Biopharma Manufacturing Associate I/II — Day Shift

KBI Biopharma, Inc.

Boulder (CO)

On-site

USD 36,000 - 58,000

Full time

14 days+

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Job summary

KBI Biopharma, Inc. is seeking a Manufacturing Associate I/II to perform upstream or downstream processing of bulk intermediates and drug substances. The role follows approved procedures to ensure Right First Time in GMP/GLP environments, with responsibilities spanning aseptic processing, documentation, equipment maintenance, and strict material accounting.

A 2-2-3 shift pattern applies. The position requires a degree in a related scientific or engineering field and relevant experience, or a

Qualifications

  • Bachelor's degree in a scientific or engineering field with 0–2 years' experience in cGMP manufacturing for Associate I; or high school with 3–5 years' related experience for Associate I.
  • Bachelor's degree with 2–5 years' experience in cGMP manufacturing for Associate II; or high school with 4–6 years' related experience for Associate II.
  • Experience following GMP/GLP, GDP documentation, and adherence to SOPs.

Responsibilities

  • Manufacture bulk intermediates and drug substances per batch records and quality standards.
  • Perform aseptic operations in cleanroom environment, including gowning and cleaning protocols.
  • Document manufacturing tasks in records and logbooks using GDP at execution.
  • Operate and maintain equipment per applicable SOPs.
  • Ensure materials are issued and accounted for during record execution (SPR, BPR, Forms).
  • Demonstrate understanding of cGMP and its application to tasks and responsibilities.
  • Support and participate in workplace organization (5S).

Education

Bachelor's degree in related scientific or engineering discipline
High school diploma with related cGMP manufacturing experience

Job description

KBI Biopharma, Inc. is seeking a Manufacturing Associate I/II to perform upstream or downstream processing of bulk intermediates and drug substances. The role follows approved procedures to ensure Right First Time in GMP/GLP environments, with responsibilities spanning aseptic processing, documentation, equipment maintenance, and strict material accounting.

A 2-2-3 shift pattern applies. The position requires a degree in a related scientific or engineering field and relevant experience, or a

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