Validation Expert
$52,200–$96,900 year
On-sitePuurs, Flanders, Belgium
EXPIREDPuurs, Flanders, BelgiumOn-siteFull Time$52,200–$96,900 yearAssociates DegreeEnterprise
Full TimeAssociates DegreeEnterprise
Job Summary
Manage qualification status of validated process equipment and processes, including modification activities to comply with cGMP requirements. Prepare and verify process requalification protocols and reports with meticulous documentation, planning periodic requalification initiatives for manufacturing equipment, sterilisation, and aseptic process simulations. Ensure all activities adhere to current regulatory requirements by proactively managing deviations and maintaining audit/inspection readiness. Conduct risk assessments and collaborate with cross-functional teams to analyse and mitigate process risks.
Required Qualifications
- Scientific/Engineering Degree
- Previous experience within Quality/MS&T/Production department of a GMP manufacturing site
- Proactivity
- Flexibility
- Fluent in English
- Fluent in Dutch
Desired Qualifications
- Assembly Language (ASM)
- Change Controls
- Chemical Engineering
- Chemistry
- Continual Improvement Process
- Cost Reduction
- Data Analytics
- Electronic Components
- General Hse Knowledge (Inactive)
- Including Gdp (Inactive)
- Knowledge Of Capa (Inactive)
- Knowledge Of Gmp (Inactive)
- Lean Manufacturing
- Manufacturing Processes
- Manufacturing Production
- Pharmaceutics
- Process and Cleaning Validation (Inactive)
- Process Control
- Process Engineering
- Risk Management
- Root Cause Analysis (RCA)
- Six Sigma
- Standard Operating Procedure (SOP)
- Workforce Planning
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