Directeur(trice) associé(e), Production / Associate Director, Production

at  Jubilant Pharma Holdings Inc

QUALIFICATIONS :

• Baccalauréat en sciences ou en ingénierie, y compris un cours de microbiologie.
• Au moins 10 ans d’expérience dans un environnement de production pharmaceutique.
• Au moins 5 ans d’expérience en gestion.
• Une expérience des produits radiopharmaceutiques est un atout.
• Une expérience de la gestion d’employés syndiqués est un atout.
• L’expérience de la fabrication stérile est un atout.
• Bilingue, tant à l’écrit qu’à l’oral, en français et en anglais.

ASSOCIATE DIRECTOR, PRODUCTION

Join our dynamic team at Jubilant Radiopharma as Associate Director, Production! 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.

QUALIFICATIONS:

• Bachelor’s degree in Science or Engineering including a microbiology course.
• Minimum 10 years of experience within a Pharmaceutical manufacturing environment.
• Minimum 5 years management experience.
• Experience with radiopharmaceuticals is an asset.
• Experience in managing unionized employees is an asset.
• Experience in sterile manufacturing is an asset.
• Bilingual both written and spoken in French and English.

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 Associate Director, Productionposition 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 Overview

ROLE OVERVIEW:

As Associate Director, Production, you will be at the forefront of production, responsible for all aspects of manufacturing to ensure that products are produced safely, efficiently and in compliance with all quality and regulatory requirements as well as company policies. The Associate Director is expected to play a critical role ensuring that departmental activities meet the current business needs with regards to external and internal customers and ensuring that development plans meet future business requirements. He/she is in charge of the manufacturing, warehousing and shipping of sterile and non-sterile products. The individual works closely with several representatives from Quality (QC and QA), Customer Service, Supply Chain, Validation, Maintenance and Technology Transfer.

KEY RESPONSIBILITIES:

• Ensure that effective manufacturing plans and processes are in place to meet JDI customer service targets with respect to quality and on-time delivery.
• Identify potential impediments to business schedule completion and provide direction and guidance to the department to overcome issues and difficulties while working closely with all other departments.
• Implement appropriate tools, processes and controls in order to ensure that the department is fully compliant with regards to current Good Manufacturing Practices (cGMP), corporate policies, Health and Safety regulations as well as Radioprotection regulations.
• Foster the development of a team oriented and empowerment approach to develop and maintain an environment that emphasizes accountability and self-compliance.
• Develop a plan to further strengthen Quality culture and embed it into day-to-day activities.
• Establish, monitor and improve Key Performance Indicators (KPIs) for the department, review performance data and quality metrics and implement corrective actions to meet objectives.
• Translate future business needs into mid-term and long term strategic plans for the production department while ensuring alignment with the Manufacturing Operations and Draximage strategy and vision.
• Actively work on the short and medium term production planning to ensure alignment between all department and support customer needs
• Work with Technology Transfer departments to define and implement improvements to existing manufacturing processes and equipment.
• Responsible for the creation and update of all production documentation (Master batch records, Bill of Material, SOP’s, equipment calibration) and the review of production related documentation (validation protocols and reports)
• Build a solid technical knowledge of the processes and products portfolio.
• Ensure that all production employees are properly trained and qualified to execute their duties through training plan and performance monitoring.
• Recruit, train and develop direct reports to ensure a strong and autonomous production team.
• Ensure compliance of the team with regards to union agreement and employment policies.
• Develop and track the annual and long-term production operational and capital budgets.
• Can replace at times any direct reports and assist supervisors in the day-to-day activities.
• Respond to manufacturing, radiation safety and SAP-related emergencies.