Job Description

Reference No. R2662210

Position Title: Finished Good Product Lifecycle Manager - Vaccines

Department: Supply Chain Product Portfolio Management

Location: Sanofi Pasteur Limited, Toronto

Sanofi Pasteur: The world's leading vaccine company

Sanofi Pasteur, the vaccines division of Sanofi, is the largest company in the world devoted entirely to human vaccines. Our driving goal is to protect people from infectious diseases by creating safe and effective vaccines. Our company distributes more than 1 billion doses of vaccine each year, making it possible to vaccinate more than 500 million people across the globe. Sanofi Pasteur offers the broadest range of vaccines in the world, providing protection against 20 bacterial and viral diseases.

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

Position Summary:

The Finished Good Product Lifecycle Manager oversees delivering projects on time and on budget, in accordance with the Finished Good Product Lifecycle Management Process. The scope of projects ranges from new product launches and market extensions to discontinuation of products within markets where licenses are withdrawn. The role has in scope a broad range of activities from establishing project plans to leading the coordination of Toronto activities required to deliver such projects.

Key Responsibilities:

Develop and manage project plans within the Finished Good Product Lifecycle Management Process in collaboration with cross-functional areas and stakeholders.

Proactively monitor and control project execution to ensure all project objectives milestones are met within the agreed upon timelines.

Maintain documentation (I.e. SOPs, Market Specifications).

Perform project risk assessment and identify mitigation plans with support.

Lead product launch/discontinuation forums, working groups, interact with cross functional teams in production, quality operations, site supply chain/material planners, Convergence, global demand, RA, Artwork in TOR, other sanofi sites, or other local or global functions, as needed, to support timely and compliant product lifecycle changes.

Execute the License Compliance Verification to ensure compliant product launches in collaboration with cross function teams.

Lead the Change control process (CCR Leader) for changes within Finished Good Product Lifecycle Management scope.

HSE REQUIREMENT/STATEMENT

Contribute to maintaining the level of compliance with all cGMP regulatory standards and comply with all sanofi pasteur procedures and policies related to Quality, Health, Safety and Environment.

Major Challenges:

Interfacing with multiple functions, including production, quality operations, Convergence, global demand, Artwork,

Regulatory Affairs, Global functions and other site counterparts.

Fast paced environment, linked projects and competing priorities (e.g. coordination of multiple projects and planning with conflicting stakeholder's priorities).

Assist with complex regulatory submissions (Regulatory Submission Review).

Managing License compliance verification process with Regulatory Affairs to ensure submissions impacting launch lot are approved prior to launch.

Dimensions/Scope:

Breadth of responsibility: Toronto site level. Will include participation in global initiatives as needed.

This position also works with other sites' counterparts to build synergy and continuous improvement and ensure timely execution of inter-site projects i.e. product launches.

Lead the coordination of activities in Toronto to enable the global launch of Acel products, mainly driven by Adacel, which represents a volume growth of 82% (41Mds to 75Mds) and a revenue growth of 50% (865 MEUR to 1,289 MEUR) to 2025.

No direct reports.

Lead cross-functional forums.

Key Requirements:

University degree such as Bachelor of Science, Bachelor of Engineering or Business studies.

8 years' experience in Pharmaceutical with, Quality, Production and/or Supply Chain roles.

Expertise in project management.

Good understanding of Good Manufacturing Practices, cGMPs, regulatory impact.

Advanced skills of Excel and MS 365 applications (MS Project).

Excellent oral and written communication skills; competent presentation skills a must.

Good interpersonal (influencing) and facilitation skills required.

Conflict resolution in group dynamics.

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request.

Thank you in advance for your interest.

Only those candidates selected for interviews will be contacted.

Sanofi, Empowering Life

#GD-SP #LI-SP

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.