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

– 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.

Group 10

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

  • Write IQ, QO, QP, VP, VN… protocols;
  • 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.

Group 13

  • 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 13 485, GMP, etc;
  • Good interpersonal skills, writing skills, organized, analytical mind, rigorous, autonomous, dynamic;
  • Fluent English required;
  • French mandatory.

CQV Engineer - 195