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up to $47k per year
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In office (Oakville)
Seniority
Junior
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Eurofins Scientific is a laboratory testing group founded in 1987 to commercialise a method for authenticating the origin of wines and foods, and it has since become one of the largest bioanalytical testing networks in the world. It runs thousands of laboratories offering food and feed testing, environmental analysis, pharmaceutical and biopharma product testing, agroscience services, clinical diagnostics and consumer product certification. The group is registered in Luxembourg, listed in Paris, and has grown almost entirely by acquiring and integrating specialist laboratories across more than sixty countries.

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.

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Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -“API’s”) as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths.

Eurofins CDMO Alphora Inc. is a leading contract development and manufacturing organization specializing in complex active pharmaceutical ingredients (APIs). We are looking for a driven Process Specialist to join our Technology Transfer team and play a key role in bringing innovative chemical processes from development to full-scale GMP manufacturing.

This is an exciting opportunity for an early-career professional who is passionate about pharmaceutical manufacturing, thrives in a fast-paced technical environment, and loves collaborating across diverse scientific and operational teams.

About the Role

As a Process Specialist, you will serve as a critical bridge between our R&D teams, Operations, and our clients. Working under the guidance of senior team members, you will help design, implement, and support safe, scalable, and compliant manufacturing processes within our cGMP facilities.

This client-facing, cross-functional role offers hands-on exposure to every stage of the manufacturing lifecycle-from process design and batch record generation to on-the-floor support and production troubleshooting. It’s the perfect entry point for someone eager to grow into a technical operations, technology transfer, or manufacturing leadership path.

Duties & Responsibilities:

Be a Key Contributor to Process Scale-Up & Technology Transfer

  • Collaborate with stakeholders across R&D, QC, QA, Operations, Supply Chain, and Engineering to design safe, scalable processes from gram to multi-kilogram scale.
  • Support the generation, review, and execution of Master Batch Records (MBRs), Production Batch Records (PBRs), and Executed Batch Records (EBRs).
  • Provide technical support during manufacturing campaigns, spending required time “on the floor” to guide batch execution.

Drive Operational Readiness & Project Success

  • Participate in batch scheduling, readiness checks, material availability reviews, and daily Operations activities.
  • Support Material Readiness by coordinating bills of materials (BOMs) and maintaining tracking tools.
  • Contribute to Campaign Summary Reports and process data trending to support continuous improvement.

Serve as the Operations Point of Contact

  • Represent Operations in internal and external project meetings.
  • Provide timely production updates to clients and help maintain strong communication throughout each project.
  • Assist in managing process deviations, amendments, SOP updates, and other quality-related activities.

Contribute to a Culture of Safety & Compliance

  • Uphold cGMP, Environmental Health & Safety (EHS), Good Documentation Practices, and internal procedures.
  • Ensure accurate, timely documentation and escalate any incidents or concerns.

Participate in On-Call Support (as per rotation)

  • Provide after-hours support to resolve processing issues, report IPCs, and collaborate with QA, R&D, and Ops leadership when needed.
  • A degree in chemistry, chemical engineering, life sciences, or a related discipline.
  • Ability to work effectively in a regulated environment
  • Strong attention to detail and commitment to safety and compliance.
  • Excellent communication and collaboration skills.
  • An eagerness to learn, ask questions, and grow within a high-performing technical environment.
  • A passion for solving problems and supporting complex chemical manufacturing processes.

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.

The starting annual base compensation for this position is $65,000 CAD. The actual offer, reflecting the total compensation package plus benefits, will be determined by a number of factors which include but are not limited to the applicant’s experience, knowledge, skills, and abilities.

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

This posting is supported by AI technology to assist in screening candidates and resumes. All hiring decisions are made by human reviewers.

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

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.

NO AGENCIES, CALLS OR EMAILS PLEASE

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