PMO Project Manager III

Responsibilities

• Lead end-to-end execution of technology transfers (TT), site switches, and major lifecycle projects at Contract Manufacturing Organizations (CMOs/CDMOs).
• Ensure flawless planning and execution of scale-ups, validation, and launches.
• Create comprehensive project plans including scope, timelines, cost, resources, and risk management.
• Manage project budgets and ensure all deliverables align with Teva’s compliance and operational standards.
• Facilitate seamless integration across R&D, MS&T, Quality, Supply Chain, Finance, and the CMO network.

Requirements

• Bachelor’s degree in Engineering, Life Sciences, Pharmacy, Chemistry, or a related field.
• 5+ years of experience in pharma operations, external manufacturing, MS&T, or project management.
• Proven experience leading complex technical projects within GMP environments.
• Strong knowledge of technology transfer, validation processes, and regulatory expectations.
• Excellent leadership and communication skills.

Preferred Qualifications

• Advanced degree such as an MBA, MS, or specialized Engineering/Regulatory degree.
• Experience with OSD, LCO, sterile/aseptic operations, or complex generics.
• PMP, PRINCE2, Lean Six Sigma, or PgMP certification.
• Direct experience working with CMOs or CDMOs.

Benefits

• Comprehensive medical insurance, OPD coverage, and annual health checkups.
• Term life and accident insurance.
• Confidential emotional wellbeing support through the Optum Employee Assistance Program.
• Opportunities for global collaboration and professional development through the R&D Academy and mentorship programs.

About the Company

Teva is a leading innovative biopharmaceutical company dedicated to addressing patients' needs worldwide. We foster a high-performing, inclusive culture that values fresh thinking, collaboration, and the opportunity to better health globally.