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Associate Engineer; m​/f​/d Development Disposables

in 80331, München, Bayern, Deutschland
Unternehmen: Getinge
Vollzeit position
Verfasst am 2026-03-06
Berufliche Spezialisierung:
  • Ingenieur
    Produktingenieur, Biomedizinischer Techniker, Ingenieur für Medizinische Geräte
Gehalts-/Lohnspanne oder Branchenbenchmark: 100000 - 125000 EUR pro Jahr EUR 100000.00 125000.00 YEAR
Stellenbeschreibung
Stellenbezeichnung: (Associate) Engineer (m/f/d) Development Disposables

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life‑saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

We are currently looking for a self‑driven and open‑minded (Associate) Engineer (m/f/d) Development Disposables to join our team in the research and development (R&D) department in Feldkirchen, Germany, part of the product area Critical Care  team is responsible for the development and product care of sterile single‑use sensor systems for the PiCCO, ProAQT and NAVA Technology.

We at Getinge believe in self‑organised and cross‑functional teams, adopting to lean and agile methods in product development and project management. Our vision is to successfully realise customer value in medical technology in a fast changing and complex environment.

We closely collaborate with other international Getinge sites in Sweden, Germany and the US within our business area Acute Care Therapies. Also, daily cooperation with our contract manufacturing partners is key.

As an (Associate) Engineer (m/f/d) Development Disposables
at Getinge we would like you to manage and support product development and product care initiatives. You will also have opportunities to grow into an expert role to further optimise our products with focus on user‑centered design, sustainability and sterilisability.

Tasks & Responsibilities
  • Manages and/or supports the design, development, and implementation of new medical device sensor systems, including sterile disposable/consumable sensors, reusable mechatronic components, and connection solutions, applied in advanced hemodynamic monitoring and ventilation
  • Drives and supports product care projects (design changes) aimed at improving and optimizing existing devices and components
  • Utilises lean, agile, and visual methodologies in product development and project management to collaborate effectively in a self‑organising team
  • Serves as an expert within the team in one or more areas related to the design of single‑use medical sensor systems (e.g., biocompatibility, CAD design, sterilisability)
  • Investigates and resolves technical issues related to product performance, production processes, and equipment
  • Coordinates design transfer to suppliers until serial production release, including the development of manufacturing processes and equipment
  • Works closely with internal departments (Quality, Regulatory, Product Management, Operations) and external partners such as test laboratories, service providers, and suppliers
  • Prepares technical documentation (DHF/DMR) for product designs, risk analyses, product specifications, etc., in accordance with established product development procedures and relevant regulations (MDR/21 CFR 820)
  • Evaluates and implements requirements from applicable standards
  • Continuously develops engineering skills through formal training provided by GETINGE, as well as coaching and mentoring from leaders and teammates
Desired Profile
  • University degree (Bachelor, Master, Diplom) in Medical Engineering, Biomedical Engineering, Plastics Engineering, Mechatronic Engineering, or a closely related discipline
  • First relevant hands‑on engineering experience in the medical device industry is desirable. Motivated graduates are also welcome
  • Broad understanding of the medical device development process and its interfaces with internal company support functions
  • Experience with lean and agile frameworks (e.g., Scrum, Kanban, Design Sprint, Design Thinking) and self‑organising teams is desirable
  • General knowledge of major manufacturing and assembly techniques used in single‑ and multi‑use medical devices
  • Willingness to take on and grow into an expert role. Existing competence in sterilization, biocompatibility, user‑centered design, sustainable design, or other relevant areas is a plus
  • Experience with CAD tools (e.g., Solid Works) is beneficial
  • Analytical mindset and well‑organised working style
  • Fluent in written and…
Stellen-Anforderungen
10+ Jahre Berufserfahrung
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