Job title: Production scheduler
Location: Pearl river, NY
About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The primary responsibility of the manufacturing Production Scheduler is to ensure the timely scheduling and execution of all activities related to the production and delivery of Flublok drug substance. This position requires strong cross-functional collaboration with Manufacturing, Supply Chain, Quality, HSE, and Facilities teams to create and maintain an optimized production schedule that aligns with the overall supply plan. The Scheduler will ensure that the schedule is not only accurate but also adaptable to changing conditions, providing full visibility to all relevant functions to ensure seamless operations and on-time delivery.
The scheduler promotes a culture of collaboration, encouraging open communication, speaking up, and thoughtful risk-taking to empower teams in decision-making and problem-solving.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
Schedule Management: Develop, maintain, and adjust the production schedule for Flu Blok drug substance, ensuring all manufacturing activities are aligned with supply chain requirements and production goals.
Cross-Functional Collaboration: Work closely with Manufacturing, Supply Chain, Quality, HSE, and Facilities teams to gather input, address potential bottlenecks, and ensure that all departments are aligned on timelines and deliverables.
Accuracy & Visibility: Ensure the production schedule is consistently 100% accurate and up to date, providing clear visibility to all stakeholders across functions. Proactively address any discrepancies or delays in real-time to minimize impact on the overall production process.
Continuous Improvement: Monitor scheduling processes for opportunities to optimize and streamline workflows, minimizing downtime and improving efficiency.
Problem-Solving & Issue Resolution: Act as the first point of contact for scheduling-related issues, identifying and addressing challenges promptly to prevent disruptions to the manufacturing process.
Data Reporting & Analysis: Maintain scheduling reports and performance metrics, providing detailed status updates and insights to leadership teams as required.
About You
Experience:
Bachelor’s degree in Life Sciences, Engineering or other related field required.
Experience in production scheduling or manufacturing coordination, ideally in a pharmaceutical or life sciences environment preferred.
Proficiency in scheduling software and Microsoft Office Suite and experience with ERP (SAP) systems.
Languages:
English
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.