Senior Project Manager

The Project Manager will play a pivotal role in the successful introduction and transfer of new products. Working within the New Product Program, this role is responsible for coordinating and executing multiple Technology Transfer projects, ensuring seamless integration between CQV and Manufacturing teams. The successful candidate will drive project deliverables, facilitate cross-functional collaboration, and ensure a robust process for bringing new products to commercial manufacturing.

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• Lead and support technology transfer activities for new products across several concurrent projects, ensuring compliance with site, corporate, and regulatory requirements.
  
• Act as a liaison between CQ, Manufacturing, and other stakeholder groups to coordinate timelines, deliverables, and documentation needs.
  
• Develop, maintain, and execute project plans, schedules, and risk assessments for Tech Transfer projects.
  
• Ensure manufacturing process readiness by working closely with both Manufacturing and CQ teams to identify, communicate, and resolve technical and quality-related issues.
  
• Coordinate Process Performance Qualification (PPQ), validation activities, and process handover plans.
  
• Track and report project progress, proactively managing risks, unforeseen changes, and problem resolution.
  
• Drive continuous improvement by capturing lessons learned and incorporating best practices across Tech Transfer initiatives.
  
• Support preparation and review of technical protocols, batch records, and required quality documentation.
  
• Present project updates and key metrics to management and cross-functional teams.
  
• Ensure activities meet EHS, GMP, and data integrity standards.
  

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• Bachelor’s degree or higher in Chemical Engineering, Biochemical Engineering, Life Sciences, or related field.
  
• 10+ years experience in pharmaceutical, biopharma, or a regulated manufacturing environment, ideally in a project engineering, process engineering, or tech transfer capacity.
  
• Strong knowledge of tech transfer methodology, scale-up, and validation within GMP-regulated environments.
  
• Proven experience collaborating across Manufacturing and Quality functions.
  
• Excellent project management, organizational, and communication skills.
  
• Knowledge of CQ, validation, and manufacturing operations.
  
• Experience with New Product Introductions and multi-product environments advantageous. xcfaprz
  
• Proficiency with project management software and MS Office tools.