IPP works where medical devices become real: projects with real deadlines, regulatory responsibility, and customers who pay for outcomes — not slides. That’s why you won’t work “in the back office”. You’ll work close to the project and often in direct customer contact.
We think in structure, document cleanly, and communicate clearly — including when something is not sensible. At IPP, your work must hold up in reviews, audits, and in practice.
We use standards, templates, and tools consistently (e.g., Easy13485 / EasyExpert). AI tools like ChatGPT are a productivity lever — but they never replace responsibility. AI may propose, structure, and draft. You validate, decide, and stand behind the result.
Across all career levels, we expect:
Career at IPP is not about collecting titles. It is about growing responsibility: from owning your own tasks, to representing team results to the customer, to leading projects and customer relationships. We make expectations transparent so development becomes measurable — in feedback, in delivery, and in resuts.
We always keep one position open — independent of whether we hire immediately or not. The reason is simple: our workload depends on real projects. When new projects start, we hire fast. When capacity is already filled, we may pause hiring even if applications are strong.
What this means for you:
If you’re comfortable with that, applying still makes sense: we build our hiring decisions around delivery quality — not around fixed hiring cycles.
We work in real projects, with real deadlines and audit pressure. The fastest way to see if IPP fits you (and to stand out as an applicant) is to take our free Academy trainings.
How to use it: register, complete 1–2 short modules, and mention them in your application. It shows structured thinking, tool affinity, and the ability to deliver clean results.
Tip: If we are currently fully staffed, completing Academy modules still helps — we often reopen hiring when new projects start.
ipp Karriere
Karrierechance in der Medizintechnik Sie möchten als Regulatory Projekt Manager kontinuierlich Entwicklungsprojekte begleiten? IPP bietet spezialisierte Dienstleistungen für Hersteller von Medizinprodukten. Wir unterstützen in allen relevanten Bereichen der Erfüllung der Richtlinie 93/42/EWG oder MDR 2017/745. Mit uns gewinnen Hersteller Sicherheit
Pragmatic, evidence-first support for MDR and ISO 13485. We help you move from prototype to
market-ready device with clarity, speed, and audit confidence. (Pages in German)
