QA Specialist

Working in the Quality department, you will be responsible for ensuring product quality in compliance with GMP, cGMP and Public Health Code standards, in conjunction with other departments, and for releasing products manufactured on the Laval campus.

To do this,

You will monitor and deal with deviations, out-of-specification results and customer complaints, the associated investigations, and the implementation of corrective actions and improvement plans.
You manage certain quality processes and quality working groups (problem solving, quality projects).
You will participate in the company's quality processes and various quality projects:

- Documentation: procedures, instructions, etc.
- Validations
- GMP and cGMP compliance of premises
- Staff training
- External and internal audits
- Approval of suppliers and subcontractors.

**Your profile**:

- Level of education / training:
You are eligible for a position as interim or deputy pharmaceutical manager in charge of batch release. As such, you will hold a doctorate in pharmacy or veterinary medicine, or a Masters-level degree in chemistry, pharmaceutical chemistry and technology or biology.
- Technical skills/know-how:
You have at least initial experience in Quality Assurance, preferably in operational QA / batch release.

You are familiar with GMP and cGMP.

You are fluent in English.
- Behavioural skills / interpersonal skills:
You are rigorous, exemplary and autonomous.
You know how to communicate, adapt to your audience and instil a positive dynamic.

Your benefits at Ceva:
Fixed salary + variable,
Incentives, profit-sharing, attractive Company Savings Plan,
Health and provident scheme,
CSE benefits (holiday vouchers, gift vouchers, preferential prices (swimming pool, cinema, etc.)),
Teleworking, Time Savings Account,
Luncheon vouchers.