Cleaning Validation Specialist
Contracting – Antwerpen
Responsibilities
- Participate in functional meetings required to perform activities within scope.
- Perform periodic reviews of cleaning processes in three production departments (Oral Solid Dosages; Liquids, Ointments & Creams; Sterile) to ensure validated state.
- Coordinate and execute annual requalification studies (focus on 1 IPT, backup for another).
- Support cleaning projects (development & validation) for Partswashers, Clean In Place (CIP), and Manual methods.
- Coordinate activities with validation, production, and laboratories (appointments, LIMS requests, study execution, data evaluation).
- Support monitoring programs for potential cross-contamination through surface sampling.
- Provide urgent support for equipment cleaning issues (e.g., exceeding holding times).
- Handle deviations (administration, root cause analysis, CAPA).
- Perform change assessments or act as change owner.
- Contribute to closing audit gaps and observations.
Profile
- Bachelor in Chemistry, Biology, Biomedical Sciences or equivalent through experience.
- Strong analytical skills with attention to detail.
- Ability to work in a GMP-regulated environment.
- Good communication and coordination skills across multiple departments.
- Flexible to occasionally work in early/late shifts if required.
Our offer?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]