Job Title: PCU Lead Support Services

Location: Framingham, MA

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 organization is the faithful execution of the current set of instructions, ensuring practice matches procedure, to assure high product quality and compliance with current cGMPs and Genzyme Quality standards, to always operate in a safe and environmentally sound manner, to develop and adhere to a production plan which supports a robust product supply, to continually improve processes, and to manage the budget.

• The PCU Lead Support Services sets operating plans and priorities for production that are aligned with our delivery objectives.
  
• The responsible person ensures appropriate resources are in place to fulfill near term goals and commitments while building towards sustainable manufacturing excellence.
  
• It is the responsibility of this position to oversee, direct and support the Manufacturing group according to Sanofi policies and to achieve business objectives that will have a major impact on the success of the Corporation.
  
• This individual is responsible for ensuring strong coordination and alignment between Manufacturing and support groups.
  
• Will develop strategies that ensure achievement of manufacturing objectives that are consistent with the site's strategic direction.
  
• Will develop and successfully manage to a production plan which supports a reliable product supply while upgrading the facilities and equipment and establishing capable, compliant manufacturing processes for area of responsibility.
  

• Bachelor's or master's degree and at least 15 years of progressive technical/operational leadership experience or equivalent is required.
  
• In-depth knowledge of biopharmaceutical, pharmaceutical, and/or device cGMP manufacturing is critical.
  
• Demonstrated ability to manage complex functional areas and achieve significant business results.
  
• Track record in successfully managing mid to large, complex manufacturing operations in the later stages of plant life-cycle.
  
• Demonstrated ability to develop self; build high performance teams, and develop others.
  
• Excellent communication skills and ability to influence and build relationships across the broadest constituencies both internal and external to the site.
  

• Track record in successfully managing manufacturing operations during multiple stages in the life-cycle of a manufacturing plant (start-up, growth, steady state and declining phases).
  
• Solid understanding of Health, Safety, Environmental and legal requirements for operations.
  
• Excellent problem solver and able to generate innovative solutions to a broad range of issues.
  
• Excellent people leadership and change leadership skills.
  
• Ability to set ambitious and realistic targets, drive execution and build culture of continuous improvement and accountability
  

• Ability to gown and gain entry to manufacturing areas.
  

• 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.