We are looking for a committed expert for product development for a leading global player at the Ingelheim site. Join an innovative team and help shape the future of modern combination and medical products in an appreciative working environment. We look forward to getting to know you!
Here's what we offer
1. Attractive salary and long-term job security through group affiliation
2. Up to 30 days vacation per year
3. Contribution to company pension scheme after end of probationary period
4. Extensive social benefits, including Christmas and vacation bonuses
Your tasks
5. Responsibility for design verification: You will plan, coordinate and manage the verification processes for innovative medical devices throughout the entire development phase.
6. Compliance & Approval: You will ensure compliance with regulatory requirements and create all submission-relevant plans and reports for product approval.
7. Strategic development: You continuously optimize the implementation of regulatory requirements within the development processes.
8. Interface management: As a representative of the division in the device development team, you coordinate collaboration with engineering, quality, risk management and usability.
9. Operational implementation: You will carry out verification studies independently and take on important parts of design control.
Your profile
10. Successfully completed studies in a life sciences discipline (e.g. medical technology, biotechnology or pharmacy).
11. Several years of relevant experience in the development of medical or combination products.
12. Sound knowledge of the design control process and regulatory standards.
13. Practical experience in planning, conducting and documenting design verification studies.
14. Structured, precise approach and the ability to confidently manage complex projects in a regulated environment.