Company: KBI Biopharma
Posted on: January 5, 2022
Coordinate and perform cGMP manufacturing operations for
manufactured biopharmaceutical products.
Ensure the effective use of material, equipment andpersonnel while
making products at high quality levels.
Execute manufacturing processes without supervision & provide work
direction to less experienced personnel. Act as shift lead when
Must have in-depth knowledge and expertise in area
equipment/systems, as well as independently and fully developed
troubleshooting skills of equipment/processes.
Maintain records to comply with regulatory requirements, cGMPs and
Provide technical input of validation protocols, including
development, execution, and summary.
Ability to provide technical input into Batch Records
Train area personnel in one or more areas of expertise including
Responsibilities include hazardous and non-hazardous waste
Minimum HS/GED and 3+ year's related industry experience or BS/BA
and 2.5years+ experience or equivalent
Ability to add, subtract, multiply, and divide in all units of
measure, using whole numbers, common fractions, and decimals.
Ability to compute rate, ratio, and percent and to draw and
interpret bar graph
Ability to read and interpret English documents such as safety
rules, operating and maintenance instructions, procedure manuals,
batch and production records.
Ability to write routine reports and correspondence.
Ability to speak effectively before groups of customers or
employees of organization.
Ability to solve practical problems and deal with a variety of
concrete variables in situations where only limited standardization
Ability to interpret a variety of instructions furnished in
written, oral, diagram, or schedule form.
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
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
Keywords: KBI Biopharma, Boulder , Manufacturing Associate, Other , Boulder, Colorado
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