
Validation Process Engineer – Life Sciences
Minor Hotels Europe and Americas
full-time
Posted on:
Location Type: Hybrid
Location: Diegem • Belgium
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About the role
- be a key member of the Process Validation team
- focusing on aseptic production validation activities
- determining and improving Aseptic Process Simulation (APS) strategies
- writing comprehensive APS protocols and reports that meet Good Documentation Practice (GDP) standards
- preparing materials for APS runs and ensuring all necessary components are available
- analyzing validation results and providing recommendations for process improvements
- training operational teams on aseptic techniques and validation procedures
- collaborating with cross-functional teams to ensure validation activities align with production schedules
- contributing to continuous improvement initiatives within the validation department
Requirements
- Bachelor's or Master's degree in Pharmaceutical Sciences, Bioengineering, Chemical Engineering, or related field
- 3-7 years of experience in process validation, preferably in aseptic pharmaceutical environments
- Expertise in media-fill validation and aseptic techniques
- Strong understanding of GMP regulations and their application in pharmaceutical manufacturing
- Good project coordination skills
- Good communication skills, both written and verbal, with ability to write clear and compliant validation documentation
Benefits
- flexibility in more than one way
- hybrid way of working
- flex abroad program offering up to 45 days abroad
- career growth programs
- employee led networks dedicated to advance diversity, equity and inclusion
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
aseptic production validationAseptic Process Simulation (APS)media-fill validationGood Documentation Practice (GDP)process validationvalidation documentationGMP regulations
Soft Skills
project coordinationcommunication skillstrainingcollaborationanalytical skills