
Senior Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.
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.
We are looking for an experienced and driven Senior Research Chemist to lead and execute analytical activities supporting Drug Product Development and GMP operations. In this critical role, you’ll take ownership of analytical services across the product lifecycle—contributing to innovation, quality, and regulatory compliance.
You will play a key role in method development, transfer, and phase-appropriate validation, while also supporting QC release, stability programs, and investigations. As a senior member of the team, you may also mentor or oversee junior staff, helping drive excellence across the lab.
This role is ideal for a hands-on scientific leader who thrives in a fast-paced GMP environment, with a strong focus on problem-solving, compliance, and continuous improvement.
· Lead analytical method development, transfer, and validation for oral drug products
· Support QC release testing, stability studies, and investigations (OOT/OOS/Deviations)
· Author and review GMP documentation including methods, specifications, protocols, and SOPs
· Troubleshoot and maintain analytical instruments (HPLC, GC, KF, etc.)
· Ensure compliance with cGMP, GLP, and regulatory guidelines (ICH)
· Help foster a safe, compliant, and high-performing laboratory environment
B.Sc. or M.Sc. in Chemistry with >10 years experience or Ph.D in Chemistry with >5 years experience in the pharmaceutical-related field industry
Must have a strong knowledge of drug product development and hands-on experience in analytical development
Must be highly motivated and have a proven record of success in multiple projects
Must be well organized and able to meet project timeline commitments
Must work well in a multi-disciplinary team environment and have excellent written and verbal communication skills
The starting annual base compensation for this position is $75,000 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.
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.
At Eurofins CDMO Alphora, we leverage artificial intelligence (AI) technology to support our recruitment process, including preliminary screening of applications and resumes. All hiring decisions are made by human reviewers.
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.
NO AGENCIES, CALLS OR EMAILS PLEASE
Originally posted by Eurofins. View original posting
BioCareerAI is an independent job platform and is not affiliated with or endorsed by Eurofins.
