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Eurofins

Verified Job Source

With over 65,000 staff across 59 countries, Eurofins provides testing, inspection, and certification services.

Luxembourg, Luxembourg

Biotechnology Research
5,001+ people

About

Since 1987, Eurofins has grown from one laboratory in Nantes, France to over 65,000 staff across a network of independent companies in 59 countries, operating over 950 laboratories. Performing over 450 million tests every year, Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. Ever since its IPO on the French stock exchange in 1997, Eurofins has been one of the fastest growing listed European companies.

Open positions

QA Reviewer - Eurofins BioPharma Product Testing Toronto, Inc.

On-site · Toronto

The role is responsible for ensuring compliance with ISO 17025, GMP, and GLP regulations through the review of quality documents and laboratory data. Key duties include managing internal audits, conducting CAPA investigations, and maintaining the Quality System and SOPs.

Cash Application Clerk - Eurofins NSC Canada, Inc.

On-site · Toronto

The Cash Application Clerk is responsible for applying cash receipts across multiple business lines and preparing electronic bank deposits. They also manage customer statements, create historical aging reports, and respond to business unit inquiries.

QA Associate - Eurofins BioPharma Product Testing Toronto, Inc.

On-site · Toronto

The QA Associate provides documentation and technical support for clients, focusing on the review and reconciliation of GMP documents and product lot disposition. They are responsible for coordinating product release, managing CAPAs, and assisting with stability programs and external inspections.

Manager, Drug Product Operations & Engineering - Eurofins CDMO Alphora, Inc.

On-site · Mississauga

Lead Drug Product manufacturing operations and engineering teams to ensure successful production of clinical-stage pharmaceutical products. Drive operational excellence, manage client relationships, and oversee technical initiatives including process development and equipment qualification.

QA Associate – Biologics - Eurofins CDMO Alphora, Inc.

On-site · Mississauga

The QA Associate provides quality oversight for GMP activities, including batch manufacturing, fill-finish operations, and analytical testing. They are responsible for reviewing batch records, managing deviations and investigations, and ensuring compliance with regulatory standards.

Business Development Executive, Drug Product - Eurofins CDMO Alphora, Inc.

On-site · Mississauga

The Business Development Executive will focus on identifying opportunities, expanding customer relationships, and positioning Alphora as a trusted development and manufacturing partner. Key responsibilities include developing strategic business plans, managing client interactions, and collaborating with internal teams to deliver exceptional customer experiences.

Accounts Payable Clerk (Bilingual) - Eurofins NSC Canada, Inc.

On-site · Toronto

The Accounts Payable Clerk will perform core day-to-day accounts payable activities as part of the Shared Services team. Responsibilities include reviewing invoices, coding and entering vendor invoices, processing payments, and maintaining vendor files.

Warehouse Technician - Eurofins CDMO Alphora, Inc.

On-site · Oakville

The Warehouse Technician will support warehouse operations by ensuring compliance with cGMP standards and managing material handling. Responsibilities include receiving and staging raw materials, maintaining safety protocols, and supporting shipping logistics.

Scientist III – Mass Spectrometry - Eurofins PSS Canada, Inc.

On-site · Toronto

The Scientist III will apply scientific expertise to select appropriate assays for the characterization and quality control of vaccines and other products. This includes developing test methods for release, stability, and characterization assays for new vaccine products.