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 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Eurofins BioPharma Product Testing Toronto, Inc. is seeking a detail-oriented and analytical Analyst II R&D to join our Research and Development team in Toronto, Canada. In this role, you will support the development and validation of analytical methods for pharmaceutical products, ensuring quality, safety, and regulatory compliance. You will work collaboratively with cross-functional teams to conduct testing, analyze data, and contribute to the advancement of our product portfolio.

Key Responsibilities:

Develop, validate, verify, and transfer analytical methods for assay and impurities testing in accordance with ICH and regulatory guidelines.

Perform routine and validation analysis using advanced analytical instrumentation including HPLC, GC, LC-MS/MS, and GC-MS/MS.

Conduct analytical testing and quality control procedures on pharmaceutical products using appropriate laboratory techniques.

Analyze and interpret complex analytical data, ensuring accuracy, completeness, and compliance with documentation standards.

Prepare and review method validation/verification/transfer protocols and final reports with precision and clarity.

Troubleshoot analytical methods and resolve technical issues to ensure consistent and reliable results.

Support and conduct OOS/OOT investigations and assist in identifying root causes and corrective actions.

Coordinate method transfer studies between clients and internal departments to ensure successful implementation and reproducibility of methods.

Maintain accurate and organized laboratory records, ensuring full traceability and compliance with regulatory requirements.

Review technical documents, data packages, and proposals as required.

Collaborate with R&D scientists, Quality Assurance, and project managers to support product development initiatives.

Assist with SOP training for new personnel and support SOP revisions as needed.

Liaise with clients to maintain strong professional relationships and provide technical support.

Provide ongoing technical guidance and training to staff to strengthen departmental capabilities.

Stay current with emerging technologies, industry best practices, and regulatory updates relevant to pharmaceutical testing.

Support the R&D Manager in departmental operations to ensure smooth workflow and achievement of business goals.

Qualifications

Required Qualifications:

Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline5-10 years of hands-on experience in pharmaceutical R&D, product testing, or analytical laboratory environmentsStrong proficiency in analytical techniques and familiarity with laboratory instrumentation (HPLC, GC, mass spectrometry, or similar)Solid understanding of pharmaceutical quality control procedures and regulatory compliance standards (GMP/GLP)Excellent analytical and problem-solving skills with strong attention to detailProficiency in data analysis and statistical methodsStrong technical writing and documentation skillsAbility to work independently and collaboratively in a team-oriented environmentOrganized and efficient approach to managing multiple projects and priorities

Preferred Qualifications:

Experience with analytical method development and validationFamiliarity with laboratory information management systems (LIMS)Knowledge of pharmaceutical regulatory requirements and industry standardsExperience with quality assurance and continuous improvement initiativesAdvanced proficiency in data analysis software or statistical toolsCertification in pharmaceutical quality or related field

WORKING CONDITIONS: 

This position will be working in a laboratory environment where standing is required for greater than 50% of the time. Light lifting requirements of no more than 30 lbs. Hazardous materials are handled using established safety procedures and appropriate PPE. Shift work and overtime may be required, as well as working periodic weekends and/or evenings.

Additional Information

Please note that relocation to Mississauga, ON is expected in mid-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.

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