Supervisor II - Manufacturing
- Greater Montreal Metropolitan Area, QC, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Experience
- Minimum of 4 years experience in the pharmaceutical industry with a minimum of 2 years in a supervision role (unionized environment).
- Posting language
- English
- Posted
Original job description
Job Description
Job Title: Supervisor II - Manufacturing
Req Id: 2176
Posting Start Date: 11/13/26
Job Description:
Why Jubilant Radiopharma?
At Jubilant Radiopharma, we are dedicated to making a meaningful impact in the lives of patients by delivering high-quality radiopharmaceuticals. As a leader in the industry, we offer exciting opportunities for professional growth and development, along with a collaborative work environment where your contributions are valued and recognized.
The Position
The supervisor is responsible for coordinating and executing production batches of radiopharmaceutical products in compliance with customer orders and Good Manufacturing Practices. The supervisor must ensure that the required internal standards as well as the requirements from regulatory agencies, health and safety, and radioprotection are rigorously respected. The supervisor must establish and maintain a culture of quality throughout production operations and skillfully manage work to ensure good working relationships and employee engagement.
The hours for this position will be 4 days per week, Monday to Thursday from 1:00 pm to 11:00 pm.
Key Responsibilities
Team Management:
Qualifications:
If you are looking for a challenging yet rewarding opportunity to make a difference in the healthcare industry, we invite you to apply for the Supervisor, Manufacturing position at Jubilant Radiopharma. Join us in our mission to deliver innovative solutions that enhance patient care and improve lives. Apply now and be part of our success story!
Job Title: Supervisor II - Manufacturing
Req Id: 2176
Posting Start Date: 11/13/26
Job Description:
Why Jubilant Radiopharma?
At Jubilant Radiopharma, we are dedicated to making a meaningful impact in the lives of patients by delivering high-quality radiopharmaceuticals. As a leader in the industry, we offer exciting opportunities for professional growth and development, along with a collaborative work environment where your contributions are valued and recognized.
The Position
The supervisor is responsible for coordinating and executing production batches of radiopharmaceutical products in compliance with customer orders and Good Manufacturing Practices. The supervisor must ensure that the required internal standards as well as the requirements from regulatory agencies, health and safety, and radioprotection are rigorously respected. The supervisor must establish and maintain a culture of quality throughout production operations and skillfully manage work to ensure good working relationships and employee engagement.
The hours for this position will be 4 days per week, Monday to Thursday from 1:00 pm to 11:00 pm.
Key Responsibilities
Team Management:
- Manage and motivate the team towards achieving objectives and lead the appropriate action plan required to reach the desired goals.
- Ensure appropriate communication with support services such as quality, engineering, technical services, etc., to support the team in achieving objectives.
- Ensure continuous training and development of the team.
- Responsible for cGMP training for new employees as well as ongoing cGMP training for existing employees.
- Manage absenteeism and overtime.
- Ensure an active presence on the floor with employees.
- Increase the level of autonomy and participation of production employees.
- Manage production operations considering the number of employees, their level of knowledge and experience, radiation exposure, and the various tasks to be accomplished.
- Generate the monthly report on production performance indices.
- Manage the inventory of raw materials, considering expiration dates, delivery, analysis delays, and optimal quantities to order.
- Issue the weekly report on HVAC monitoring.
- Review standard operating procedures (SOPs), production records, validation protocols and reports, change controls, and non-conformities.
- Conduct investigations with a valid scientific basis and problem-solving within the expected timeframes and ensure everything is appropriately documented. Provide necessary data for the APQR process.
- Participate in the improvement of manufacturing operations, materials, and equipment.
- Send work requisitions for calibration and repair of instruments.
- Manage precautionary cleaning.
- Support SAP activities related to production.
- Delegate work assignments to meet weekly production schedules.
- Actively participate in developing a quality culture among all production employees.
- Train all employees on behaviors related to quality and improvements.
- Ensure proper execution of operations (preparation, maintenance, etc.) according to procedures and in compliance with cGMP.
- Responsible for the application and compliance with health and safety rules and regulations.
- Responsible for the application and compliance with radioprotection rules and regulations.
Qualifications:
- B.Sc. or M.Sc. in science or chemical engineering
- Minimum of 4 years experience in the pharmaceutical industry with a minimum of 2 years in a supervision role (unionized environment).
- Very good knowledge of GMP (Good Manufacturing Practices).
- Proficient in Microsoft Word and Excel.
- French (written and spoken)
If you are looking for a challenging yet rewarding opportunity to make a difference in the healthcare industry, we invite you to apply for the Supervisor, Manufacturing position at Jubilant Radiopharma. Join us in our mission to deliver innovative solutions that enhance patient care and improve lives. Apply now and be part of our success story!
More about this job
Responsibilities
Coordinate and oversee radiopharmaceutical production batches, ensuring compliance with customer orders, cGMP, regulatory requirements, and health and radioprotection rules. Lead and develop production employees, manage schedules and materials, review production and quality documentation, investigate issues, and support continuous improvement.
Requirements
A B.Sc. or M.Sc. in science or chemical engineering is required, along with at least four years of pharmaceutical industry experience, including at least two years in a supervisory role in a unionized environment. Candidates should have very good GMP knowledge, proficiency in Microsoft Word and Excel, and French written and spoken skills.
Skills
- Team Management
- Production Operations
- Good Manufacturing Practices
- cGMP Training
- Quality Management
- Regulatory Compliance
- Radioprotection
- Health and Safety
- Inventory Management
- Scientific Investigation
- Problem-Solving
- Standard Operating Procedures
- Microsoft Word
- Microsoft Excel
- SAP
- French
Visa sponsorship
Not detected in the job text
Categories
- Manufacturing
- Management & Leadership
- Healthcare
- Science & Research
- Security & Safety
Keywords
- Radiopharmaceuticals
- Pharmaceutical Manufacturing
- Good Manufacturing Practices
- cGMP
- Regulatory Compliance
- Radioprotection
- Health and Safety
- Production Batches
- Production Scheduling
- Team Supervision
- Employee Training
- Quality Culture
- Inventory Management
- Raw Materials
- Standard Operating Procedures
- Production Records
- Validation Protocols
- Change Controls
- Non-Conformities
- Scientific Investigations
- APQR
- HVAC Monitoring
- Calibration
- SAP
- Microsoft Word
- Microsoft Excel
- French
- Unionized Environment