Manager, Upstream GMP Manufacturing

Paragon Bioservices   •  

Baltimore, MD

Industry: Pharmaceuticals & Biotech


8 - 10 years

Posted 281 days ago

This job is no longer available.

Key Responsibilities include but are not limited to: 

  • Responsible for managing a team of professional production associates
  • Oversight of upstream production operation for cell culture or microbial processes
  • Ensures the successful technical transfer of projects from the Tech transfer group to the GMP production group
  • Works closely with the production staff to troubleshoot process and equipment problems
  • May create, revise, and edit SOP, SMPs, and specs as needed
  • Actively participates in all recruiting efforts to secure, onboard and develop new staff members
  • Facilitates GMP and Safety training of GMP staff, with a focus on cross-training and continuous improve and production records
  • Generates operational protocol(s) and production records
  • Works closely with senior management to initiate new production projects and assists in developing processes/techniques to meet contract objectives
  • Will overview PD materials, equipment, methods for GMP compliance and scalability
  • Expands the technical capabilities of the GMP Group
  • Effectively communicates results of departmental work through team discussions and documentation Other duties as assigned
  • Interacts with clients on presentations and project results; will also work closely with clients during initial and subsequent manufacturing campaigns
  • Recommends equipment, supply purchases within the production areas

Skills & Behaviors: 

  • Has considerable knowledge/expertise relevant to fundamental lab technologies, particularly focused on protein expression, isolation and analysis
  • Has excellent understanding and knowledge of microbial fermentation, centrifugation, operations of reactors and TFF processes OR Have excellent understanding and knowledge of cell culture techniques and processes, experienced in using disposable single-use bioreactors (WAVES, Xcellerex)
  • Has demonstrated track record of managing hands-on cGMP manufacturing operations
  • Experience and a thorough understanding of coordinating manufacturing activities with other departments (QA, QC) to maintain internal and project schedules
  • Ability to produce successful results in a fast-paced environment, under minimal supervision while leading a team of professional production associates
  • Creative individual with excellent troubleshooting skills as they relate to scientific and engineering principles 

Experience & Education: 

  • B.S. in Engineering or Life Science discipline plus 8+ years of relevant experience OR M.S. in Engineering in a Life Science discipline plus 6+ years of relevant experience
  • Microbial:  Experience with microbial (bacteria, yeast) production & fermentation processes to produce bulk biologics (proteins, polysaccharides, antibodies, etc.) OR Cell Culture: cell culture techniques and processes, experienced in using disposable single-use bioreactors (WAVES, Xcellerex)
  • Minimum of 3 years of supervisory experience