Company Description
Eurofins Scientific is an international network of independent life sciences companies, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In under 40 years, Eurofins has grown from one laboratory in Nantes, France to over 65,000 employees across a decentralised and entrepreneurial network of over 950 laboratories in over 1,000 independent companies across 57 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

The Eurofins network generated EUR 7.296 billion revenues in FY 2025, and has been one of the fastest growing listed European companies for almost three decades.

Job Description
This position is responsible for ensuring compliance with applicable regulations (i.e. ISO 17025, GMP, GLP), for clients requiring quality assurance services.

Responsibilities:

Review and determine the status of the quality documents (including, but not limited to, raw laboratory data, validation studies, logbooks, and calibration reports)

Providing support with maintaining Quality System, including drafting and updating quality procedures

Assisting with internal and external audits

Ensuring that all reports and accompanying raw data are according to GMP and ISO 17025,



accurate, correct and acceptable according to the study protocol, methods and relevant SOPs

Interacting with department staff to acquire information for report writing and auditing purposes and present information to staff regarding deficiencies and areas of improvement

Log and review complaints; compile required ISO 17025/ GMP documents for the evaluation of complaints

Perform and manage the internal auditing program if required

Manage the ongoing tracking and maintenance of GMP and ISO 17025 documents

Support the training of new staff

Evaluate and summarize instrumentation data in final reports

General record-keeping practices according to local and global SOPs

Review training records and generate associated reports if required

Initiate and conduct deviations and out-of-specification investigations

Initiate and conduct Corrective Action and Preventative Action (CAPA) investigations

Initiate and assist in Change Control procedures

Adhere to the Standard Operating Procedures

Circulate Standard Operating Procedures and follow up on training requirements

Ensure that all staff members are following the Standard Operating Procedures at all times

Assist with the maintenance of ISO 17025 and GMP accreditation

Attend staff meetings

Any other duties as delegated by the Department Head or designated

Additional Information
Please note that relocation to Mississauga, ON is expected in 2026.

At Eurofins we offer excellent full time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.

As a Eurofins employee,



you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.ca

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

This posting is for a current vacancy and the successful candidate will start as soon as possible.

Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process.

NO AGENCIES, CALLS OR EMAILS PLEASE

Key Skills, Experience & Abilities:

Knowledge of ISO 17025 and GMP requirements

GMP experience will be an added asset

Must speak and write English fluently

Must possess excellent communication skills, both written and verbal

Must be articulate

Excellent organizational skills

High level of accuracy and strong attention to detail

Ability to work independently, while supporting a collaborative, team-based department

Ability to multitask and remain calm under pressure

High level of professionalism, maturity, good judgment, and discretion when dealing in confidential matters

Exceptional computer skills with a high level of competence with MS Office (Outlook, Word, Excel)

Must be proactive, self-disciplined, and able to demonstrate a high level of productivity

Demonstrate satisfactory work performance and attendance record

Willingness to learn with the ability to retain information quickly and apply knowledge to various scenarios

Education:

Degree or diploma in a science-related discipline

Computer proficiency in Microsoft Office, especially Excel

Working Conditions:

This position will be working in office and lab environments. Moderate level of activity and some light lifting requirements to fulfill any required duties. Evening or weekend work may occasionally be required.

📌 QA Reviewer - Eurofins BioPharma Product Testing Toronto, Inc. (Ontario)
🏢 Eurofins
📍 Ontario