Clinical R&D Engineer

Clinical R&D Engineer

München Vollzeit 55350 - 67650 € / Jahr (geschätzt) Kein Homeoffice möglich
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Auf einen Blick

  • Aufgaben: Untersuche klinische Anforderungen und entwickle innovative Produkte für die Gesundheitsbranche.
  • Unternehmen: Quest Global, ein führendes Unternehmen im Bereich Ingenieurdienstleistungen mit über 25 Jahren Erfahrung.
  • Vorteile: Attraktives Gehalt, Gesundheitsleistungen und ein unterstützendes Arbeitsumfeld.
  • Weitere Informationen: Vielfältige und inklusive Unternehmenskultur, die kreative Ideen fördert.
  • Warum dieser Job: Gestalte die Zukunft der Medizintechnik und mache einen echten Unterschied im Leben der Menschen.
  • Qualifikationen: Abschluss in Biomedizin, Maschinenbau oder verwandten Bereichen; mindestens 6 Jahre Erfahrung.

Das prognostizierte Gehalt liegt zwischen 55350 - 67650 € pro Jahr.

Job Requirements At Quest Global, it’s not just what we do but how and why we do it that makes us different.

With over 25 years as an engineering services provider, we believe in the power of doing things differently to make the impossible possible.

Our people are driven by the desire to make the world a better place—to make a positive difference that contributes to a brighter future.

We bring together technologies and industries, alongside the contributions of diverse individuals who are empowered by an intentional workplace culture, to solve problems better and faster.

Key Responsibilities Investigates and defines clinical requirements for new product/feature development and facilitates the translation into new projects through clinical review and evaluation.

Works with field and medical personnel to define the benchmarks for evaluating the clinical performance of these products/features.

Simulates or tests aspects of new projects to evaluate prototypes and validate output as meeting customers’ intended use requirements; analyzes data collected from the field or from research studies.

Develops and directs preclinical evaluation protocols, data analysis, and reports Contributes to the evaluation and validation of a specific system or project as necessary to conduct feasibility studies, usability and human factors analyses, technology assessments, concept studies, benchmarking studies, or submission studies.

Provides input to the risk management file and Clinical Evaluation Reports in support of the product throughout its lifecycle.

Complies with U.

Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Performs other related duties and responsibilities, on occasion, as assigned.

We are known for our extraordinary people who make the impossible possible every day.

Questians are driven by hunger, humility, and aspiration.

We believe that our company culture is the key to our ability to make a true difference in every industry we reach.

Our teams regularly invest time and dedicated effort into internal culture work, ensuring that all voices are heard.

We wholeheartedly believe in the diversity of thought that comes with fostering a culture rooted in respect, where everyone belongs, is valued, and feels inspired to share their ideas.

We know embracing our unique differences makes us better, and that solving the worlds hardest engineering problems requires diverse ideas, perspectives, and backgrounds.

We shine the brightest when we tap into the many dimensions that thrive across over 21,000 difference-makers in our workplace.

Work Experience Qualifications BS Degree in biomedical, mechanical, electrical, biological or physical science.

Minimum of 6 years of relevant work of relevant work experience in medical product development and/or an equivalent combination of a graduate degree with relevant project experience.

Demonstrated ability to apply understanding of clinical application to issues in order to bring tasks to resolution within assigned projects.

Demonstrated ability to effectively integrate information from varied disciplines including Clinical Affairs, Engineering, Marketing and Regulatory Affairs.

Job Summary Job number: P-121401Date posted : 2026-08-03Profession: Med Tech and Healthcare Employment type: Full-Time

Experience: Qualifications BS Degree in biomedical, mechanical, electrical, biological or physical science.

Minimum of 6 years of relevant work of relevant work experience in medical product development and/or an equivalent combination of a graduate degree with relevant project experience.

Demonstrated ability to apply understanding of clinical application to issues in order to bring tasks to resolution within assigned projects.

Demonstrated ability to effectively integrate information from varied disciplines including Clinical Affairs, Engineering, Marketing and Regulatory Affairs.

Clinical R&D Engineer Arbeitgeber: Quest Global Services

Quest Global ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern die Möglichkeit bietet, an bedeutenden Projekten in der Energiebranche zu arbeiten. Mit einem starken Fokus auf Teamarbeit und Innovation fördert das Unternehmen eine Kultur des kontinuierlichen Lernens und der persönlichen Entwicklung, während es gleichzeitig flexible Arbeitsbedingungen und umfangreiche Reisegelegenheiten bietet. Die Position des FACTS Commissioning Engineers ermöglicht es Ihnen, Ihre technischen Fähigkeiten in einem dynamischen Umfeld einzusetzen und dabei zur Lösung komplexer Herausforderungen beizutragen.

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Kontaktdaten:

Quest Global Services Recruiting-Team

Wir glauben, dass du diese Fähigkeiten brauchst, um Clinical R&D Engineer mit Bravour zu bestehen

Klinische Anforderungsanalyse
Produktentwicklung
Datenanalyse
Prototypenvalidierung
Risikomanagement
Regulatorische Anforderungen (FDA)
Kommunikationsfähigkeiten