Back to job search
Eurofins Viracor logo
Eurofins ViracorVerified Job Source

Senior Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.

  • Mississauga, ON
  • On-site
  • Posted Sep 24, 2026
  • 1 position

$75,000 / year

Opens an external site

Sign in to save this job
Employment type
Full-time
Experience level
Lead · 10+ years
Minimum education
Bachelor’s degree
Posting language
English
Working hours
40 hours per week

Job summary

The Senior Research Chemist will lead analytical method development, transfer, and validation activities to support drug product development and GMP operations. They are also responsible for overseeing QC release testing, stability programs, and ensuring full regulatory compliance within the laboratory.

Job details

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 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. 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. Job Description 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. Key Highlights: · 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 · Potential to supervise or mentor team members Qualifications 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. This posting is for a talent pool to support future hiring needs and does not correspond to an existing vacancy. Additional Information 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 Compensation: CAD 75000 - CAD 75000 - yearly

What you’ll do

The Senior Research Chemist will lead analytical method development, transfer, and validation activities to support drug product development and GMP operations. They are also responsible for overseeing QC release testing, stability programs, and ensuring full regulatory compliance within the laboratory.

Requirements

Candidates must hold a B.Sc. or M.Sc. in Chemistry with over 10 years of experience, or a Ph.D. with over 5 years of pharmaceutical industry experience. Strong expertise in analytical development and a proven track record in a GMP environment are essential.

Benefits

  • Health coverage
  • Dental coverage
  • Life insurance
  • Disability insurance
  • RRSP with 3% company match
  • Paid holidays
  • Paid time off

Listed skills

  • Regulatory Compliance · Preferred
  • Troubleshooting · Preferred
  • Project management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

  • Analytical method development
  • Method validation
  • GMP documentation
  • HPLC
  • GC
  • KF
  • Drug product development
  • QC release testing
  • Stability studies
  • Regulatory compliance
  • ICH guidelines
  • Troubleshooting
  • Laboratory management
  • Mentoring
  • Project management
  • Active Pharmaceutical Ingredients
  • Good Laboratory Practice (GLP)
  • Analytical Testing
  • Method Development
  • Time Off Management
  • Analytical Method
  • Self-Motivation
  • Research
  • Application Programming Interface (API)
  • Artificial Intelligence
  • Scientific Instruments
  • Chemistry
  • Biotechnology
  • Biological Materials
  • Good Manufacturing Practices
  • Clinical Trials
  • Regulatory Compliance
  • Continuous Improvement Process
  • Genomics
  • Leadership
  • High-Performance Liquid Chromatography
  • Innovation
  • Problem Solving
  • Life Sciences
  • New Product Development
  • Operations
  • Pharmaceuticals
  • Troubleshooting (Problem Solving)
  • Verbal Communication Skills
  • Stocks (Inventory)
  • Investigation

Job areas

  • Science & Research
  • Healthcare
  • Manufacturing
  • Research Chemist
  • Research and Development Chemist
  • Chemists

More jobs from Eurofins Viracor

See all jobs from Eurofins Viracor