Quality Control Laboratory Technician

About Jubilant Radiopharma

At Jubilant Radiopharma, we help improve patient care by producing and delivering high-quality radiopharmaceutical products. We foster a collaborative, safe, and inclusive workplace where people can learn, grow, and make a meaningful impact every day.

Role Overview

As a member of the Quality Control team, you will help ensure product quality, integrity, and compliance by performing chemical and physical testing on raw materials, intermediate products, finished products, and packaging components. You will support laboratory operations in a highly regulated environment while working closely with internal and external partners.

SHIFT: Monday to Thursday SCHEDULE: Evening –

Starting between 1:00 PM and 4:00 PM and ending between 9:00 PM and 12:00AM

Key Responsibilities

• Perform chemical and physical analyses on raw materials, intermediate products, finished products, stability samples, and packaging components.
• Follow approved analytical methods, procedures, specifications, and GMP requirements.
• Participate in method qualification, process validation, and periodic equipment qualification activities.
• Verify laboratory equipment usage logs.
• Provide technical support and assist in training team members on analytical techniques.
• Execute analytical protocols, investigations, and re-analysis activities when required.
• Conduct radioactive laboratory monitoring activities, including daily Lab Surveys and weekly Wipe Tests.
• Sample raw materials, packaging components, intermediate products, and finished products.
• Perform radiochemical purity testing on lyophilized kits.
• Ensure data integrity, traceability, and compliance of laboratory documentation.
• Coordinate testing activities with external laboratories as needed.
• Act as a resource for analytical troubleshooting and laboratory equipment support.
• Work in compliance with GMP, GLP, and HSE standards and procedures.
• Participate in investigations involving out-of-specification, out-of-trend, or other atypical laboratory results.

Qualifications

• College diploma in Analytical Chemistry, Chemistry-Biology, or Biotechnology; or a Bachelor's degree in Chemistry, Biochemistry, or equivalent with a concentration in Analytical Chemistry.
• One to two years of experience in a pharmaceutical quality control laboratory or pharmaceutical analytical testing environment.
• Strong knowledge of analytical techniques and laboratory instrumentation.
• Hands-on experience with HPLC, GC, Atomic Absorption (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.
• Strong written and verbal French communication skills.
• Written English. Technicians must use USP (United States Pharmacopeia), EP (European Pharmacopeia), or ACS (American Chemical Society) monographs, which are available only in English. Technicians must have sufficient English proficiency to understand the requirements of these monographs, apply them, and document them appropriately.