Gmp Compliance

Location:
**RIXENSART**
**#24233**

**GMP compliance**
**Our client**
Our client is looking for a profile in GMP Compliance to join its team. The QA Spare parts is part of the QA for Technical Services. They ensure the QA oversight of the spare parts warehouse.

**Your responsibilities**:

- Release spare parts to be used on GMP equipment throughout the company plant.
- Contact the spare parts' supplier in case of further investigation to allow release of the spare parts.
- Ensure on the floor presence and be the point of contact for the operational team.
- Participate to the strategy definition of the spare parts management and release.
- Process the backlog in release, investigations, and archives.
- Challenge the new spare parts creations.
- Review the modification proposed by the technical teams (MO).
- Quickly understand the regulatory requirements for the spare parts
- Use a risk-based approach for problem solving and prioritization of tasks
- Blow a quality and compliance mindset through the operational team
- Develop and continuously improve expertise linked to spare parts - expert on the field, technical and regulatory watch over, linked with global and corporate expertise functions

**Skills and knowledge requirements**:

- University degree (Biotechnology, Agronomy, Chemistry or Pharmacy)
- At least 5 years professional experience in pharmaceutical environment.
- Very good interpersonal relationship skills
- To be a good team player in order to success in each validation project.
- Fluent in French, good oral and written communication skills in English
- Problem solving and achievement oriented
- Knowledge of GMP Regulated environment
- Strong organizational skills

**Our offer**
Jefferson Wells offers you a permanent contract as a consultant with an attractive salary package and access to training in both technical and non-technical skills. We'll be your career partner every step of the way.