Manufacturing Associate I/ii-upstream-3

KBI Biopharma

Durham, NC, United States
Upstream processing
Good manufacturing practice
Bioprocessing equipment
The Manufacturing Associate is responsible for performing upstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products

Job Summary

  • The Manufacturing Associate is responsible for performing upstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products.
  • Staff will work cross-functionally with QA, MS&T, facilities, engineering, supply chain, IT, AFS, and other key departments to ensure successful manufacturing operations.
  • A proven Manufacturing Associate will demonstrate learning agility, results-driven orientation, and strong attention to detail.

Matching Summary

The Manufacturing Associate is responsible for performing upstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products.

Skills & Requirements

Must-have

  • upstream processing
  • Good Manufacturing Practice
  • bioprocessing equipment

Nice-to-have

  • single-use platform technology
  • excellent communication skills
  • fast-paced environment

Key Requirements

  • Bachelor’s degree in a related scientific discipline
  • 0-5 years’ experience in cGMP manufacturing operations
  • basic knowledge of upstream processing

Work Rights

Not specified

Tailored Resume

Cover Letter