Skip to main content
Post your resume and find your next job on Indeed!

Quality Engineer Medical Device jobs

Sort by: -
    • This involves managing and executing quality assurance program activities, internally auditing Flowserve Toronto’s quality assurance program for regulatory,…
    • Use quality tools to establish root cause.
    • Benefits - Our group benefit plan covers medical, dental, vision, and other health needs, including our employee…
    • Analyze data to develop, monitor and communicate quality performance metrics to drive CI projects and maintain acceptable part quality.
    • Proven experience in quality assurance or quality engineering, preferably in endpoint management or device management solutions.
    • View all Scotiabank jobs - Toronto jobs
    • Salary Search: Senior Quality Engineer salaries in Toronto, ON
    • See popular questions & answers about Scotiabank
    • Il s’agit d’un travail en installations technologiques lié à l’exploitation de systèmes et d’équipement contrôlés par microprocesseur dans des établissements de…
    • Develop and maintain quality procedures, work instructions, and quality documentation.
    • This role is ideal for an engineer with experience in nuclear quality…
    • 3+ years of QA experience in the pharmaceutical or medical device industry.
    • Expertise in electronic quality management systems (QMS) and QMS product management…
    • Track and resolve quality issues related to new product introductions; develop control plans and customer‑required quality documentation.
    • Participate in the design and development of medical devices while following a quality system in accordance with ISO 13485.
    • Job Types: Full-time, Permanent.
    • Maintain quality records and documentation control.
    • 100% employer-paid medical and dental benefits as of day 1.
    • Les non-conformités techniques majeures.
    • Minimum 10 years of engineering and project management experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing…
  • View similar jobs with this employer
    • Provide and document quality-related training and maintain training and quality records in accordance with company procedures and regulatory requirements.
    • Utilize customer portals to obtain quality requirements and submit required quality documentation.
    • Attention to detail and commitment to quality.
    • Collect data of Internal NCRs and input in tracking system.
    • Perform Root cause Analysis -by data collection and pictorial tools such as “Fishbone Diagram” and “…
    • Methods in collaboration with engineering and quality teams.
    • Develop/specify standards, methods, procedures to determine product quality/release readiness.
Get e-mail updates for the latest Quality Engineer Medical Device jobs

By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.

People also searched:

engineering

Career Resources:

Flowserve logo
Nuclear QA Engineer
Woodbridge, ON
$101,049.82–$151,574.74 a year

Job details

$101,049.82–$151,574.74 a year
Monday to Friday
Woodbridge, ON

Full job description

COMPANY OVERVIEW:

Flowserve is the recognized world leader in supplying pumps, valves, seals, automation, and services to the power, oil, gas, chemical, and other industries. With more than 18,000 employees in more than 55 countries, we combine our global reach with a local presence.

If a culture of excellence, innovation and ownership is what you’re searching for, consider putting your experience in motion at Flowserve. As an individual contributor, or as a leader of people, your enterprise mindset will ensure Flowserve’s position as the global standard in comprehensive flow control solutions. Here, your opportunity for professional development and industry leading rewards will be supported by our foundational commitments to the values of people first, integrity and safety. Thinking beyond opportunity and reward, at Flowserve, we are inspired by working together to create extraordinary flow control solutions to make the world better for everyone!

If you would enjoy working for a people focused corporation with strong Values and Behaviors that drive business decisions, then Flowserve is the place for you.

Flowserve Values: People, Safety, Integrity, Innovation, Ownership, and Excellence.

Flowserve Behaviors: Enterprise Mindset, Deliver Beyond Expectations, Act and Learn, Trust and Respect, Be Safe, Embrace change, and Act with Integrity.

ROLE SUMMARY:

The Senior Quality Assurance Engineer at Flowserve is tasked with ensuring that all products, processes, and services within Flowserve’s Toronto Quick Response Center (QRC) facility producing products for the nuclear industry or related industry meet stringent quality and safety standards. This involves managing and executing quality assurance program activities, internally auditing Flowserve Toronto’s quality assurance program for regulatory, customer, and Flowserve compliance, implementing quality assurance programs aligned to industry or customer expectations, identifying and resolving programmatic non-conformances or quality notifications, and supporting Nuclear product growth initiatives. This position requires a comprehensive understanding of nuclear safety principles, quality assurance methodologies, and international Nuclear standard / code requirements. Travel is expected to be less than 10% however, travel may be expected up to 20% periodically.

PRIMARY RESPONSBILITIES

  • Program Maintenance: Ensure Toronto QMS compliance with nuclear industry and customer standards and regulations. This includes internal auditing, support with site regulatory or customer audits/surveys, and corrective actions on findings to determine the effectiveness of the QA Program.
  • Quality Assurance and Control: Develop, implement, and maintain quality assurance protocols for nuclear projects and programs.
  • Coordinate with production in order to plan and execute inbound and production inspection activities.
  • Collaborate with the department or other company departments to clarify / resolve issues or techniques related to QC activities.
  • Regulatory Compliance: Keep abreast of changes in regulations and update quality protocols accordingly. Highlight to leadership changes coming in the industry and its impact or opportunity to Flowserve Toronto’s nuclear manufacturing strategy. Responsible for managing site QMS.
  • Risk Management: Identify potential risks in nuclear projects and develop strategies to mitigate these risks. Conduct risk assessments and implement corrective actions as needed.
  • Continuous Improvement: Lead initiatives for continuous improvement in nuclear quality standards. Analyze data to identify areas for improvement and implement solutions to enhance overall project quality.
  • Training and Development: Develop and deliver training programs to enhance the quality skills of the site. Ensure that all identified personnel are knowledgeable about quality standards and protocols.
  • Documentation: Maintain detailed records of quality assurance activities, including purchased product incoming documents, final document reviews of shipments, audit reports, findings, and corrective actions. Ensure that all documentation is accurate and accessible through enterprise quality systems.
  • Review and approve purchase orders for applicable materials, parts, components, and other items for quality assurance requirement compliance.
  • Develop the ITP with engineering alignment.
  • Review and approve document packages for customer release.
  • Stakeholder Engagement: Work closely with stakeholders, including clients, regulatory bodies, and internal teams, to ensure transparency and alignment on quality objectives.
  • Lead site-wide efforts to drive process and product defects out of the daily work activities and deliverables. Implement an effective root-cause analysis and corrective action management program to ensure causes of defects and escapes are thoroughly understood and corrective and preventative actions are implemented and sustained. Drive the adoption of poka-yoke solutions where possible.
  • Participate in external supplier quality surveillance activities and audits.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Bachelor’s degree in Quality Management, Nuclear Engineering, Mechanical Engineering, or equivalent industry experience
  • Experience: Minimum of 5+ years of experience in nuclear quality assurance or a related field.
  • At least five years of demonstrated success leading a nuclear quality program that meets the requirements of CSA N299.
  • At least five years of experience with accepting/approving NDE (such as LPI, RT, MT, PMI, UT).
  • Technical Skills: Proficiency in quality assurance methodologies (including print reading and GD&T understanding), regulatory compliance, and risk management. Familiarity with nuclear engineering principles and technologies.
  • Analytical Skills: Strong analytical and problem-solving skills. Ability to interpret complex data and make informed decisions.
  • Communication Skills: Excellent verbal and written communication skills. Ability to convey technical information clearly and effectively to diverse audiences.
  • Attention to Detail: Meticulous attention to detail and a commitment to maintaining high-quality standards.
  • Adaptability: Ability to adapt to changing regulations and project requirements. Flexibility to work in diverse and challenging environments.

PREFERRED EXPERIENCE/SKILLS:

Add site level preferences in this section

  • Experience with international nuclear standards such as: ASME, CSA, ISO 19443 codes and standards and other relevant industry regulations is preferred.
  • Familiar with Commercial Grade Dedication and material upgrade requirements
  • Nuclear audit experience to CSA N285; CSA N299; 10 CFR 50 App. B; NQA-1 and has maintained Lead Auditor Certification
  • At least five years of demonstrated success leading a nuclear quality program that meets the requirements of ASME BPVC Sections II and III, 10 CFR 50 Appendix B, and ASME NQA-1, as well as ISO 9001.
  • ASQ CQA, NQA-1 Lead Auditor, or similar.
  • ASQ CQE
  • CIP Green Belt training and/or Lean Manufacturing experience.
  • Experience with CMM related inspection methodologies.

SITE SPECIFIC DETAILS

  • On site in Toronto, ON
  • Standard office hours: 8:00AM – 4:30PM, Mon-Fri, including occasional Saturdays

The pay range for this role is $101,049.82 - $151,574.74 CAD Annual.

Let Employers Find YouUpload Your Resume