Quality Assurance Pharmacist

#JobOffer #QP #Pharmacist #Industry

As Deputy Qualified Person, you will be responsible for the pharmaceutical establishment and guarantee the quality, operational and regulatory processes in compliance with the applicable standards.

The Company

CEVIDRA is a family-owned pharmaceutical company specializing in the marketing of high added value drugs and which wants to make innovative therapies accessible to thousands of French patients suffering from rare diseases. Cevidra offers unique and comprehensive support in BtoB and covers activities related to the operation, manufacturing, storage and distribution of products. Since its creation in 2007, CEVIDRA has reached its highest turnover with more than 13 M€ and has experienced strong acceleration in recent years.

The Job Description

Your missions mainly break down as follows:

  • Maintain the site’s quality system and be responsible for pharmaceutical operations
  • Assess the criticality of deviations, customer complaints and monitor corrective and preventive actions (CAPA);
  • Ensure regulatory control of changes within the company; o Propose and implement quality monitoring and improvement tools and lead the management review.
  • Ensure the review of drug packaging and pharmaceutical release files;
  • Coordinate and supervise product distribution activities for the French territory.
  • Supervise the site’s regulatory activities o Contribute to the quality support of the site’s strategic development projects (distribution of medicines in Europe);
  • Coordinate Price/Reimbursement & Advertising files for Cevidra products, in collaboration with our experts on these files;
  • Act in as Local Pharmacovigilance Manager (RPV): setting up and monitoring pharmacovigilance processes;
  • Maintain the Medical Information process: feedback from the field, answers to questions from professionals;
  • Guarantee the processes related to the launch of new products and the monitoring of marketing from a regulatory (AMM & variations) and operational point of view.
  • This list is not exhaustive and may change depending on your skills, the objectives of the company and the problems encountered.


You are rigorous and autonomous. You have good interpersonal and organizational skills and a good level of English. You are a Pharmacist eligible for the functions of PRI section B/C of a pharmaceutical operator & manufacturer laboratory.

You have several years of experience in the industry pharmaceutical company in similar functions and demonstrate solid skills in the regulation of the activities of an operator/manufacturer site.

So don’t hesitate to apply.

Other information

Occasional trips to France and Europe to industrial partners are to be expected.

CDI – based in Grasse with possibility of 1 day teleworking/week Position to be filled Q4 2022 /Q1 2023

Remuneration according to experience (> 70k€)

Cevidra is a company of the Pharmaceuticals group DESTAING PARTICPATIONS

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