Purpose The analytical chemist will be a key member of the R&D team who will be responsible for Analytical method development activities. This role will require method development, document preparation and other activities as required in a timely manner as per organization needs.
Position / Job Title Analytical Chemist II
Department AD – R&D
Reporting To R&D Head
Location Concord - Canada
Years of Experience 5 years related experience
Dosage Form Solid/Nasal / Liquid

Job Responsibilities / Deliverables * Provide updates and technical input to Technical Project Team for programs

• Perform routine and non-routine HPLC/GC testing and analysis on pharmaceutical products and raw materials
• Develop and validate HPLC, GC and product performance test methods for pharmaceutical products
• Prepare documents and reports necessary for development and GMP activities
• Develop specifications for finished product, bulk product, raw materials and packaging components
• Perform analytical method development and method validation for new pharmaceutical products
• Perform HPLC testing for the release of bulk and placebo formulations and for finished product
• Perform physical/comparative testing on generic and innovator products
• Conduct testing of stability and developmental stability samples
• Evaluate all results generated for consistency and accuracy and notify manager of any trends, atypical results or out-of-specification results
• Perform troubleshooting and problem solving of analytical instrumentation
• Ensure that work is performed in compliance with GMP, GLP, SOPs, and current test methods.
• Perform QMS investigations for lab activities
• Any other duties as assigned

Qualifications & Pre-Requisites

• B.Sc. degree or equivalent in an applicable discipline of science (pharmaceutical sciences, chemistry, biochemistry, chemical engineering, medical laboratory science or related)
• At least 5 years of experience in a pharmaceutical R&D laboratory and / or CMO setting
• Analytical skills required to handle complex products
• Experience in development of nasal products will be an asset
• Great attitude and motivated to learn new skills
• Good written and oral communication skills
• Ability to work independently with minimum supervision

Additional notes Role may be required to work in afternoon shift (12 pm to 8 pm) on a need basis.
Job Types: Full-time, Fixed term contract
Contract length: 12 months
Pay: $59,530.01-$70,000.00 per year

Benefits:

• Dental care
• Extended health care
• Life insurance
• On-site parking
• Paid time off

Work Location: In perso

• Perform routine and non-routine HPLC/GC testing and analysis on pharmaceutical products and raw materials
• Develop and validate HPLC, GC and product performance test methods for pharmaceutical products
• Prepare documents and reports necessary for development and GMP activities
• Develop specifications for finished product, bulk product, raw materials and packaging components
• Perform analytical method development and method validation for new pharmaceutical products
• Perform HPLC testing for the release of bulk and placebo formulations and for finished product
• Perform physical/comparative testing on generic and innovator products
• Conduct testing of stability and developmental stability samples
• Evaluate all results generated for consistency and accuracy and notify manager of any trends, atypical results or out-of-specification results
• Perform troubleshooting and problem solving of analytical instrumentation
• Ensure that work is performed in compliance with GMP, GLP, SOPs, and current test methods.
• Perform QMS investigations for lab activities
• Any other duties as assigne