Company Description

Eurofins Scientific is an international life sciences company, 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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.

In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

This position is responsible for ensuring compliance with applicable regulations (i.e. Cosmetics Regulations, Food and Drugs Act and Regulations, Natural Health Products Regulations, FDA, EMA, etc.), 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, qualification and calibration reports).
• Review and release of laboratory results.
• Review out-of-specification, out-of-trend and other investigations
• Providing support with maintaining Quality System, including drafting and updating quality procedures.
• Perform technical writing tasks such as Method Validation Protocols
• Assisting with internal and external audits.
• Ensuring that all reports and accompanying raw data are according to GMP, 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 GMP documents for the evaluation of complaints.
• Perform and manage the internal auditing program if required.
• Manage the ongoing tracking and maintenance of GMP documents
• Develop, review and revise training materials. Assist in training of new staff.
• Evaluate and summarize instrumentation data in final reports.
• General record-keeping practices according to local and global SOPs including maintenance of on- and off-site archive.
• Assist in issuing logbooks and forms when needed.
• Review training records and generate associated reports if required.
• Initiate and investigate deviations if required.
• Perform risk assessment pertaining to discovered deviations.
• Initiate and conduct Corrective Action and Preventative Action (CAPA) plans.
• Initiate and assist in Change Control procedures.
• Assist in and perform trending and prepare reports as per relevant procedures.
• Adhere to the Standard Operating Procedures.
• Circulate Standard Operating Procedures and follow up on training requirements.
• Ensure that all staff members are always following the Standard Operating Procedures.
• Assist with the maintenance of Health Canada and FDA accreditation.
• Assist in summarizing information and report preparation for Management Review.
• Attend staff meetings.
• Any other duties as delegated by the Quality Assurance Manager or designate.

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