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 Pharmaceutical Quality Assurance Consultant W/M to join our teams.

Group 10

You guarantee compliance with GMPs and compliance with regulations and quality procedures in force during your missions to our clients.
You will be required to work on various missions in Quality Assurance:
QA System

  • Management of the quality management system (writing/updating) of procedures, instructions
  • Supplier management (writing/updating specifications)
  • Training management (implementation of training module, animation of the module)
  • Plan and coordinate internal and external audit schedules
  • Be the reference for the quality management system with the competent authorities, notified bodies and certifiers.
    Operational QA
  • Management of Quality events (deviations / CAPA, Change Control, complaints, etc.)
  • Production support (optimization of processes to comply with GMP)
  • Lead the various quality system processes in place in the company and validate their compliance.

Group 13

  • Pharmacist writable section B ideally
  • BAC+5 Engineer or Scientist in the field of health , chemistry , biochemistry or processes
  • Significant experience in Quality Assurance
  • Good quality relational, ease editorial, organized, analytical mind, rigorous, autonomous, dynamic
  • Fluent English required
  • French mandatory

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