Senior Quality Assurance Associate, Systems

Posted 8 Days Ago
Be an Early Applicant
Burnaby, BC, CAN
In-Office
73K-98K Annually
Senior level
Biotech
The Role
Lead and execute QA systems activities including nonconformance, CAPA, SCAR, change control, investigations, and internal/external audits. Maintain compliant quality documentation, analyze QMS data and KPIs, partner cross-functionally to ensure regulatory compliance (ISO, CE, cGMP), and recommend process improvements to uphold product quality.
Summary Generated by Built In
Job Description Summary

STEMCELL Technologies is searching for a Senior Quality Assurance (QA) Associate to join our QA Systems team!
As a Senior QA Associate, you will contribute to upholding quality standards and regulatory compliance by performing key quality activities, maintaining quality documentation, and recommending continuous improvement initiatives. You will apply independent judgment to evaluate complex quality issues and implement effective solutions using current industry practices and methodologies. Through your expertise, you will help ensure that all products meet specified quality requirements and regulatory standards, contributing significantly to STEMCELL’s commitment to quality and compliance.

Job Description

Duties and Responsibilities

  • Perform key quality activities, focusing on nonconformance and corrective and preventive actions (CAPA) systems while supporting supplier corrective action requests (SCAR), change control, audit, and document management to maintain quality standards and ensure regulatory compliance
  • Conduct and facilitate investigations using industry standard methods for root cause determinations and identification of meaningful corrective and preventative actions
  • Conduct internal and external audits to assess compliance with applicable standards, regulations, directives, and organizational policies
  • Partner with cross-functional teams to ensure Quality Management System (QMS) compliance, analyze quality data (e.g., inspections, testing, audits, CAPA metrics, and quality key performance indicators), and recommend process improvements
  • Maintain accurate, complete, and compliant quality documentation, including policies, procedures, records, and quality system activities in accordance with regulatory requirements

Knowledge and Qualifications

  • Bachelor’s Degree in Life Sciences (e.g., Chemistry, Biology) or related field with 2-6 years of relevant QA experience
  • Knowledge of QMS, including nonconformance, CAPA, SCAR, change control, and document control
  • Solid understanding of regulatory requirements and industry standards, including ISO 9001, ISO 13485, CE medical/IVD device directives, and cGMP, with the ability to interpret and apply technical documents, procedures, and regulations
  • Demonstrated ability to coordinate QA responsibilities, maintain accurate quality and regulatory documentation, manage multiple priorities in a fast-paced environment, and apply strong organizational, project, and time management skills
  • Excellent communication, technical report writing, presentation, interpersonal, and cross-functional collaboration skills, with a self-motivated, independent work ethic and a willingness to learn and take on new responsibilities

#LI-KK1 #LI-Onsite

STEMCELL Technologies is a privately owned, Vancouver-based biotechnology company that helps power leading-edge life science research around the world. Driven by our love of science and passion for quality, we are a company of Scientists Helping Scientists—standing by our customers to provide the outstanding products, technical support, and training they need to advance their research. Scientists performing stem cell, immunology, cancer, regenerative medicine, and cellular therapy research are among those who rely on our cell culture media, cell separation products, instruments, accessory products, and services. Through our many regional offices, as well as our distribution centers in Vancouver, Seattle, Grenoble, and Singapore, we deliver our innovative, specialized products to more than 100 countries. With over 1,800 employees globally, most with scientific or engineering degrees, STEMCELL is proud to be the largest biotechnology employer in Canada.

This is an opportunity to work with highly motivated colleagues in a science-oriented, creative, and dynamic environment. We offer a competitive salary, excellent benefits, and meaningful career development opportunities.

STEMCELL is well recognized for exceptional leadership and business practices. We are one of Canada’s Best Managed Companies and operate an ISO 14001-certified environmental management system to measure and reduce our environmental impact. 

As an equal opportunity employer, STEMCELL is dedicated to ensuring that every employee feels safe, valued, and respected for who they are. We know that scientific progress and innovation occur when diverse, creative minds come together and we are committed to nurturing a culture of inclusivity and belonging. STEMCELL enforces a zero-tolerance policy for any form of discrimination. Selection decisions are solely based on job-related factors.

The annual salary for this job ranges from:

$72,700.00 - $98,300.00

STEMCELL determines an individual’s pay within the range based on multiple factors including experience, education, job-related skills, and equity within the team or organization. For jobs that are eligible for sales incentives, the range noted above is inclusive of target incentives; actual incentives are based on individual performance results in accordance with company policy. In addition to base salary, STEMCELL offers a comprehensive total rewards package including health benefits, retirement savings, and more.

To apply, please select the “Apply” button below. You will then be directed to a login screen asking you to set up an account, which is required to apply.​​

Skills Required

  • Bachelor's degree in Life Sciences or related field
  • 2-6 years relevant Quality Assurance experience
  • Knowledge and hands-on experience with QMS, nonconformance, CAPA, SCAR, change control, and document control
  • Understanding and ability to apply regulatory standards: ISO 9001, ISO 13485, CE medical/IVD directives, and cGMP
  • Experience conducting investigations and root cause analysis and implementing corrective/preventive actions
  • Experience performing internal and external audits
  • Strong communication, technical report writing, presentation, and cross-functional collaboration skills
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The Company
HQ: Vancouver, British Columbia
2,000 Employees
Year Founded: 1993

What We Do

STEMCELL Technologies is a Canadian biotechnology company that helps power leading-edge life science research around the world. Driven by our love of science and passion for quality, we are Scientists Helping Scientists—standing by our customers to provide the outstanding products, technical support, and training they need to advance their research. Scientists performing stem cell, immunology, cancer, regenerative medicine, and cellular therapy research are among those who rely on our cell culture media, cell separation products, instruments, accessory products, and services. Since the launch of the company by Dr. Allen Eaves in 1993, STEMCELL has reinvested all profits back into the research and development of products to better support the international research community. Today, STEMCELL is the largest biotech company in Canada, with over 2000 employees globally, most with scientific or engineering degrees. Through our many regional offices, as well as our distribution centers in Vancouver, Seattle, Grenoble, and Singapore, we deliver our innovative, specialized products to more than 70 countries. At STEMCELL, we are dedicated to improving lives through advancing knowledge and scientific discovery, through our commitment to fostering diversity and inclusion in STEM and the life sciences industry, and through our investments in sustainability, community, and social responsibility. We do all this because we love science as much as you do.

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