Regulatory affairs is a matter of trust — and trust is built through people.
Careers at regular services
regular services supports manufacturers of medical devices and in vitro diagnostics throughout the entire regulatory process — from the initial assessment to ongoing market support. What sets us apart is not consulting from the drawing board, but practical implementation alongside our clients.
For this, we are looking for people who want to engage deeply on a technical level and who see client contact not as an obligation, but as the core of their work.
A short cover letter and your CV are enough to get started. We’ll clarify everything else in a conversation.
What awaits you with us
With us, you work independently and with real scope to shape things — not as a cog in a large corporation, but as part of a team in which your work becomes visible. You accompany real approval projects, communicate directly with Notified Bodies and authorities, and pass on your knowledge in training courses, among other things together with our cooperation partner, the TÜV Rheinland Akademie.
We value the compatibility of work and family life: permanent employment, full-time or part-time, with the option of working from home.
Who we are looking for
We would particularly welcome applicants in two focus areas:
Regulatory Affairs (RA):
You develop regulatory strategies, prepare and edit Technical Documentation for CE and international markets, and classify medical devices according to their Intended Purpose. Writing approval-relevant documents comes easily to you.
Quality Management (QM):
You support manufacturers in setting up and optimising their QM systems, conduct internal audits and further develop our QM reference system. Precise wording in a QM context is your strength.
In both roles, you bring:
a completed degree in medical engineering, a background in the natural sciences or a comparable qualification, professional experience in QM or RA for medical devices, an enjoyment of working with clients, and business-fluent German and English skills. Experience with country-specific regulatory requirements is a plus.
Regulatory affairs is broad – and our team grows with the topics. If you would like to contribute your expertise to us but don’t fully fit either of the two profiles, we would still be glad to hear from you.