Job Description
Key Responsibilities
- Ensure that clinical batches are manufactured in compliance with GMP standards and Quality Agreements
- Act as a QA PIP at the CMO, providinghands‑on oversight by:
- Witnessing critical sterility assurance activities (e.g. sterile setup, filling)
- Performing GEMBA walks when required to ensure process compliance
- Escalate critical quality issues and support impact assessments in collaboration with the CMO
- Oversee Drug Product manufacturing processes, including:
- Drug Substance thawing
- Compounding
- Filling
- Freeze‑drying
- Capping
- Visual inspection
- Storage
- Support the investigation, follow‑up, and closure of deviations, inclu...
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Submit ApplicationJob Details
- Location Wavre, Wallonia
- Job Type Temporary
- Category Business Operations Specialists
- Posted Date June 11, 2026
- Application Deadline July 21, 2026