QA Reviewer - Eurofins BioPharma Product Testing Inc.

QA Reviewer - Eurofins Bio Pharma Product Testing Toronto, Inc.

Full-time

Compensation: up to CAD 50000 - yearly

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.

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

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…