Quality Control Analytical Chemist I - Eurofins CDMO Alphora, Inc.

- Full-time
- Compensation: CAD 58,000 - CAD 58,000 - 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.

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 is looking for a dynamic Quality Control Analytical Chemist to join our Team The ideal candidate will:

- possess a high degree of initiative
- is a team player with excellent communication abilities
- is comfortable in a modern, state of the art laboratory
- has practical experience with HPLC, GC,



KF and various wet chemistry techniques
- has a strong attention to detail and a comprehensive understanding of cGMP
- has strong organizational skills with the ability to multitask and work in a rapid-paced setting

Our Quality Control department plays a key role in ensuring Eurofins CDMO Alphora Inc.'s compliance with Current Good Manufacturing Practices (cGMP) to ensure the production of safe and efficacious pharmaceutical APIs on behalf of our clients and their patients. The Quality Department is responsible for providing analytical support for the API manufacturing plant including support of raw material and finished product release, in process control testing, cleaning verification and other investigations.

You will be working collaboratively with a small, dedicated team of QC chemists. Teamwork, communication and individual responsibility are key requirements. This is an excellent opportunity to obtain experience in a pharmaceutical manufacturing setting and to work on projects related to all phases of the pharmaceutical product life cycle.

Responsibilities include but are not limited to:

- Testing of raw materials, in process controls, intermediates and finished products in support of our cGMP manufacturing operations.
- Interpret and report all test results, tabulate data and generate reports as required.
- Responsible to identify OOS results and assist in their investigation.
- Assist in maintaining the lab in a state of compliance by performing calibration checks and performance verifications of laboratory equipment.
- Work in accordance with established cGMP and safety requirements.
- Perform other related duties as required.

Instrumentation:

📌 Quality Control Analytical Chemist I (Oakville)
🏢 Eurofins Group
📍 Oakville