QA Manufacturing Specialist I/II (4x10, 1900 - 0530)

jsrglobal· KBI Biopharma, Inc.
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📍 USA - CO - BoulderFull time💰 USD 67K–85K

About this role

Position Summary:

The Quality Assurance Specialist I/II Manufacturing is responsible for assuring products, processes, facilities, documentation, and systems conform to quality standards, internal procedures, systems, and governmental regulations. This position will provide a broad range of quality oversight for activities that support bulk drug substance manufacturing. This position will be responsible for review and approval of executed procedures, equipment logs, and batch records supporting all aspects of cGMP operations.

Position Responsibilities:

  • Perform compliance review on the following executed records: batch and solution record (includes on-the-floor review of records) and associated forms, in-process data, and applicable logs

  • Author new and revised Standard Operating Procedures, Forms/Logs, Master Batch Records and Solution Records

  • Support Manufacturing changeover process

  • Work directly with manufacturing, the laboratory and other departments responsible for GMP activities to resolve deviations and other compliance issues in a timely manner

  • Author, review, and approve deviation investigations

  • Support client batch record review process

  • Support QA Raw Material group with release of raw materials as needed

  • Able to react to change productively and handle other essential tasks as assigned.

Position Requirements:

  • QA Specialist I: Bachelor’s degree and 2 years of experience

  • QA Specialist II: Bachelor's degree and 6 years of experience

  • Experience in a cGMP QA environment or equivalent is preferred.

Salary: $67,000 - $85,000

This is a night shift position and will be eligible for a shift differential in addition to base salary.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Frequently Asked Questions

What is the salary for the QA Manufacturing Specialist I/II (4x10, 1900 - 0530) role at jsrglobal?
The listed salary for this QA Manufacturing Specialist I/II (4x10, 1900 - 0530) position at jsrglobal is USD 67K–85K. This is an Full time role.
Where is the QA Manufacturing Specialist I/II (4x10, 1900 - 0530) position at jsrglobal located?
This QA Manufacturing Specialist I/II (4x10, 1900 - 0530) role at jsrglobal is based in USA - CO - Boulder. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the QA Manufacturing Specialist I/II (4x10, 1900 - 0530) role at jsrglobal full-time or part-time?
This is listed as a Full time position. It is posted as a QA Manufacturing Specialist I/II (4x10, 1900 - 0530) role in the KBI Biopharma, Inc. department at jsrglobal.
Which team or department does the QA Manufacturing Specialist I/II (4x10, 1900 - 0530) at jsrglobal belong to?
This QA Manufacturing Specialist I/II (4x10, 1900 - 0530) position is part of the KBI Biopharma, Inc. department at jsrglobal. See the full job description for more information about the team structure and responsibilities.
How do I apply for the QA Manufacturing Specialist I/II (4x10, 1900 - 0530) position at jsrglobal?
Click the "Apply Now" button on this page. You will be redirected to jsrglobal's official application portal hosted on workday where you can submit your application directly.
When was the QA Manufacturing Specialist I/II (4x10, 1900 - 0530) job at jsrglobal posted?
This QA Manufacturing Specialist I/II (4x10, 1900 - 0530) position at jsrglobal was posted on Sep 18, 2026. Apply as soon as possible — early applications are often reviewed first.
QA Manufacturing Specialist I/II (4x10, 1900 - 0530)
jsrglobal · 💰 USD 67K–85K
Apply for this role ↗

You'll be redirected to jsrglobal's official application page on Workday.