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

Eurofins; Mississauga; On-site; CAD 70,000 - 85,000; Full time

Job summary

A leading scientific services company located in Mississauga is seeking a Research Chemist responsible for analytical method development and compliance. You will work in a GMP environment, ensuring safety and quality standards while supporting client projects. Ideal candidates possess a degree in Chemistry or Biochemistry and have experience in pharmaceutical testing and method validation.

Benefits

Health & dental coverage

Life and disability insurance

RRSP with 3% company match

Paid holidays

Paid time off

Qualifications

• 3+ years' experience in a pharmaceutical laboratory or manufacturing environment.
• 2+ years of method transfer/validation.
• Expertise in GMP, GLP and Health Canada guidelines.

Responsibilities

• Conduct work in a safe manner and ensure compliance with established safe work practices.
• Provide support for analytical activities including method development, method validation, and testing.
• Assist in the execution of prototype and GMP stability studies.

Skills

Analytical method development

Method validation

GMP compliance

GLP compliance

Education

Degree in Chemistry or Biochemistry

Job description

Overview

The Research Chemist is accountable to the Head of Pre-Formulations. Responsibilities include support for general laboratory operations, equipment on-boarding, equipment setup and operation. The Research Chemist will also participate in analytical method development, validation/transfer and testing to support the development of liquid and solid oral dosage forms.

Responsibilities

• Conduct work in a safe manner and ensure compliance with established safe work practices and procedures.
• Adhere to the policies and guidelines set out in the Eurofins CDMO Alphora Employee Handbook.
• Work harmoniously with all fellow employees.
• Provide assistance and support for analytical activities including analytical method development, method validation, method transfer, and sample testing in an R&D and GMP environment.
• Assist in the execution of prototype and GMP stability studies in accordance with ICH or other regulatory guidelines.
• Provide support for document preparation of material specifications, standard operation procedures, and other necessary documentation for Drug Product Operations.
• Ensure that all work is performed in compliance with the applicable SOPs, cGMPs and GLPs.
• Support the Drug Product Operations Team to ensure the timely completion of client projects.
• Perform other related duties as required.

Qualifications

• Degree in Chemistry, Biochemistry or related field
• 3+ years' experience in a pharmaceutical laboratory or manufacturing environment
• 2+ years of method transfer/validation
• Expertise in GMP, GLP and other Health Canada guidelines

Benefits

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.

Additional Information

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may email a request via the website. We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position.