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

at  Eurofins Canada BioPharma

IN 2023, EUROFINS GENERATED TOTAL REVENUES OF EUR 6.515 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
The Research Chemist is accountable to the Head of Pre-Formulations. Responsibilities include support for general laboratory operations, equipment on-boarding, equipment set up 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.

DESIRED MINIMUM 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
  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.

• 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