Quality Assurance Engineer

il y a 1 jour


Paris, Île-de-France Ceva Sante Animale Temps plein

Quality Assurance Engineer

The success of a company depends on the passionate people we partner with.

Together, let's share our talents.

As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.

We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.  

Indeed, Our "Together, Beyond Animal Health" vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.  

As part of our "Diversity, Equity and Inclusion" policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team. 

 

Your
missions :

Ceva Santé Animale is seeking a Quality Assurance Engineer (M/F) for its FILAVIE site.
This permanent position (CDI), starting on December 1st, 2025, is based in Sèvremoine (between Cholet and Nantes).

As part of the Quality Department, you will ensure product quality in compliance with GMP standards, in collaboration with other departments. You will also be responsible for the release of products manufactured on campus.

Your responsibilities:
- Ensure the monitoring of the quality assurance system from the receipt of raw materials to the distribution of finished products.
- Manage and process deviations, out-of-specification results, and customer complaints, including related investigations and the - - implementation of corrective actions and improvement plans.
- Contribute to the preparation of batch records and verify their compliance for internal release and submission to competent authorities.
- Lead certain quality processes and quality working groups (problem-solving, quality projects).
- Oversee Change Controls.
- Participate in the company's Quality processes and various quality-related projects, including:
Documentation: procedures, work instructions…
Validations
GMP and cGMP compliance of facilities
Staff training
Internal and external audits
Supplier and subcontractor approvals

This list is non-exhaustive.

Your
profile :

You hold a Bac+4/+5 degree (Engineering or Master's level) in Pharmaceutical Biology, Biotechnology, Industrial Bioproduction, or Health Products.

You have 6 months to 2 years of experience, along with a solid understanding of regulatory requirements in the pharmaceutical industry (GMP, cGMP, BPD…) and biotechnology processes.

You possess strong writing and interpersonal skills.

You are rigorous, well-organized, proactive, and a team player.

Ceva Santé Animale is committed to promoting employment for people with disabilities and considers all applications equally, including those from individuals with disabilities.



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