Job Title: Deputy Director of Manufacturing Planning and Support
Location: Pearl River, NY
About the Job
Provides strategic leadership and operational oversight of manufacturing quality systems, production planning, and manufacturing support functions within a GMP biopharmaceutical environment. Responsible for ensuring compliance, operational efficiency, and continuous improvement across three distinct functional teams supporting manufacturing operations.
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.
Main Responsibilities
Manufacturing Quality Systems Leadership:
• Oversee manufacturing quality systems team responsible for deviation investigations, root cause analysis, and CAPA implementation
• Direct technical writing activities including SOPs, batch records, work instructions, and logbook management
• Ensure compliance with cGMP regulations and company quality standards
• Support regulatory inspections and audit readiness activities
Production Planning & Systems Management:
• Lead production planning team including scheduler and iShift/SAP specialist
• Oversee production scheduling, material planning, and manufacturing execution system operations
• Ensure accurate system transactions and data integrity in iShift and SAP platforms
• Coordinate with cross-functional teams to optimize production flow and resource utilization
Manufacturing Support Operations:
• Manage manufacturing support team responsible for buffer and solution preparation
• Oversee component preparation, glassware cleaning, and material readiness activities
• Ensure GMP compliance in all manufacturing support operations
• Drive continuous improvement initiatives across support functions
Leadership & Operational Excellence:
• Lead, develop, and mentor team managers and specialists across three functional areas
• Establish and monitor key performance indicators for quality, efficiency, and compliance
• Foster culture of safety, quality, and continuous improvement
• Manage resource allocation and workforce planning across multiple teams
About You
Education / Experience
• Bachelor's degree in Life Sciences, Engineering, Business Administration or related technical field required
• Advanced degree (MS, MBA, or PhD) Life Sciences, Engineering, Business Administration or related technical field - Preferred
• Minimum 10+ years biopharmaceutical manufacturing experience
• Minimum 5+ years progressive leadership experience in GMP environment
• Proven experience managing quality systems, production planning, or manufacturing support functions
• Deep understanding of cGMP regulations (21 CFR Parts 210, 211, 600)
• Experience with deviation management, technical writing, and batch record systems
• Knowledge of manufacturing execution systems (MES) and ERP platforms (SAP preferred)
• Understanding of buffer/solution manufacturing and component preparation processes
• Strong leadership and people development skills
• Excellent communication and cross-functional collaboration abilities
• Strategic thinking with strong execution capabilities
• Problem-solving and continuous improvement mindset
• Ability to work in manufacturing environment with cleanroom gowning
• Flexibility to respond to operational needs outside standard hours
Additional preferred Qualifications:
• Experience with vaccine or biologics manufacturing
• Six Sigma or Lean Manufacturing certification
• iShift and SAP system experience
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.
North America Applicants Only
The salary range for this position is:
$133.500,00 - $192.833,33All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.