Overview

About Shields Pharma Inc.Shields Pharma Inc. is a Health Canada approved GMP organization located in Markham, Ontario.We offer Laboratory R&D and QC testing services as well as production and formulation of certain psychedelic therapeutics for treatment of certain mental health disorders such as anxiety, depression, obsessive-compulsive disorder, PTSD, and problematic substance.Shields Pharma Inc. is an equal opportunity employer committed to diversity and inclusion for everyone. We are continuously looking for smart-minded, skilled, qualified, experienced, independent, reliable, and detail-oriented candidates to join our successful team.Our people are at the heart of everything we do.You can count on;Safety as our first core value,Integrity,Accountability, andContinuous Training and skill development.Position Title: Pharmaceutical Senior Laboratory Analyst IIIReports To: Chief Scientific Officer and Laboratory ManagerJob Description:The Pharmaceutical Senior Laboratory Analyst III shall support both R&D and Quality Control analytical activities at Shields Pharma laboratory.The Pharmaceutical Senior Laboratory Analyst III responsible for conducting method development and validation, method transfer, assay and impurity analysis by utilizing HPLC, LC/MS, GC-Headspace, GC/MS, and ICP-MS, projects according to the schedule established by following the procedures and adhering to Good Manufacturing Practices (GMP), GXP, and good laboratory practices.The successful candidate will be working in a very fast paced environment, performing both R&D and QC analysis of assigned raw materials, in-process, and final products as per established methods, current pharmacopoeias (e.g. USP, BP, EP, etc.), and the clients methods and specifications within standard time-lines, and under minimal guidance/supervision.This position relies heavily on comprehensive wet chemistry and strong chromatographic skills and competencies.Duties shall include but are not limited to the following:Perform all works in accordance with all established company policies, protocols and procedures, and governing regulatory, GMP compliance, and safety guidelines.Perform assay and impurities method development, method validation, method transfer, cleaning validation, and stability testing.Maintain accurate documentation including lab reports, records of procedures, results, and data analysis in accordance with Good Documentation Practices (GDP) guidelinesProvide scientific advice and training to junior analysts on laboratory instrumentation and methods.Perform peer review of analytical reports and data when requested.Document and report results in accordance with GMP and GLPConduct Laboratory Investigation (OOS, OOT, Deviation, etc.).Provide technical support to other analysts when requiredCollaborate with cross-functional teams to support R&D projects.Ensure all general lab supplies (chemicals/non-chemicals) are available at all time.Participate in client audits and health authorities regulatory inspection (i.e., Health Canada and FDA GMP, inspections, and Health Canada OCS audits).Ensure all analytical documentation including lab reports, records of procedures, results, and data analysis are accurate and in accordance with Good Documentation Practices (GDP) guidelines.Provide oversight of external vendors who are delegated responsibilities when requested.Ensure all generated documentation including lab reports, records of procedures, results, and data analysis are accurate and correct.Perform any other tasks/duties as assigned by departmental management.Job Requirements: (Work Status, Qualification, Knowledge, and Experience)Must possess Permanent Canadian residency with work permit and/or Canadian citizenship.Must be living in Canada, preferably in Toronto areaMinimum M.Sc. (min. 3 yrs. industry experience), or B.Sc. (min. 5 yrs. industry experience), preferably in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines.Must have worked