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R&D Sustaining Engineer (m​/f​/d

in 14513, Teltow, Brandenburg, Deutschland
Unternehmen: OLYMPUS EUROPA SE & CO. KG
Vollzeit position
Verfasst am 2026-08-21
Berufliche Spezialisierung:
  • Ingenieur
    Ingenieur für Medizinische Geräte, Fertigungsingenieur, Biomedizinischer Techniker, Elektrotechnik-Ingenieur
Gehalts-/Lohnspanne oder Branchenbenchmark: 65000 - 95000 EUR pro Jahr EUR 65000.00 95000.00 YEAR
Stellenbeschreibung
Stellenbezeichnung: R&D Sustaining Engineer (m/f/d)
Location: Teltow

R&D Sustaining Engineer (m/f/d)
Olympus Winter & Ibe GmbH (OWI)
Chief Technology Officer

As a high-tech specialist within the Olympus Corporation, Olympus Surgical Technologies Europe is the development and manufacturing center for rigid endoscopy, bipolar high-frequency surgery and reprocessing. With a total workforce of 2,600 employees at nine locations in EMEA and its headquarters in Hamburg, the company stands for exceptional performance in medical diagnostics and therapy, and offers a full range of the most modern endoscopic applications, from single products to procedure-oriented systems solutions.

Your Responsibilities
  • Provide support to products post launch, coordinating design and manufacturing changes and improvements to meet defined specifications (esp. device and manufacturing requirements) as part of life cycle management (changes, QIS, CAPA etc.) in cooperation with other specialist departments, taking into account medical application requirements and economic requirements. This applies to both in-house and purchased products and assemblies.
  • Provide support to products post launch, coordinating design and manufacturing changes and improvements to meet defined specifications (esp. device and manufacturing requirements) as part of life cycle management (changes, QIS, CAPA etc.) in cooperation with other specialist departments, taking into account medical application requirements and economic requirements. This applies to both in-house and purchased products and assemblies.
  • The particular focus is on the electrical design of the system and its components, taking into account the various subsystems.
  • Maintain a strong and current understanding of relevant new product development and manufacturing technologies and their application to medical device design to meet or exceed customer, company and project needs
  • Evaluation and documentation of the feasibility, reliability and risk of concepts and / or prototypes through engineering testing and analysis in order to demonstrate that the product performance, manufacturability, safety and cost are consistent with the customer, regulatory and production requirements
  • Generate, modify and review design history file documentation in compliance with relevant regulatory requirements e.g. Quality System Regulations (QSR), Good Manufacturing Practice (GMP), International Standards Organisation (ISO) and in accordance with company development standards (e.g. PDD, TDP) throughout the product life cycle to ensure the design is fully documented
  • Progress vendor activities in agreement with global sourcing relative to communication of specifications, development schedules and tracking in order to obtain components, supplies or equipment to support prototype or product procurement and assembly
  • Deliver manufacturable designs acceptable to operations by applying design for manufacture principles, implement and communicate feedback from manufacturing engineers, external suppliers and other sources to the R&D engineer
Your qualification
  • Bachelor’s or Master’s degree in Electrical engineering or equivalent professional education
  • 4+ years of professional experience
  • Confident handling of analogue and digital measurement technology (oscilloscope, analysers)
  • Experience with the creation of circuit diagrams and circuit board design
  • Knowledge of the process-orientated development of medical products is desirable
  • Independent and goal-orientated way of working as well as the ability to work in a team and a pioneering spirit
  • Experience in the area of standardization and certification of medical devices (IEC 60601-1, EMC, ISO, EN).
  • Experience in sustaining regulated devices under Design Control (21 CFR 820), ISO
    13485, ISO
    14791, MDR and knowledge of applicable regulations
  • Good or better written and spoken English skills
  • Strong collaboration skills with internal and external partners
  • Ability to work effectively in a multicultural environment
Your benefits
  • 30 days of annual leave
  • Up to 60% mobile work possible + flexible work time model with overtime compensation
  • Holiday and Christmas bonuses
  • Corporate benefits discounts for employees
  • Comprehensive company pension scheme and capital-forming benefits
  • C…
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