Product Quality Review Technician (M/F)

LE CABINET RH - LCRHYonneEURESpublished 10/02/2026
Machine translation — original language: French.Show original

Le Cabinet RH - LCRH: We are a recruitment firm connecting candidates and companies for permanent positions (CDI) directly with our clients.

Our firm is supporting a player in the pharmaceutical sector in the recruitment of a Quality Technician specialized in Product Quality Review.

At the heart of the site's activities, you will ensure the quality and compliance of product files, in connection with regulatory requirements, internal procedures, and customer expectations.

Your missions:

You will be responsible for drafting Product Quality Reviews (PQR), in compliance with GMP and current procedures. To prepare these documents, you will collect the necessary information from the production, quality control, and quality assurance teams, then analyze data relating to manufacturing and the controls performed.

You are the guarantor of the consistency and quality of the elements integrated into the PQRs, as well as compliance with agreed deadlines. You will monitor the progress of files and coordinate exchanges with internal stakeholders to gather missing data within the deadlines.

In connection with the Sales Administration (ADV) department, you will participate in the monitoring of associated quotes and invoicing. You will also be the point of contact for customers regarding their requests concerning PQRs and contribute to providing clear, reliable, and documented answers, including in written English.

Finally, you will take part in the site's Quality projects and may contribute to the improvement of practices and processes related to the preparation and monitoring of quality reviews.

You hold a Bac +2/3 degree in quality, chemistry, biology, pharmacy, or an equivalent field - BTS, DUT, or professional license.

You have proven experience in drafting PQRs in a pharmaceutical or CDMO environment, which has allowed you to become familiar with applicable requirements and exchanges between the different teams of a site.

You master Good Manufacturing Practices (GMP) and know how to exploit data from production and quality control to draft structured and reliable documents. Knowledge of a quality management system, such as M3 or Ennov, is an asset.

You possess excellent writing skills, master office tools, particularly Word and Excel, and are comfortable with technical written English, which is essential for handling requests from international customers.