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Job summary

Perform analytical testing for pharmaceutical product development, including HPLC, sample preparation, titration, dissolution and stability testing, physical characterization, and OOS investigations. Document and evaluate results against R&D and GMP criteria, follow laboratory safety procedures and SOPs, maintain laboratory supplies and organization, and support analytical investigations.

Job details

Tasks and Responsibilities Perform Analyses Related To Pharmaceutical Product Development Activities Using a Variety Of Analytical Techniques And Laboratory Instrumentation. This Includes, But Is Not Limited To High Performance Liquid Chromatography (HPLC) Sample preparation Titration Dissolution testing Stability testing Physical characterization of APIs, intermediates, and finished products Out-of-Specification (OOS) investigations The Successful Candidate Will Also Adhere to laboratory health, safety, and hygiene procedures; Demonstrate proficiency in analytical methods, laboratory techniques, and the operation of analytical instruments; Meet established timelines and priorities; Maintain accurate and up-to-date documentation related to laboratory activities; Comply with Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP); Actively participate in analytical investigations as required; Monitor and maintain inventories of reagents, reference standards, and chromatographic columns; Ensure the general upkeep and organization of the laboratory; Perform analyses according to approved procedures, accurately document results in laboratory reports, and evaluate data against R&D and GMP acceptance criteria under the guidance of the supervisor; Perform other related duties as assigned. Qualifications Diploma of Collegial Studies (DEC) in Chemistry, Biochemistry, Laboratory Technology, Pharmaceutical Sciences, or a related field; Minimum of 3 years of experience in a related laboratory environment; Bilingual (English and French); Proficient in Microsoft Office 365. Job Type Full-time, Permanent Salary Starting at $50,000 per year Benefits Dental insurance Extended health care Life insurance Paid time off Employer-matched Registered Retirement Savings Plan (RRSP) Location Requirements Commute or Relocation Must be able to reliably commute to Laval, Québec, or relocate before starting employment (required). Education Diploma of Collegial Studies (DEC) (preferred) Experience Laboratory experience: 3 years (preferred) Work Location On-site

What you’ll do

Perform analytical testing for pharmaceutical product development, including HPLC, sample preparation, titration, dissolution and stability testing, physical characterization, and OOS investigations. Document and evaluate results against R&D and GMP criteria, follow laboratory safety procedures and SOPs, maintain laboratory supplies and organization, and support analytical investigations.

Requirements

A DEC in Chemistry, Biochemistry, Laboratory Technology, Pharmaceutical Sciences, or a related field is preferred, along with at least three years of related laboratory experience. The candidate must be bilingual in English and French and proficient in Microsoft Office 365.

Benefits

• Dental Insurance
• Extended Health Care
• Life Insurance
• Paid Time Off
• Employer-Matched Registered Retirement Savings Plan (RRSP)

Listed skills

• Inventory management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• High-Performance Liquid Chromatography (HPLC)
• Sample Preparation
• Titration
• Dissolution Testing
• Stability Testing
• Physical Characterization
• Out-of-Specification (OOS) Investigations
• Analytical Methods
• Laboratory Instrumentation
• Laboratory Documentation
• Good Manufacturing Practices (GMP)
• Standard Operating Procedures (SOPs)
• Data Evaluation
• Inventory Management
• Microsoft Office 365

Job areas

• Science & Research
• Manufacturing
• Healthcare