Berlin
Development Engineer – Medical Devices | Berlin
Your products treat cancer patients across 80+ countries. You own them from specification to production transfer — no hand-holding, no layers of approval. Just real engineering with direct impact.
Hands-on engineering with real ownership. Not coordination, not project management.
Why this role
▸ Profitable and stable company with multiple MDR and FDA approved products
▸ Real ownership – you drive your products end to end, visible from day one
▸ Three engineers plus technical lead — no matrix, no middlemen, short decision paths
▸ Brachytherapy and radiotherapy devices used in cancer treatment daily
Your responsibilities
▸ Own technical documentation – DHF, DMR, test plans – within MDR
▸ Drive the full lifecycle from specification through verification and validation
▸ Lead risk management activities in line with ISO 14971
▸ Communicate directly with suppliers on a technical level
▸ Coordinate testing with external laboratories
▸ Support design transfer into production including process qualification
Your profile
▸ Hands-on MDR CE experience – documentation ownership, not just exposure
▸ Full lifecycle experience from specification to validation
▸ Class IIa or higher devices, demonstrable on your own product
▸ 3 to 7 years in medical device development
▸ Team-oriented mindset
▸ Fluent English
▸ Based in Berlin or willing to relocate within 3 months
Nice to have
▸ ISO 14971 and IEC 60601 working knowledge
▸ Notified body audit experience (TÜV SÜD, DEKRA, BSI)
▸ Background in radiation therapy or active implants
▸ Process engineering background looking to broaden into development
Framework
▸ Location: Berlin, on-site
▸ Compensation: up to 80,000 € fixed + performance bonus
▸ Working language: English
▸ Start: as soon as possible
Interested?
Apply directly or reach out for a confidential conversation.