- Bachelor's Degree
- High School Diploma or GED
- Master's Degree
- Associate's Degree
- Leadership Experience
Paragon Bioservices, Inc. (PBI) is a growing biopharmaceutical contract development and manufacturing organization with an internationally recognized tradition of quality and service. PBI provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders as well as innovative start-ups utilizing novel technologies to produce state-of-the-art vaccines and therapies for people when they are most in need. As a PBI employee, you will actively contribute to the delivery of our services and products to our customers and their patients.
The Associate Director, Manufacturing for the Upstream Processing group is responsible to lead teams while overseeing the GMP manufacturing process, through the broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial systems for Phase I/II GMP manufacturing.
Key Responsibilities include but are not limited to:
Responsible for managing multiple teams of Supervisors, Team Leads & Associates across multiple campaigns and shifts
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:
HS Diploma or Associates Degree & 14 years of GMP biologic manufacturing experience OR B.S. in Engineering or Science discipline and 12+ years of GMP biologic manufacturing experience OR M.S. in Engineering in a Science discipline plus 10+ years of GMP biologic manufacturing experience. Some or all of this experience should be in upstream processing.
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) required
Minimum of 6 years of leadership experience required (HS Diploma/Assoc degree); 4 years leadership (Bachelor or Master’s degree).
Paragon Bioservices is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.