Production Technician
- Greater Montreal Metropolitan Area, QC, Canada
Full-time
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Job details
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- Full-time
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- English
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Original job description
Job Description
Job Title: Production Technician
Req Id: 1996
Posting Start Date: 11/3/26
Job Description:
About Jubilant Radiopharma
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
Job Title: Production Technician
Req Id: 1996
Posting Start Date: 11/3/26
Job Description:
About Jubilant Radiopharma
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.
- 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.
More about this job
Responsibilities
Manufacture injectable and oral radiopharmaceutical products by preparing materials and equipment, executing production records, conducting in-process checks, and following aseptic and radiation safety procedures. Perform environmental monitoring, equipment and cleanroom upkeep, radioactive waste handling, inventory and SAP transactions, and report deviations while supporting continuous improvement and team training.
Requirements
A completed AEC, DEC, bachelor's degree, or equivalent education in a relevant field is required; experience in pharmaceutical, biotechnology, or GMP-regulated settings and aseptic cleanroom work is an asset. Candidates should be able to follow detailed procedures, use Microsoft Word and Excel, communicate excellently in French, and demonstrate manual dexterity, sustained concentration, attention to detail, and teamwork.
Skills
- Aseptic Processing
- Cleanroom Practices
- Radiation Safety
- Radiopharmaceutical Manufacturing
- Batch Record Documentation
- ALCOA+ Documentation
- In-Process Testing
- Environmental Monitoring
- Contamination Monitoring
- Cleaning and Disinfection
- Equipment Calibration
- Radioactive Waste Management
- SAP
- Inventory Management
- Deviation Reporting
- Microsoft Word
Visa sponsorship
Not detected in the job text
Categories
- Manufacturing
- Healthcare
- Science & Research
- Security & Safety
Keywords
- Radiopharmaceuticals
- Pharmaceutical Manufacturing
- GMP
- Aseptic Processing
- Classified Environments
- Grade C
- Grade D
- Sterile Gowning
- Cleanroom Practices
- Radiation Safety
- Iodine
- Strontium
- Batch Records
- Production Work Orders
- ALCOA+
- In-Process Testing
- Environmental Monitoring
- Swipe Testing
- Contamination Monitoring
- Cleaning
- Disinfection
- Equipment Calibration
- Radioactive Waste
- SAP
- Inventory Management
- Deviation Reporting
- Microsoft Word
- Microsoft Excel
- Continuous Improvement