Purification unit operations jobs

Manufacturing Associate I

KBI Biopharma · Posted Nov 11, 2026

Durham, North Carolina, United States
On-site
Full-time · Entry
0–5 years

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The Manufacturing Associate I is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment.

Responsibilities

Manufacture cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations.
Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR)
Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.

Requirements

Bachelor’s degree in a related scientific or engineering discipline
High school diploma
Nice to have: Single-use platform technology

Skills

GMP GDP GLP Aseptic technique

Manufacturing Associate I/II

Manufacturing Associate I/II

Responsibilities

Requirements

Skills

Manufacturing Associate I

Responsibilities

Requirements

Skills