Design Quality Assurance Engineer (18 months contract)

Symetis SA — Ecublens VD
03.12.2019 | Employee | 100%


Symetis, a Boston Scientific Company, develops and produces innovative, minimally invasive heart valve replacement devices. The company’s product ACURATE neoand delivery systems, based on proprietary design and delivery technologies, are marketed and sold in key markets in Europe and in other markets, and are well positioned to target the constantly growing TAVI market.

Purpose and Passion:

At Symetis, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we’re solving some of the most important healthcare industry challenges. Together, we’re one global team committed to making a difference in people’s lives around the world. This is a place where you can find a career with meaningful purpose improving lives through your life’s work.


Design Quality Assurance Engineer


Role purpose:

In this position you fulfil the quality assurance responsibility of product development and related sustaining engineering activities. Furthermore you provide quality and technical input to the design reviews, project development, design change, recertification plans, risk management, design verification and validation protocols as well as reports for new development projects as well as design and process changes to existing product lines.


Tasks and Responsibilities:

  • Compilation of design verification and validation reports and design7quality documentation supporting product development and sustaining engineering project
  • Provide design quality support in the resolution of PIRs, complaints investigation, CAPAs, VIPs and regulatory requirement changes
  • Establish Design Control Matrix for new Products
  • Document Product Specifications
  • Define and Validate Test Methods
  • Create and maintain Risk Management Files incl. usability engineering plan

Your profile:

  • Graduate of Engineering (mechanical, biomechanical, physics, sciences or pharma)
  • Minimum of 3 years’ experience in Medical Device or Pharma industry
  • Excellent analytical and problem solving abilities
  • Experienced in analyzing and drawing conclusions for appropriate decisions from risk management activities and test data.
  • Fluent in French and English


Apply now:

If you want to make a difference and take on a new challenge, please let us know more about you and your possible start date by applying in English and clicking on the link below.

Employee, 100%


Symetis SA

Ch. de la Venoge 11

1024 Ecublens

No recruitment agencies please

Symetis SA

Ch. de la Vénoge 11Ecublens


Medical technology

Symetis SA

Ch. de la Vénoge 11Ecublens


Medical technology

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