Responsibilities
- Carry out validation procedures for equipment and systems used in pharmaceutical settings, with emphasis on storage areas, cold storage units, and non-cleanroom environments
- Assist in computer system validation efforts for software used in production and laboratory operations, including embedded equipment software
- Conduct validation of spreadsheets to maintain data accuracy and adherence to regulatory standards
- Record validation processes and manage documentation in compliance with GxP guidelines
- Work with multidisciplinary teams to detect and address validation challenges
- Contribute to the creation of validation plans, protocols, and summary reports
Work Arrangement
Remote with daily travel to Leuven required
