About Jubilant Radiopharma

At Jubilant Radiopharma, we are committed to delivering high-quality radiopharmaceutical products that support healthcare professionals and patients across North America. We value collaboration, innovation, integrity, and excellence in everything we do.

We are currently seeking Quality Control Laboratory Technicians to join our team in Kirkland, Quebec.

Role Overview

As a Quality Control Laboratory Technician, you will support testing and quality activities that ensure the safety, quality, compliance, and integrity of pharmaceutical products. This role is ideal for someone who enjoys working in a highly regulated environment where accuracy, attention to detail, and continuous learning are essential.

SHIFT: Monday to Friday

SCHEDULE: Evening – Starting between 1:00 PM and 4:00 PM and ending between 9:00 PM and 12:00 AM.

Key Responsibilities

• Perform chemical and physical analyses on finished products, intermediates, raw materials, packaging components, stability samples, and validation samples.
• Conduct testing in accordance with approved methods, procedures, specifications, and Good Manufacturing Practices (GMP).
• Participate in method qualification activities, in-process testing, and equipment calibration, verification, and maintenance activities.
• Review laboratory equipment usage logs.
• Provide technical support related to analytical methods when required.
• Support the training of new and existing team members on analytical techniques.
• Execute analytical protocols, including re-analysis and investigation-related activities.
• Conduct daily radioactive laboratory contamination monitoring (Lab Survey) and weekly Wipe Tests.
• Perform sampling of raw materials, packaging components, intermediates, and finished products.
• Verify labels and product components.
• Coordinate testing activities with external laboratories as required.
• Perform radiochemical purity testing on lyophilized kits.
• Maintain complete, accurate, and compliant laboratory documentation.
• Ensure data integrity, traceability, and accuracy of all generated and reported results.
• Act as a resource for analytical issues and laboratory instrument support.
• Perform work in accordance with GMP, GLP, and HSE policies and procedures.
• Maintain clean and organized work areas.
• Promptly report out-of-specification results, deviations, incomplete analyses, or any irregularities and participate in investigations.
• Perform other related laboratory and quality control duties as assigned.

Qualifications

• College diploma in Analytical Chemistry, Chemistry-Biology, or Biotechnology; or a Bachelor's degree in Chemistry, Biochemistry, or an equivalent field.
• For university graduates, a concentration in analytical chemistry is required, including analytical techniques and instrumental analysis methods.
• One to two years of experience in a pharmaceutical quality control laboratory or pharmaceutical analytical laboratory.
• Strong knowledge of analytical techniques and laboratory instrumentation.
• Hands-on experience with HPLC, GC, AA, spectrophotometry, infrared analysis, and wet chemistry techniques.
• Knowledge of Good Manufacturing Practices (GMP) and pharmacopoeias (USP, Ph. Eur., and BP) and their application within a laboratory environment.
• Proficiency with Microsoft Office, SAP, and electronic data acquisition systems.
• Spoken and written French.
• Written English. Technicians must use monographs in their work, specifically USP (United States Pharmacopoeia), EP (European Pharmacopoeia), or ACS (American Chemical Society) monographs. These monographs are published online and are available in English only. Technicians must have sufficient English proficiency to understand the requirements of these monographs, apply them, and document them in their work tools.