Scientist Analytical Development- Eurofins CDMO Alphora Inc

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/latestage method development/testing within the Biologics Business Unit to meet the business objectives.

Duties and Responsibilities:

• 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.

Qualifications :

• PhD in chemistry Biochemistry or biological sciencewith 3 years of relevant industry experience and quality control experience or Masters degree in chemistry Biochemistry or biological science with 5 years of relevant industry experience and quality control experience
• Broad understanding of stateoftheart physicochemical analyses and ability to design comprehensive biologics characterization strategy.
• Proficient to HPLC CE and/or bioassay
• Handson experience with Empower 3
• Having extensive handson 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.
• Indepth understanding of analytical development strategy to support regulatory filing.
• Being proactive and flexible

Additional Information :

At Eurofins we offer excellent fulltime 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 email a request via the website at 

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 

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.

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Remote Work :

No

Employment Type :

Fulltime