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Principal Design Quality / Qualité de conception principale

Boston Scientific Gruppe

Montreal

On-site

CAD 95,000 - 190,000

Full time

3 days ago
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Job summary

A leading medical device company seeks a Principal Design Quality Engineer in Montreal. The role involves enhancing product development through quality improvements and compliance initiatives. Ideal candidates will possess strong engineering backgrounds and experience in quality assurance, coupled with excellent problem-solving and communication skills.

Qualifications

  • 7+ years of relevant work experience in quality assurance in medical devices.
  • Strong communication skills and attention to detail.

Responsibilities

  • Develops quality-engineering methodologies for cardiovascular products.
  • Provides quality compliance input to project teams.
  • Supports internal and external regulatory audits.

Skills

Quality Assurance
Problem Solving
Collaboration
Compliance
Communication

Education

Bachelor’s degree in mechanical, electrical, or biomedical engineering

Job description

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Onsite Location(s):

Montreal, QC, CA

Additional Locations:Canada-QC-Montreal

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About the role

The ideal Principal Design Quality Engineer will bring their leadership to new product development projects and sustaining projects for our innovative cardiovascular products. Furthermore, they will develop, establish, and maintain quality-engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements.

Your responsibilities will include:

Develops understanding of design controls, risk management, and usability for medical devices

Provides quality and compliance input to project teams for project decisions and deliverables (e.g., design change analysis, design inputs, design outputs, test methods, design reviews, design verification and validation, usability testing, software validation, process validation, and labeling)

Provides quality and compliance input for post-market product sustaining activities, such as design changes, NCEPs, CAPAs, PIRs, field signal evaluations, and field actions

Applies technical skills including sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues

Responsible for collaborating within a team to identify and implement effective controls to support development or maintenance of products to meet internal and external requirements

Builds quality into all aspects of work by maintaining compliance with all quality requirements

Supports internal and external regulatory audits as required

Performs other duties as necessary or as required by the organization

Required qualifications:

  • Bachelor’s degree in mechanical, electrical, or biomedical engineering, or equivalent.
  • 7+ years of relevant work experience relating to quality assurance in a highly regulated industry (ideally medical devices)

Preferred Qualifications

  • Focus on detailed work with emphasis on accuracy and completeness
  • Excellent organizational and planning skills; drives for results
  • Strong communication (oral and written) and presentation skills
  • High energy problem solver capable of driving items to closure
  • Ability to collaborate and work on a global team

Our organization is across Canada and has commercial representation in 140 countries.

This job involves regular collaboration with colleagues, clients, and stakeholders across Canada, the U.S., and/or internationally, making proficiency in English essential for effective communication and alignment. English is necessary for engaging with a range of documentation and maintaining effective communication if interacting with external clients or vendors.

As detailed in the job description, this job involves communicating, both verbally and in writing, with other Boston Scientific teams located across Canada, the United States and/or with our international clients and partners. International customers and partners represent an important part of our activities. Based on an evaluation, we have determined that the duties of the Principal Design Quality Engineer position require knowledge of English in addition to French (oral and written). We also determined that the English language skills already required of other employees do not permit the performance of English language skills tasks related to QPrincipal Design Quality Engineer position.

However, in Québec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language than French. Boston Scientific solely requires proficiency in English where it is necessary for the performance of an employee’s duties.

Requisition ID:604156

Minimum Salary: $95600

Maximum Salary: $189800

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com --will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for hourly, non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for salaried, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for sales roles is governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!


Job Segment: Biomedical Engineering, Quality Engineer, Compliance, Medical Device, Testing, Engineering, Legal, Healthcare, Technology

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