QMV Specialist
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 :
Job Description :
You will be responsible for implementing validation plans for processes, computerized applications, equipment qualification, and for overseeing their execution.
Activities:
- Implement the validation strategy for the site.
- Perform or oversee the validation and qualification of equipment, systems, processes, and methods (FAT, IQ/OQ, PQ, periodic PQ).
- Organize and coordinate validation and qualification activities for equipment with user departments.
- Contribute to defining qualification needs for equipment, utilities, IT systems, and analytical tools, and ensure their compliance with EU GMP standards by drafting protocols and reports.
- Draft quality documentation related to qualification and validation (SOPs, protocols, etc.).
- Apply regulatory requirements related to validation and metrology (internal or outsourced).
Reporting to the Quality Department, you will work in collaboration with Production, Quality Control, and the Technical Services of the site.
Your
profile :
Qualifications
• Education / Training
Master’s degree or Engineering degree in a scientific field.
- A minimum of 3 years of experience in the pharmaceutical industry is required.
• Technical Skills / Expertise
- Proficiency in English (spoken and written)
- Knowledge of production and control technical equipment
- Mastery of validation/qualification/metrology methods
• Behavioral Skills / Soft Skills
- Organized, rigorous, and autonomous
- Comfortable with versatility and working in human‑sized organizations
- Committed, team‑oriented, and eager to learn new things
