CAPA Analyst (Quality Systems Associate) - 28441BR - EN in Burnaby at Stryker Corporation

Date Posted: 4/14/2018

Job Snapshot

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    Regulatory Affairs
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    Not Specified
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Job Description

At Stryker, customers and patients are at the heart of everything we do. We proudly stand behind our quality products. If you are passionate about improving quality in production, and want to grow with a growing company that is consistently ranked by Forbes as one of the Top 100 Companies to Work For, we have the right opportunity for you.

We have an opportunity for a collaborative CAPA Analyst (akin to Quality Analyst or Quality Systems Associate) who is passionate about coaching and guiding cross-functional team members through the corrective/preventive actions (CAPA) process. Through these interactions, the CAPA Analyst will gain wide exposure to all levels and parts of the organization.

The CAPA Analyst is responsible for reviewing and evaluating CAPA and the CAPA effectiveness program, as well as communicating CAPA status to cross-functional departments and management.

  • Participate in identifying the need for a CAPA to address non-conformances.
  • Develop / review metrics for adverse trending analysis of non-conformities.
  • Support cross-functional teams in the investigations of non-conforming events and CAPA implementation.
  • Review and evaluate CAPAs associated with non-conformance and regulatory audits.
  • Review CAPAs to determine their effectiveness.
  • Develop and provide metrics for CAPA status.
  • Ensure on-time completion of CAPAs.
  • Identify opportunities for continuous improvement.
  • Interact with FDA and other regulatory agencies, as required.
  • Create / revise SOPs associated with CAPA systems.
  • Provide training for compliance to CAPA procedures.

Job Requirements

  • B.S. / M.S. in engineering or sciences (mechanical, electrical, industrial, software, computer, biology, physics, chemistry, etc. )
  • 1 to 2 years experience
  • Strong ability to influence, motivate, and drive action
  • Ability to convince others to invest the time and energy on activities that are outside their normal or ideal workflow
  • Ability to balance firmness with diplomacy and supportiveness
  • Able to read and interpret engineering schematics/drawing/prints, preferred
  • Commitment to excellence and high standards
  • Excellent English written and oral communication skills
  • Excellent organizational, problem-solving, and analytical skills that lead to sound, timely decisions
  • Ability and versatility to manage changing priorities and workflow for multiple projects and deadlines
  • Ability to deal effectively with a diversity of individuals at all organizational levels
  • Working knowledge of data collection, data analysis, evaluation, and scientific method
  • Must be able to analyze and resolve non-routine product issues using independent judgment with the assistance of Quality and Engineering support when required
  • Preferably have knowledge of applicable international regulations and standards (QSR, MDD, ISO 13485, CMDCAS, etc.)
  • Willingness to train others in quality assurance/GMP-related topics
  • Proficient with Microsoft Office
About Stryker

Stryker is one of the world’s leading medical technology companies and consistently ranked as one of the Top 100 Employers to Work For by Forbes. Together with our customers, we are driven to make healthcare better. The Company offers a diverse array of innovative medical technologies, including orthopaedics, medical and surgical, and neurotechnology & spine products to help people lead more active and more satisfying lives. Stryker products and services are available in over 100 countries around the world. For more information, please visit our website at

To learn more about why people love working at Stryker, check out this video:


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