The Technical Project Manager will have a strong technical and/or operations background in cGMP manufacturing in the pharmaceutical, biologic, medical device, or combination product industries. Responsibilities include providing technical project management support on client projects, overseeing cross-functional teams, and ensuring project deliverables are completed in compliance with relevant standards and regulations.
Requirements
- Bachelor of Science Degree in Chemical, Biomedical, or Mechanical Engineering, or related technical discipline from an accredited institution.
- 2+ years Project Management or Program Management experience
- 4+ years of proven experience in the biopharma and/or medical device industries (i.e., Life Science) with knowledge in two or more of the following practice areas: CGMP Manufacturing, Validation, Quality Engineering, Process Engineering, Quality Control or Analytical Science, Quality Assurance, Regulatory Affairs, Technology Transfer, Clinical or Medical Services, Late Stage Process or Product Development
