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Eurofins

Global lab testing and analytics network

QA Reviewer

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

About the Job

Requirements

  • Knowledge of ISO 17025 and Good Manufacturing Practice (GMP) requirements.
  • Must speak and write English fluently.
  • Must possess excellent communication skills, both written and verbal.
  • Must be articulate.
  • Must have excellent organizational skills.
  • Must demonstrate a high level of accuracy and strong attention to detail.
  • Must be able to work independently while supporting a collaborative, team-based department.
  • Must be able to multitask and remain calm under pressure.
  • Must demonstrate professionalism, maturity, good judgment, and discretion when dealing with confidential matters.
  • Must have strong computer skills, including competence with Microsoft Office (Outlook, Word, and Excel).
  • Must be proactive, self-disciplined, and able to demonstrate a high level of productivity.
  • Must demonstrate satisfactory work performance and attendance record.
  • Must be willing to learn, retain information quickly, and apply knowledge to various scenarios.
  • Must have a degree or diploma in a science-related discipline.
  • Must be proficient in Microsoft Office, especially Excel.
  • Must be able to perform moderate activity and some light lifting as required.
  • Must be willing to work occasional evenings or weekends.

Responsibilities

  • Review quality documents, including raw laboratory data, validation studies, logbooks, and calibration reports, and determine their status.
  • Support maintenance of the Quality System, including drafting and updating quality procedures.
  • Assist with internal and external audits.
  • Ensure reports and accompanying raw data are accurate, correct, and acceptable according to GMP, ISO 17025, study protocols, methods, and relevant Standard Operating Procedures (SOPs).
  • Interact with department staff to obtain information for report writing and auditing, and present information to staff regarding deficiencies and areas for improvement.
  • Log and review complaints, and compile required ISO 17025 and GMP documents for complaint evaluation.
  • Perform and manage the internal auditing program when required.
  • Manage ongoing tracking and maintenance of GMP and ISO 17025 documents.
  • Support training of new staff.
  • Evaluate and summarize instrumentation data in final reports.
  • Maintain records according to local and global SOPs.
  • Review training records and generate associated reports when required.
  • Initiate and conduct deviation and out-of-specification investigations.
  • Initiate and conduct Corrective Action and Preventative Action (CAPA) investigations.
  • Initiate and assist with Change Control procedures.
  • Adhere to SOPs.
  • Circulate SOPs and follow up on training requirements.
  • Ensure all staff members follow SOPs.
  • Assist with maintaining ISO 17025 and GMP accreditation.
  • Attend staff meetings.
  • Perform other duties as delegated by the Department Head or designated person.

Desired Qualifications

  • GMP experience is an added asset.

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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