Laboratory Analyst Level 1 (Markham)

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 misuse. We are an equal-opportunity employer committed to diversity and inclusion for everyone. We continuously look for smart-mindded, 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, and Continuous Training and skill development. Position Summary

This is a lab-based position that assists the QC Supervisor and Technical Department with various QC functions on a daily basis for the successful and smooth functioning of the QC unit as a whole. Essential Functions

Perform raw material, in-process, finished product, and stability sample testing using instrumental analytical, wet chemistry, and physical analytical methods and techniques following the written procedure or compendial methods. Prepare analytical equipment for experiments, including reagents, standards, test solutions, and mobile phase as required by the test procedure. Maintain accurate documentation, including lab reports, records of procedures, results, and data analysis in accordance with Good Documentation Practices (GDP) guidelines. Order general lab supplies (chemicals/non-chemicals) when required. Document testing results in lab notebooks and ensure the data generated is accurate and meets the specifications. Report results on the testing worksheets (finished products and raw materials) according to standard operating procedures in a timely manner, meeting specified deadlines. Maintain laboratory logbooks, equipment logbooks, and trackers on a daily basis in accordance with department policies and procedures. Send out raw materials and finished products as per company policy and procedures. Effectively manage prioritization to meet multiple goals and timelines. Conduct laboratory house-cleaning and upkeep, maintaining a safe and orderly work area. Participate in laboratory overall improvement and other work/duties as assigned, as well as other miscellaneous duties as required. Adhere to established company procedures, cGMP, cGLP, Health Canada, FDA, ICH, and other regulatory regulations. Provide guidance and training to new or existing personnel as identified by QC management. Notify QC management of any aberrant/OOS/OOT results and participate in investigating results following the SOP. Position Requirements

Must possess permanent Canadian residency with work permit and/or Canadian citizenship. Must be living in Canada, preferably in the Toronto area. Minimum B.Sc. in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least 2 years hands-on experience working in pharmaceutical and/or allied industries. Solid knowledge and expertise (including operation, qualification, trouble-shooting, and maintenance) working with laboratory instrumentation such as dissolution, HPLC, UV-VIS, TOC, KF, IR, potentiometer, and others. Well versed in understanding USP, BP, EP, and JP, methods and specifications. In-depth knowledge and competency in cGMP/GMP, GDP, GXP, FDA CFR 211, ICH, and ALCOLA+ regulation and quality system guidelines. Strong attention to detail. Strong problem-solving and analytical skills including decision analysis and implementation. Computer proficiency with MS Office (Excel, Word, PowerPoint), spreadsheets, etc. Strong ability to function as a team member; ability to communicate effectively with team members and other plant personnel, both verbally and in writing. Track record of multi-tasking, being detail-oriented, trouble-shooting/problem-solving abilities, working in a fast-paced environment with minimal instruction on routine work and moderate instruction on new assignments. Be punctual, team player, fast learner, and have strong interpersonal and communication skills. Equal Opportunity Statement

We are an equal-opportunity employer committed to diversity and inclusion for everyone.

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