This role ensures all computerized systems meet validation, compliance, and regulatory requirements within a pharmaceutical environment
Job Summary
This role ensures all computerized systems meet validation, compliance, and regulatory requirements within a pharmaceutical environment.
The position offers a competitive salary ranging from €57,800 to €79,420 along with comprehensive benefits including private medical insurance and retirement contributions.
Candidates will collaborate cross-functionally on technology transfers while maintaining the highest standards of quality, safety, and data integrity.
Matching Summary
This role ensures all computerized systems meet validation, compliance, and regulatory requirements within a pharmaceutical environment.
Salary
Base: €57,800.00 - €79,420.00; Bonus: Performance-based bonuses included; Benefits: Retirement plan, private medical insurance, dental, life insurance, and flexible options
Skills & Requirements
Must-have
Minimum 3 years CSV experience in pharma
Bachelor's degree in Engineering or Science
Expertise in URS, DQ, FAT/SAT, IQ/OQ protocols
Knowledge of 21 CFR Part 11 and data integrity
Experience with CAPEX projects and technology transfer
Nice-to-have
Familiarity with Kneat Paperless Validation tool
Experience in API or Drug Product manufacturing
Strong technical writing and communication skills
Ability to drive continuous improvement initiatives
Self-motivated with willingness to contribute beyond core duties
Key Requirements
Bachelor's degree in Engineering or Science
3+ years CSV experience in pharmaceutical industry