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, and
- Continuous Training and skill development
POSITION TITLE: Laboratory Analyst Level 1
REPORTS TO: Director of Laboratory Operation
POSITION SUMMARY:
This is a lab-based position and will assist the QC Supervisor and Technical Department with various QC functions on daily basis for the successful and smooth functioning of the QC unit as a whole.
The Quality Control Chemist is responsible to perform all phases of chemical testing of raw material, in-process, and finished product control samples and performing analytical testing following the written procedure or compendial methods (i.e., USP, EP, BP, etc.) under supervision and instruction; Prepare analytical equipment for experiments, including reagents, standards, test solutions, and mobile phase as required by the test procedure. Receive, organize and distribute samples according to the procedures; document testing results appropriately ensuring the data meets the specifications. Operate, maintain, and perform basic troubleshooting of analytical instruments, including; Dissolution, HPLC, UV-VIS, TOC, KF, IR, Potentiometer, LOD, Titration, etc.
ESSENTIAL FUNCTIONS
- Perform raw material, in-process, finished product, and stability sample testing using instrumental analytical, wet chemicals, 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
- Ordering general lab supplies (chemicals/non-chemicals) when required.
- Document testing results in lab notebooks; 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 lab-books, equipment logbooks, and trackers on daily basis in accordance with department policies and procedures.
- Send out raw materials and finished products as per company policy and procedures.
- Effectively manage the prioritization to meet multiple goals and timelines.
- Conduct laboratory housecleaning and upkeep, maintain and promote 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 new or existing personnel as identified by QC management.
- Notify any aberrant/OOS/OOT results to QC management and participate to investigate results following the SOP.
POSITION 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 area
- Minimum B.Sc. in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 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, etc.
- Well versed in understanding USP, BP, EP, and JP, methods and specifications.
- In-depth knowledge and competency in cGMP/GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), 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.
HOW TO APPLY
Please reference “Laboratory Analyst Level 1” in subject line and submit resume with cover letter to [email protected]
We welcome and encourage applications from all qualified applicants. We are committed to adhering to our company objectives and requirements outlined above. Kindly refrain from applying if you are not qualified.
We thank all applicants for their interest, however, only those qualified and selected shall be contacted for an interview.
No phone calls please.
Pay: $40,000.00-$50,000.00 per year
Benefits:
- Dental care
- Life insurance
- On-site parking
- Vision care
Application question(s):
- Minimum B.Sc. in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 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, etc.
- Well versed in understanding USP, BP, EP, and JP, methods and specifications.
- In-depth knowledge and competency in cGMP/GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), GXP, FDA CFR 211, ICH, and ALCOLA+ regulation and quality system guidelines.
Work Location: In person
