Job Description

Minimum of 6 years' experience primarily in medical device industry at a senior level
- Preferably finished goods
Must have worked in an FDA regulated environment:
- Having worked in a number of sites is preferable
- Experience working at a contract manufacturer is a plus
Have worked in contract roles before and be aware of what that entails (may forgo this in lieu of suitable experience at a contract manufacturer)
Must be capable of working in project environment:
- Focused on achieving deadlines while maintaining the required standard of work
- Capable to adapt and react to situations as they arise
- Flexible in both approach to work and hours on site
High level of experience with planning and executing all aspects of process validations
Pro-active, hands-on approach essential
Expected to lead by example and mentor the less experience members of the team
Must understand this is a remediation project and what that entails
High standard of English is essential:
- German is not a requirement
Remote work/working from home is not an option

Senior Validation Engineer