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
Du möchtest Beratung auf das Nötigste reduzieren: Wie wäre es mit einem System, mit dem auch wir unser Team schnell arbeitsfähig machen? Eine abgestimmte Kombination aus Anleitung, Lernplattform, Templates, KI und Coaching.
Wir nennen das den Easy13485 Makerspace.
Du lieferst die Arbeit – wir liefern Struktur und steigen nur ein, wenn es kritisch wird. Wenn du eine einfache und sichere Lösung mit planbarer monatlicher Miete suchst, dann schau dir den Easy13485 Makerspace an: 5 klar strukturierte Bausteine – und in 10 Minuten weißt du, ob das eure Abkürzung ist. Follow Link >
Easy13485 delivers out-of-the-box speed with the flexibility to match each team’s unique setup.
Built to develop high potentials, the Academy turns training into a strategic growth tool.
Consultants are used strategically, not permanently.
Answers in seconds, so teams stay in flow and budgets stay lean.
Confidence on audit day – fewer findings, fewer costly loops.
