The Scientist III will apply scientific expertise to select appropriate assays for the characterization and quality control of vaccines and other products to support the manufacturing processes and develop test methods for use as release, stability, and/or characterization assays for new vaccine products. Test method development encompasses literature search, feasibility assessment, assay optimization, and qualification/validation. This position:

implements and maintains GxP compliant instruments and testing where required;
keeps informed of relevant quality, regulatory, and GxP environments and regulations;
provides scientific guidance for data interpretation, analysis and suitability of test methods;
keeps abreast of relevant technology development and assists with implementation of new technologies into the Platform with a technical focus on mass spectrometry.

Qualifications

EDUCATION

M.Sc. Degree with a minimum of 4-6 years of relevant work experience; Ph.D. in Biochemistry or related field with a minimum of 2-4 years of relevant experience preferred

KEY QUALIFICATIONS

Familiarity with testing in compliance with current regulations is preferred
Experience in the following:
- Intact protein MS
- HDX-MS
- Peptide based workflows
- LC-MS small molecule and peptide quantification
- Chromatographic separation techniques such as RPLC and HILIC
- Glycoproteomics
- Lipidomics and metabolomics are assets

Specific experience in the development of liquid chromatography - mass spectrometry workflows (LC-MS) for biomolecules/vaccines and process impurities
Familiarity with a broad range of protein/peptide/biomolecule workflows and mass spectrometry instrumentation including nano chromatography and/or analytical chromatography applications
Experience with QTOF, Orbitrap or triple quadrupole MS systems
Experience in maintaining laboratories and equipment in cGMP and/or GLP compliance.
Proven verbal and written communication, organizational and team skills are required

WORKING CONDITIONS

This position will be working in a laboratory environment where most of the time will be standing or sitting at a lab bench, or sitting at a desk working on a computer. Light-intermediate lifting requirements of no more than 30 lbs. Hazardous materials are handled using established safety procedures and appropriate PPE.
Shift work and extra hours may be required, as well as working periodic weekends and/or evenings.

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.

This posting is for a current vacancy and the successful candidate will start as soon as possible.

Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process.

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