BioProcess Associate

Emergent Biosolutions•Canton, MA

1d•$58,000 - $70,300•Onsite

About The Position

The Bioprocess Associate position reports to Supervisor/Manager Manufacturing. Prior experience in GMP manufacturing, including operation of GMP process equipment and documenting in a GMP compliant manner. This role is responsible for supporting the overall GMP manufacturing process that may include Central Services, Upstream, Downstream, or Final Formulation.

Requirements

Bachelor’s degree in a Scientific, Engineering or Biotech field typically with 2+ years’ experience with biologic production processes under GMP compliance or equivalent commensurate experience.
Outstanding knowledge, and ability to apply scientific principles utilized to solve operational, as well as routine production tasks.
Excellent documentation skills including comprehension & execution of Batch Production Records, SOP’s and forms.

Responsibilities

Operates pharmaceutical manufacturing equipment such as autoclaves, parts washers, filter integrity testers, incubators, stainless steel bioreactors, centrifuges, TFF skids, and in process testing equipment.
Ability to operate in an aseptic manner within a BioSafety Cabinet.
Demonstrates, understands and adheres to Emergent policies, GMP standards and safety procedures.
Communicates effectively with team members and supervisors regarding status of daily production tasks.
Executes documentation for logbooks, forms, solution prep and batch records according to GMP and site quality standards.
May assist in revision of GMP Documentation.
Perform cleaning and organization of the manufacturing cleanrooms. Ensures the areas are audit ready at all times.
Supports Emergent QA during audits and regulatory inspections.
Supports other manufacturing process teams and cross functional partners as necessary to achieve Manufacturing team goals.