For the Production Department of our Tübingen location, we are looking for an
Validation Engineer (m/f/d)
Your Responsibilities
- Serve as a point of contact for cross-departmental technical matters and help resolve validation issues
- Monitor and maintain the master validation plan in the production environment
- Update, develop and train process validation in accordance with the applicable standard and GMP specifications (ISO 13485; 21 CFR 820)
- Perform process validation, revalidation and trend analyses as required
- Review and approve validation plans in accordance with internal validation specifications for manufacturing processes, test methods, equipment and utilities
- Create, update, train and review the application of work instructions and document templates
Your Skills
- Degree in medical technology, engineering with a focus on mechanical engineering, mechatronics, or a comparable study programme
- Several years of professional experience in product and process validation
- Basic technical understanding of devices and systems
- Experience in using Minitab statistical software is an advantage
- Conscientious, independent and structured way of working
- Good communication skills and assertiveness
- Good command of English
Benefits:
- Flexible working hours
- Induction program and on-demand training
- Friendly work environment
- Occupational health and safety management
- Occupational pension plan
- A secure workplace in a modern company
Are you interested?
If so, we look forward to receiving your application, including your salary expectations and the earliest possible starting date. Please apply via mail to career@erbe-med.com.