Sr. Lab Analyst, LC-MS / MS Operator

Pharma Medica Research Inc.; Ontario; On-site; CAD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a skilled Sr. Lab Analyst to support bioanalytical drug testing and analysis. This role involves ensuring the calibration and maintenance of essential laboratory equipment, coordinating supplies for clinical studies, and supervising technicians. The ideal candidate will possess a strong background in chemical technology, excellent communication skills, and the ability to work both independently and collaboratively. Join a dynamic team dedicated to conducting high-quality research and contributing to the advancement of clinical trials in a supportive environment.

Qualifications

• 1-2 years of bioanalytical technician experience required.
• Proficient in English with strong communication skills.

Responsibilities

• Ensure calibration and operation of laboratory equipment.
• Supervise technicians and maintain accurate records.

Skills

Bioanalytical Testing

HPLC

LC/MS

GLP Compliance

Communication Skills

Education

B.Sc. in Chemical Technology

Community College Diploma in Related Science

Tools

HPLC Equipment

LC-MS/MS Equipment

Laboratory Balances

Pipettes

Job description

Pharma Medica Research is a full-service contract research organization specializing in conducting early-phase clinical trials in healthy volunteers, as well as in special and patient populations. We are currently seeking a Sr. Lab Analyst to join our team!

Position Overview

The Sr. Bioanalytical Analyst primarily supports bioanalytical drug testing and analysis. This position reports to the Team Leader / Bioanalytical Lab and/or designate.

Duties and Responsibilities

1. Ensure calibration, maintenance, and operation of all principal laboratory equipment, including HPLC, LC/MS, LC-MS/MS (training will be provided if not experienced), balances, pH meters, pipettes, freezers, water systems, and equipment for sample extraction, evaporation, and fume hoods.
2. Coordinate supplies and preparations for assigned clinical or pre-clinical studies, including ordering supplies, preparing pools and randomization charts, and training technicians in analytical methods.
3. Supervise technicians during sample preparation and approve documentation.
4. Write and update Standard Operating Procedures (SOPs) as required.
5. Perform method validations and prepare method reports.
6. Coordinate with Principal Bioanalytical Investigator and Quality Control to ensure timely completion of analytical assays.
7. Maintain accurate records and logs in compliance with GLP/SOPs and regulatory requirements.
8. Conduct laboratory activities in accordance with PMRI's SOPs and Good Laboratory Practices (GLPs).
9. Attend SOP and GLP training sessions; contribute suggestions for operational improvements and SOP content.
10. Assist in the development and validation of bioanalytical methods in line with FDA, TPP, and other international standards.
11. Perform other duties as assigned.

Qualifications

• B.Sc. or Community College diploma in Chemical Technology or a related science.
• 1-2 years of related bioanalytical technician experience.
• Proficient in English, with good verbal and written communication skills.
• Strong interpersonal skills.
• Ability to work independently and as part of a team.