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Equipment Engineer (Manufacturing) Job

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Date: Jun 19, 2019

Location: Ecublens, VD, CH

Company: Boston Scientific


Symetis SA, 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 Boston, 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.



Apply Engineering to improve Product Quality, Customer Service and reduce Costs by optimizing current Manufacturing Equipment or managing new Equipment Development Projects.



  • Demonstrates a commitment to patient safety and product quality.
  • Observes and complies with all safety rules and regulations. This includes QSR and ISO Standards.
  • Provide technical support on maintenance and equipment issues.
  • Performs Equipment assessment and identifies subsequent Improvement activity
  • Demonstrate basic technical knowledge to innovate, develop and/or support processes, procedures, tooling and/or automation in the manufacturing process.
  • Create and understand documentation as it relates to technical discipline (e.g., specifications, validations, prototypes, technical manuals, 3D Models/schematics/equipment drawings/BOM’s).
  • Submit specification, protocol and report for approvals and documentation control via a Change Request.
  • Develop comprehensive software validations and/or equipment installation qualification protocols per the specification.
  • Execute software validation and/or qualification protocols & record results.
  • Document, communicate and follow-up on software/equipment issues.
  • Create documents, links and Change Requests utilizing a Product Data Management system.



  • 1-3 years of experience.
  • Experience in Medical Device is desirable.
  • Mechanical Engineering background
  • Excellent analytical, system analysis, planning and problem-solving skills.
  • Ability to acquire new skills quickly and thrives in a fast paced, collaborative team environment.
  • Good knowledge of Excel and other MS Office tools.
  • Strong knowledge in French and English

Apply now:

In addition, for this exciting job we offer you an attractive compensation package, very good opportunities for personal and professional development through our established talent management program. Above all, you will have the opportunity to become part of a culture where everyone contributes to improving people's lives at all levels. Please let us know more about yourself by applying in English and clicking on the link below.

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