Do you work in quality assurance and are looking for a new challenge? Then we encourage you to apply, we look forward to hearing from you!
Working hours: 37.5 hours/week with flexible working hours
Up to 1 day/week remote work possible
Here's what we offer
1. Attractive salary and long-term job security through affiliation with a large corporation.
2. Up to 30 days of vacation per year
3. Company pension scheme contribution after the end of the probationary period
4. Extensive social benefits, including Christmas and holiday pay
5. Usually an open-ended employment contract
6. Good opportunities for acquisition with our business partners
7. Tailored professional development opportunities and free language courses
8. A wide range of employee benefits
Your tasks
9. Interface competence: You take over the central coordination and answering of product complaints, quality problems and official inquiries.
10. Communication hub: As the central point of contact, you will work closely with cross-functional teams (including Regulatory Affairs, Medical Service, Product Quality).
11. Expert network: They gather technical contributions from subject matter experts (SMEs) and consolidate them in a targeted manner.
12. Content & Quality: You formulate and finalize precise, high-quality written responses for internal and external stakeholders.
13. Deadline management: They strictly monitor deadlines and ensure timely delivery – especially in the case of official obligations.
14. Process control: You coordinate the internal testing and approval processes efficiently.
15. Compliance & Reporting: They carefully document all processes in the relevant quality systems, provide regular status updates, and proactively manage risks or delays.
Your profile
16. Education: Successfully completed Bachelor's or Master's degree in the life sciences field (e.g., biology, chemistry, pharmacy, medical technology, biotechnology) or a comparable qualification.
17. Professional experience: several years of sound professional experience in quality assurance (QA), regulatory affairs (RA) or complaint management within the pharmaceutical or medical technology industry.
18. Industry know-how: Familiarity with common regulatory requirements (e.g., ISO 13485, GMP, MDR, IVDR).
19. Communication and writing skills: Excellent written expression and the ability to formulate complex scientific and technical issues clearly, precisely and in a way that is appropriate for the target audience.
20. Working style: Strong project management and organizational skills, a high awareness of quality, and the ability to act confidently even under tight deadlines and priorities.
21. Global network: You will work in an international, highly collaborative environment with leading experts in the industry.
22. Deep insights: You will gain valuable, in-depth insights into strategic government communication and highly relevant quality processes.
23. Meaningful work with impact: A key role in which you directly contribute to patient safety, product quality and compliance with global guidelines.