Manufacturing Associate III
Boulder, CO - USA
Job Summary
Position Summary:
The Manufacturing Associate I/II is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written approved procedures and forms to ensure all work is conducted Right First Time (RFT) following Good Manufacturing Practice (GMP) including good documentation practices and/or Good Laboratory Practice (GLP).
Position Schedule:
This position is for a Manufacturing Associate I/II working 6:00 AM - 6:30 PM on a 2 - 2 - 3-day shift schedule.
Responsibilities:
- Manufacture bulk intermediates and drug substances per manufacturing batch records and 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 records and logbooks following GDP at the time of execution.
- Utilize and perform maintenance on equipment per applicable SOP.
- Ensure all materials are issued and accounted for during the execution of a record (i.e. SPR BPR and Forms).
- Demonstrate apply and ensure understanding of cGMP and how it applies to specific tasks and responsibilities.
- Participate and be accountable for workplace organization (5S).
Requirements:
- Manufacturing Associate I: Bachelors degree in a related scientific or engineering discipline and 0-2 years experience in related cGMP manufacturing operations; or high school degree and 3-5 years experience or equivalent.
- Manufacturing Associate II: Bachelors degree in a related scientific or engineering discipline and 2-5 years experience in related cGMP manufacturing operations; or high school degree and 4-6 years experience or equivalent.
Salary Range:
- Manufacturing Associate I: $26.44 - $36.49
- Manufacturing Associate II: $30.29 - $41.78
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.
Required Experience:
IC
About Company
KBI Biopharma Inc. is a global contract development and manufacturing organization (CDMO / CMO) offering Cell Line Development, Process Analytical & Formulation Development, Clinical & Commercial Manufacturing, and more.