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Senior Manager, Program Management Lead

2 months ago


Albany, New York, United States AmplifyBio Full time
About the Role

We are seeking an experienced and dynamic Program Management Group Lead to join our Technical Operations team at AmplifyBio.

The successful candidate will oversee a team of project managers and drive the successful execution of multiple client programs across our advanced therapy portfolio.

Key Responsibilities
  • Lead, recruit, train, and develop project managers, ensuring that team members possess the necessary skills and expertise to manage multiple client projects.
  • Provide strong leadership and direction to the program management team, fostering a culture of innovation, collaboration, and excellence.
  • Develop and implement program management strategies aligned with our Contract Manufacturing (CMC) objectives and client needs.
  • Oversee the planning, execution, and delivery of multiple cell and gene therapy programs simultaneously.
  • Establish and maintain strong relationships with clients, internal stakeholders, and cross-functional teams.
  • Manage program budgets, timelines, and resources to ensure optimal utilization and client satisfaction.
  • Implement and refine program management processes, tools, and best practices specific to advanced therapy development and manufacturing.
  • Identify and mitigate risks across programs, developing contingency plans as needed.
  • Provide regular status updates and reports to senior management and clients.
  • Implement tools and oversee the coordination of manufacturing schedules, production runs, and plant operations to meet program timelines and deliverables.
  • Ensure compliance with Good Manufacturing Practice (GMP) regulations, quality standards, and safety protocols in all program activities.
Requirements
  • Bachelor's degree in Life Sciences, Biotechnology, or related field; Master's degree preferred.
  • Minimum 8 years of experience in program management within the biopharmaceutical industry.
  • Proven track record of leading and developing high-performing teams.
  • Strong understanding of cell and gene therapy development and manufacturing processes.
  • Excellent knowledge of GMP regulations and quality systems applicable to Contract Development and Manufacturing Organizations (CDMOs).
  • Demonstrated ability to manage complex, multi-faceted programs in a fast-paced environment.
  • Exceptional communication, negotiation, and stakeholder management skills.
  • Proficiency in project management software and tools.
  • PMP certification or equivalent is highly desirable.
What We Offer
  • Competitive Compensation Package
  • Health, Dental, and Vision insurance
  • FLEXIBLE PTO policy
  • Generous paid parental leave
  • Wellness and Self-Care Programs
  • 401(k) match
  • Tuition Reimbursement
  • EAP/work-life support system
  • A fun work environment where everyone's voice matters