Industrial Development Project Manager

Ceva Santé Animale • 24 days ago

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Salary

≈ $52k – $86k per year (Estimated)

Location

In office (Libourne)

Confirmed on the employer's own hiring board on Oct 25, 2026. First seen by Alion on Jun 2, 2026. Ceva Santé Animale scores A on the Alion truth index.

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Ceva Santé Animale

Ceva Santé Animale is a French animal health company headquartered in Libourne that develops, manufactures and sells veterinary medicines, vaccines and welfare products for livestock, poultry and companion animals. Founded in 1999 through a management buyout of the animal health business of Sanofi, it has grown into one of the largest animal health companies in the world, with research centres, production plants and subsidiaries across Europe, the Americas, Asia and Africa. It hires veterinary service managers, research and development project managers, manufacturing leaders, regulatory and quality staff and sales teams.

ceva.com • HQ: Libourne, France • Vaccines • Veterinary Medicine • 5000+ employees • Est. 1999

Tech stack of Ceva Santé Animale

Backed by ARCHIMED, Mérieux Equity Partners

Context As part of the development of its activities, the Global Industrial Development department is recruiting an Industrial Development Project Manager (M/F). You will play a central role in the industrial transfer of strategic projects, particularly for new products and technology transfers, ensuring a smooth transition between development and commercial production phases. Missions Industrialization project management:

Define and lead the industrialization strategy.
Contribute to process selection (Quality by Design approach).
Coordinate R D and industrial teams.
Write protocols and reports for process optimization and validation.
Monitor batch manufacturing in compliance with GMP and analyze results.
Ensure product compliance, cost and timeline adherence, and integration of technical and regulatory updates. Technical support to the production site:
Participate in supplier and process change validations.
Actively contribute to troubleshooting related to production processes.
Supervise galenic/industrial trials and risk analyses (FMEA). Department activities:
Contribute to drafting procedures, audits, inspections, and documentation follow-up.

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