Analytical Laboratory Technician
- Laval, QC, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Experience
- Minimum of 3 years of experience in a related laboratory environment;
- Posting language
- English
- Posted
Original job description
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
Full-time, Permanent
Salary
Starting at $50,000 per year
Benefits
Commute or Relocation
On-site
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
- 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.
- 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.
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)
Commute or Relocation
- Must be able to reliably commute to Laval, Québec, or relocate before starting employment (required).
- Diploma of Collegial Studies (DEC) (preferred)
- Laboratory experience: 3 years (preferred)
On-site
More about this job
Responsibilities
Conduct 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 procedures and safety requirements, maintain supplies and equipment, and support laboratory organization and 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.
Skills
- 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
- Microsoft Office 365
- Laboratory Safety
- Inventory Management
Benefits
- Dental Insurance
- Extended Health Care
- Life Insurance
- Paid Time Off
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Manufacturing
- Healthcare
Keywords
- Pharmaceutical Product Development
- Analytical Testing
- Sample Preparation
- Titration
- Dissolution Testing
- Stability Testing
- Physical Characterization
- Active Pharmaceutical Ingredients (APIs)
- Intermediates
- Finished Products
- Out-of-Specification (OOS) Investigations
- Analytical Methods
- Laboratory Instrumentation
- Good Manufacturing Practices (GMP)
- Standard Operating Procedures (SOPs)
- R&D Acceptance Criteria
- Laboratory Reports
- Reagents
- Reference Standards
- Chromatographic Columns
- Microsoft Office 365
- Laboratory Safety
- Inventory Management
- Pharmaceutical Manufacturing