IN 2024, 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 Scientist in Analytical Development is responsible for being a team lead in the development of analytical development for biologics and therapeutics by assuming crucial role in the design and execution of a complete analytical testing. The scientist is accountable to the Manager, Analytical Development in Biologics to execute/report on analytical development activities, including technology transfer, planning and execution of technology/method transfer, early/late-stage method development/testing within the Biologics Business Unit to meet the business objectives.

QUALIFICATIONS

• PhD in chemistry, Biochemistry, or biological sciencewith 3 + years of relevant industry experience and quality control experience or Master’s degree in chemistry, Biochemistry, or biological science with 5 + years of relevant industry experience and quality control experience
• Broad understanding of state-of-the-art physico-chemical analyses and ability to design comprehensive, biologics characterization strategy.
• Proficient to HPLC, CE and/or bioassay
• Hands-on experience with Empower 3
• Having extensive hands-on experience with multiple biophysical technologies for the characterization of higher order structure of biologics is an asset.
• Practical understanding of biologics purification process is an asset.
• Outstanding written and verbal communication skills, with the ability to convey strategies and results to a diverse audience.
• In-depth understanding of analytical development strategy to support regulatory filing.
• Being proactive and flexible
  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.
  This posting is supported by AI technology to assist in screening candidates and resumes.

• Comprehensive understanding of testing with analytical instrument, bioprocessing, and industrial biotechnology
• Experience and good understanding of aseptic techniques in laboratory setting
• Basic understanding of how to implement Design of Experiments (DoE) and Quality by Design (QbD) in biopharmaceutical industry.
• Good understanding of Current Good Manufacturing Practices (cGMP) in biomanufacturing
• Leading projects, scientific communication, dealing with clients, etc.
• Strong documentation and technical writing skills, and able to apply relevant scientific principles and practices.
• Strong command over written and verbal English
• Able to work under minimal supervision and able to work independently and in a team environment.
• Able to exercise appropriate professional judgement on matters of significance.
• Proficient in computer skills and software applications such as MS tools
• Knowledge of statistical packages
• Must communicate clearly and concisely across levels, both orally and in written
• Proven ability to effectively and independently design and plan experiments, prioritize tasks and critically evaluate results under compressed timelines.