Superviseur(e), Production et Conformité / Supervisor, Production and Compliance

Jubilant Pharma, LLC; Montreal; On-site; CAD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Supervisor for Production and Compliance to ensure operational excellence in radiopharmaceuticals. This role is pivotal in managing compliance and driving improvements within the manufacturing environment. You will oversee production documentation, lead cross-functional initiatives, and support training efforts. Join a dynamic team dedicated to enhancing patient care through high-quality solutions. If you thrive in a fast-paced setting and are passionate about quality, this opportunity is perfect for you!

Qualifications

• 3+ years in regulated production, ideally in pharmaceuticals or biotech.
• Strong understanding of GMP and documentation control.

Responsibilities

• Manage production-related CAPAs and deviations ensuring compliance.
• Collaborate with QA and Validation for continuous improvement.

Skills

GMP Compliance

Problem Solving

Communication Skills

Organizational Skills

Leadership

Education

Bachelor’s degree in life sciences

Equivalent experience in GMP manufacturing

Tools

TrackWise

MasterControl

SAP

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Supervisor, Production and Compliance

Join our dynamic team at Jubilant Radiopharma as Supervisor, Production and Compliance ! We are seeking a driven individual who thrives in a fast-paced environment and is passionate about ensuring the highest standards of quality and compliance in our operations.

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.

Role Overview:

The Supervisor, Production and Compliance plays a critical role in ensuring compliance, operational excellence, and continuous improvement within the manufacturing environment. This role is responsible for managing and driving resolution of all production-related CAPAs, deviations, change controls, and documentation updates in accordance with GMP standards. Additionally, this position serves as a key backup to production supervisors, supporting day-to-day floor operations when needed.

Key Responsibilities:

• Own and manage all production-related CAPAs, deviations, and change controls from initiation to closure, ensuring timely completion and effectiveness.
• Maintain and update all production documentation (SOPs, batch records, logbooks, protocols) in alignment with quality and regulatory requirements.
• Serve as compliance point of contact for audits and inspections. Ensure readiness and compliance of production operations.
• Collaborate cross-functionally with QA, Validation, Engineering, and other departments to drive resolution of issues and continuous improvement initiatives.
• Act as a backup to production supervisors, providing operational oversight on the floor, supporting shift management, and ensuring continuity of manufacturing activities.
• Identify trends and systemic issues in quality events and lead initiatives to prevent recurrence and improve process robustness.
• Support training initiatives and ensure production teams are aligned with current procedures and compliance expectations.
• Participate in daily production and tiered meetings, contributing updates and supporting issue escalation and resolution.
• Supervise, coach, develop documentalist team members. Establish and monitor Key Performance Indicator for the team

Qualifications:

• Bachelor’s degree in life sciences, engineering, or related field preferred; equivalent experience in GMP manufacturing accepted.
• 3+ years of experience in a regulated production environment, ideally in pharmaceuticals, biotech, or Radiopharma.
• Solid understanding of GMP, deviation/CAPA management, and documentation control.
• Strong organizational, problem-solving, and communication skills.
• Demonstrated ability to lead cross-functional efforts and drive timely execution.
• Comfortable working on the production floor and stepping into operational leadership when required.
• Experience with radiopharmaceuticals (an asset)
• Experience with electronic quality management systems (e.g., TrackWise, MasterControl)
• Experience with Enterprise Resource Planning (e.g., SAP)
• Familiarity with lean manufacturing or continuous improvement methodologies
• Bilingual in French and English (must interact with regulatory agencies based outside Quebec (e.g. FDA))

Join Us:

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, Production and Compliance 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!