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Eurofins

Global lab testing and analytics network

QA Associate

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeToronto, ON, Canada

About the Job

Requirements

  • Requires 1–2 years of experience in a Good Manufacturing Practices (GMP) environment.
  • Experience with pharmaceuticals, natural health products, or medical devices is an asset.
  • Experience working directly with pharmaceutical products is an asset.
  • Experience working in a contract laboratory is considered an asset.
  • Ability to communicate fluently in French, verbally and in writing, to engage with clients and stakeholders.
  • A solid background and understanding of Chemistry or Microbiology is mandatory.
  • Proficiency with Microsoft Office, especially Excel.
  • Willingness and ability to travel within Canada for business trips.

Responsibilities

  • Review Good Manufacturing Practices (GMP) documents, including master production documents.
  • Reconcile GMP documents for product lots requiring quality-control disposition, including batch records, Certificates of Analysis and Manufacture, and product label reviews.
  • Coordinate product release to ensure products are of good quality and comply with GMPs.
  • Implement Canadian confirmatory testing for imported products.
  • Review warehouse reports.
  • Ensure products received are transported, handled, sampled, stored, and destroyed correctly.
  • Maintain familiarity with client contracts, including agreed responsibilities, and client establishment licences, including approved foreign sites.
  • Assess, trend, and evaluate product stability programs to ensure compliance.
  • Assist with deviations and out-of-specification investigations, Corrective and Preventive Action investigations, change controls, and the evaluation and documentation of change controls.
  • Assist with evaluation of complaints, reporting of adverse events, and recalls.
  • Assess the disposition of damaged and returned goods.
  • Assist with protocols and reports for transportation validation, warehouse temperature mapping, or stability studies.
  • Assist with self-inspections and external inspections.
  • Track and maintain GMP documents.
  • Initiate and assist with updates to clients’ Standard Operating Procedures (SOPs).
  • Support staff SOP training and ensure training records are compliant.
  • Adhere to clients’ SOPs and attend audits on behalf of clients, ensuring a thorough understanding of client needs and requirements.
  • Meet the company’s service standards.
  • Maintain accurate inventory control and distribution records.
  • Attend staff meetings and perform other duties delegated by management.

Desired Qualifications

  • Experience working with pharmaceuticals, natural health products, or medical devices.
  • Experience working directly with pharmaceutical products.
  • Experience working in a contract laboratory.
  • A Bachelor's degree, preferably in Chemistry, Microbiology, or Biochemistry, or a diploma in a related field.
  • A diploma or certificate in Quality Operations of pharmaceutical products.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size
10,001+
Company stage
IPO
Headquarters
Luxembourg
Founded
1987

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