Supply Chain Operations Manager

1 week ago

Mississauga, Ontario, Canada Pfizer, S.A. de C.V Full time
About the Role

Pfizer, S.A. de C.V is seeking a highly skilled and experienced Supply Chain Lead to join our team. As a key member of our organization, you will be responsible for leading the development and execution of investigational and commercial material global supply strategies for early and late-stage development programs.

Key Responsibilities
  • Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities required for the provision of investigational product on phase I-IV protocols for both Small Molecule and Biologics programs.
  • Provide consult on all aspects of investigational product strategies and be a key decision maker for the development of investigational product supply and sourcing strategies.
  • Oversee the end-to-end activities and identify potential risks while developing supply strategies that balance cost, timelines, and risks to support the development of candidates in the Pfizer Research & Development teams across multiple business units within Pfizer.
  • Accountable for Pfizer clinical supplies delivery and oversight of the end-to-end process from API to finished product delivery to clinical sites.
  • Manage clinical trial drug supply budget and communicate forecasts and changes effectively and in a timely fashion to study teams and GCS partner lines.
  • Ensure site and patient focus, along with quality compliance, throughout PharmSci and GCS processes.
  • Act as a point of contact for clinical supply required input during audits and regulatory inspections as well as participate in inspection readiness activities.
Requirements
  • Bachelor's Degree with 5 years of demonstrated and relevant experience in pharma/biotech project management and cross-functional team leadership; clinical supply project management experience preferred or a Master's Degree with 3 years of experience.
  • Demonstrated ability to manage large and complex clinical development programs.
  • Demonstrated capability to lead business development activities and acquisitions as they relate to clinical programs.
  • Demonstrated knowledge and experience working in a Good Manufacturing Practices (GMP) (cGMP) and Good Clinical Practices (GCP) (GxP) environment.
  • Demonstrated understanding of pharma quality and regulatory framework.
  • Demonstrated in-depth experience managing multiple clinical studies in parallel.
  • Demonstrated experience leading and delivering in a matrix team environment.
  • Working knowledge of MS office applications including MS Project and Office Timeline-Pro.
  • Demonstrated excellent computer, written, and verbal communication skills.
  • Demonstrated breadth of diverse leadership experiences and capabilities, including the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of colleagues to achieve meaningful outcomes and create business impact.
  • Demonstrated understanding of late-stage clinical drug development processes.
  • Demonstrated ability to inspire teams to deliver in a dynamic business environment through effective change management and leadership.
Preferred Qualifications
  • Relevant pharmaceutical experience.
  • Relevant operational experience across diverse business portfolio (e.g., Biopharmaceuticals, Consumer Products, other industries).
  • Past oral presentations at conferences and other large audiences.
What We Offer

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. We also offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments.

Relocation assistance may be available based on business needs and/or eligibility.

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.

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