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

Eurofins QTA Inc.

Mississauga

On-site

CAD 80,000 - 120,000

Full time

30+ days ago

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Job summary

This innovative firm is seeking a Senior Research Chemist to lead analytical services for drug product development. You will play a crucial role in method development, validation, and compliance with GMP regulations, ensuring the highest standards in pharmaceutical testing. Join a dedicated team focused on improving patient health through cutting-edge therapeutics. With a commitment to safety and excellence, this position offers a dynamic environment where your expertise will directly contribute to impactful projects. If you have a passion for chemistry and a proven track record in the pharmaceutical industry, this is an exciting opportunity to advance your career.

Benefits

Health & Dental Coverage
Life and Disability Insurance
RRSP with 3% Company Match
Paid Holidays
Paid Time Off

Qualifications

  • 10+ years in pharmaceutical-related field with strong analytical development skills.
  • Ability to draft GMP documentation and conduct stability studies.

Responsibilities

  • Oversee analytical services for Drug Product development and GMP operations.
  • Draft GMP documentation and develop analytical methods.

Skills

Analytical Development
Drug Product Development
Method Development
Troubleshooting
Team Collaboration
Communication Skills

Education

B.Sc. in Chemistry
M.Sc. in Chemistry
Ph.D. in Chemistry

Tools

HPLC
GC
KF

Job description

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

Company Overview:

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. Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients.

The Sr. Research Chemist will be responsible for overseeing and executing analytical services in support of Drug Product development and GMP operations. Primary responsibilities will include analytical services such as method transfer, method development, and phase appropriate method validation.

DUTIES AND RESPONSIBILITIES:

  • Draft GMP documentation such as test methods, material/product specifications, protocols, and SOP’s as required.
  • Develop and execute analytical methods in support of oral drug product development.
  • Conduct OOT/OOS/Deviation investigations as required.
  • Troubleshoot, maintain and perform equipment qualifications for HPLC’s, GC’s, KF and other analytical equipment as required.
  • Conduct prototype and GMP stability studies in accordance with ICH or other regulatory guidelines.
  • Ensure all work is performed in compliance with applicable SOP’s, cGMP’s, and GLP’s.
  • Promote and maintain a safe and healthy working laboratory environment in compliance with established health and safety procedures.
  • Other duties as assigned.

Minimum 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.
  • Strong knowledge of drug product development and hands-on experience in analytical development.
  • Highly motivated with a proven record of success in multiple projects.
  • Well organized and able to meet project timeline commitments.
  • Ability to work well in a multi-disciplinary team environment with excellent written and verbal communication skills.

Benefits:

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, and 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.

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.

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