave, Transport coverage, Reimbursement of expenses linked to business travel, etc.)
• Partial teleworking possible

We are looking for a Qualification and Validation Consultant (CQV) W/M to join our teams.

Responsibilities

Manage periodic qualification and validation activities in the context of installation/modifications of equipment and processes. Your missions will be to:

• Supervise and execute qualification tests (FAT, SAT, QI, QO, QP, VP, VN, etc.), integrating the management of non-conformities;
• Write and update qualification/validation documents for the Quality Management System;
• Ensure monitoring of the qualification test schedule, as defined in the annual Validation Master Plan;
• Respond to and deal with non-conformities within your scope, by implementing quality, preventive or corrective actions.

Profile

• Engineer or bac+5 with a specialization in Quality;
• Significant experience in a similar Q&V position as part of a project for the construction of a new building and the installation of a filling line on a pharmaceutical site;
• Knowledge of regulatory requirements: ISO 13485, GMP, etc.;
• Good interpersonal skills, writing skills, organized, analytical mind, rigorous, autonomous, dynamic;