About this role
Under the direction of Department Head of R&D, LCMSMS analyst would be responsible for supporting the department analyzing Raw Material, Bulk & Finished Products in a cGMP laboratory that meets the departmental goal.
Key Responsibilities:
Perform Method Development, Method Validation, Method Transfer and Routine Analysis using LCMSMS and other instrumentation techniques.Reviewing data, preparing protocol and report to ensure R&D projects meet the timeline;Troubleshoot technical issues/ difficulties with all tests related with Analytical Laboratory;Perform instrument calibration, qualification and preventative maintenance program as necessary;Manage multiple research projects simultaneously to meet the project timeline;Verify that all study materials (including standards, reagents and columns) are in stock;Perform investigations and troubleshoot non-confirmatory results or methods;Understand and follow Quality System documents relevant to responsibilities, e.g. Quality Manual, SOPs, GMP/GLP/USP and Methods;Adhere to appropriate quality measures to meet or exceed the standards set by GMP government regulatory and company requirements relevant to assigned duties;Maintaining a neat and accurate record system of daily activities related with all R&D and Quality Control testing;Guide, mentor and train junior staff members to achieve expected quality and TAT metrics;Any tasks as required by supervisor or Management in all aspects of business to meet the departmental goals. A minimum of 3-5 years working experience in the Pharmaceutical/Biopharmaceutical field, in a GMP environment;Strong experience with Method Development, Method Validation, Method Transfers study;Computer proficiency-MS Office (Outlook, Word, Excel), LIMS, Empower & Analyst Software in a GMP environment.HPLC-PDA & GCMSMS experience would be an asset.Education:
Bachelor of Science in Chemistry, or diploma in related field;A solid background of Mass Spectrometry is mandatory.Please note that this role will require relocation to the Company’s Mississauga office following a planned office move in 2026.
Working Conditions: This position will be working in a laboratory environment where standing is required for greater than 50% of the time to work at the bench for analyses. Light lifting requirements of up to 20 kg.
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.
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