Production Technician

Jubilant Radiopharma; Kirkland; Presencial; CAD 45.000 - 75.000; Jornada completa

Descripción de la vacante

Jubilant Radiopharma is hiring a Production Technician to support radiopharmaceutical manufacturing in a highly regulated setting. You will ensure aseptic processing, comply with quality and radiation safety standards, and support daily production activities.

Key duties include preparing materials, verifying batch records, performing in-process tests, and maintaining strict documentation per ALCOA+ principles. Strong attention to detail and teamwork are essential.

Formación

• Education in a relevant field (AEC/DEC/Bachelor or equivalent).
• Experience in pharma/GMP-regulated environment is an asset.
• Aseptic environment and cleanroom procedures are an asset.
• Ability to learn and follow detailed procedures under strict quality/regulatory requirements.
• Proficiency with MS Word and Excel.
• Excellent French written and verbal communication.

Responsabilidades

• Perform manufacturing operations for radiopharmaceutical products in line with procedures.
• Carry out production activities in classified environments with aseptic requirements.
• Gowning in aseptic areas and maintaining cleanroom practices.
• Follow gowning procedures for Grade C and Grade D areas.
• Prepare solutions, materials, and equipment for production tasks.
• Review and execute batch records and work orders accurately.
• Document production activities in real time per ALCOA+.
• Conduct in-process tests and verifications.
• Handle radioactive sources following radiation safety procedures.
• Perform environmental monitoring, including swipe tests and contamination checks.
• Maintenance, calibration, and cleaning as required.
• Manage radioactive waste safely per procedures.
• Complete SAP transactions and assist with inventory management.
• Document Deviations, incidents, and out-of-spec conditions.
• Contribute to continuous improvement and training of new staff.

Conocimientos

Aseptic processing

Quality compliance

Radiation safety

ALCOA+ documentation

Batch records

MS Word/Excel

French communication

Attention to detail

Teamwork

Educación

AEC/DEC/Bachelor equivalent in relevant field

Herramientas

SAP

Descripción del empleo

Career Opportunities: Production Technician (1996)

At Jubilant Radiopharma, we help support patient care through the manufacturing of radiopharmaceutical products used in healthcare. Our success is built on dedicated people who value quality, safety, teamwork, and continuous improvement.

Role Overview

As a Production Technician, you will play an important role in the manufacturing of radiopharmaceutical products within a highly regulated environment. You will help ensure compliance with quality, aseptic processing, and radiation safety standards while supporting daily production activities.

Key Responsibilities

• Perform manufacturing operations for injectable and oral radiopharmaceutical products in accordance with established procedures.
• Carry out production activities in classified environments while complying with current aseptic requirements.
• Perform aseptic gowning according to procedures and maintain proper cleanroom practices.
• Follow gowning procedures for classified areas (Grade C and Grade D).
• Prepare solutions, raw materials, and equipment required for production activities.
• Review and execute batch records and production work orders accurately.
• Complete production documentation in real time in compliance with ALCOA+ principles.
• Conduct in-process tests, measurements, and verification activities.
• Handle radioactive sources, including iodine and strontium, in strict compliance with radiation safety procedures.
• Perform environmental monitoring activities, including swipe testing and contamination monitoring.
• Perform cleaning, disinfection, verification, maintenance, and calibration activities as required.
• Ensure the safe management and disposal of radioactive waste according to internal procedures.
• Complete required transactions in computerized systems, including SAP.
• Participate in inventory activities and material management.
• Identify, document, and report deviations, incidents, and out-of-specification conditions.
• Contribute to continuous improvement initiatives and documentation updates.
• Collaborate with team members and support the onboarding and training of new employees.

Qualifications

• Completed AEC, DEC, Bachelor's degree, or equivalent education in a relevant field.
• Experience in a pharmaceutical, biotechnology, or GMP-regulated environment is an asset.
• Ability to work in an aseptic environment (classified areas, sterile gowning) and follow strict cleanroom requirements is an asset.
• Demonstrated ability to learn and apply detailed procedures while complying with strict quality and regulatory requirements.
• Basic proficiency in Microsoft Word and Excel.
• Excellent French communication skills, both written and verbal.
• Strong manual dexterity and ability to maintain sustained concentration.
• Strong communication skills and attention to detail.
• Ability to work effectively in a fast-paced team environment.