Senior Research And Development Engineer

Barrington James; Zürich; Vor Ort; CHF 120.000 - 170.000; Vollzeit

Benefits dieser Stelle

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Zusammenfassung

Barrington James is seeking a Senior R&D Engineer for a medical-device organisation in Switzerland. You will own technical development from concept through verification, validation and transfer to manufacturing.

You will collaborate with Quality, Regulatory, Manufacturing and Clinical teams, shaping robust engineering solutions in a highly regulated environment.

Qualifikationen

• Experience in medical devices and regulated environments.
• Ability to translate user needs into robust designs.
• Strong understanding of design controls and lifecycle stages.

Aufgaben

• Lead engineering activities across the full lifecycle of medical-device products.
• Take technical ownership of complex development projects.
• Translate user needs into manufacturable engineering solutions.
• Lead design activities including specs, drawings, reviews, and docs.
• Develop and execute verification and validation strategies.
• Support risk management and ensure risk controls are in product designs.
• Mentor junior engineers and contribute to strategy.

Kenntnisse

R&D in medical devices

Design controls

Verification

Validation

Cross-functional teamwork

Mentoring

Ausbildung

Mechanical Engineering

Biomedical Engineering

Materials Engineering

Jobbeschreibung

We are supporting the growth of a medical-device organisation in Switzerland that is strengthening its R&D function and looking to connect with experienced Senior R&D Engineers.

This is an opportunity for an experienced medical-device engineer to take significant technical ownership across product development, from early-stage concept and design through verification, validation and transfer into manufacturing.

You will work closely with cross-functional teams including Quality, Regulatory, Manufacturing and Clinical/Technical functions, helping shape robust engineering solutions within a highly regulated environment.

Key Responsibilities

• Lead engineering activities across the full medical-device product-development lifecycle.
• Take technical ownership of complex product and component development projects.
• Translate user needs and product requirements into robust, manufacturable engineering solutions.
• Lead design activities including specifications, drawings, design reviews and technical documentation.
• Develop and execute design verification and validation strategies.
• Support design risk-management activities and ensure appropriate risk controls are incorporated into product designs.
• Lead technical investigations, root-cause analysis and design improvements.
• Provide technical input into design-transfer and manufacturing scale-up activities.
• Work closely with Quality and Regulatory teams to ensure compliance with applicable standards and regulatory requirements.
• Mentor and provide technical guidance to more junior engineers.
• Contribute to engineering strategy, technology development and continuous product improvement.
• Represent R&D in cross-functional project meetings and technical reviews.
• Support the resolution of complex technical and manufacturing challenges.

What We're Looking For

• Degree in Mechanical Engineering, Biomedical Engineering, Materials Engineering or a related technical discipline.
• Significant R&D/product-development experience within medical devices, MedTech, diagnostics or another highly regulated engineering environment.
• Strong understanding of design controls and the medical-device product-development lifecycle.
• Demonstrable experience taking products from concept through verification, validation and/or design transfer.
• Professional working proficiency in English; German