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Hourly Upstream Manufacturing Associate Jobs in Colorado

48forty Solutions

Manufacturing Associate

Henderson, CO · On-site

$15.16 - $25/hr

Hourly Pay: $19.50/hr. During Training 60 days and then $16.00/hr. + Piece rate (AVG $21.00/hr. - $31.00/hr. Shift(s): 1st Shift: Monday- Friday 7:00am - 4:00pm Location: 8221 East 96th Avenue, Unit ...

48forty Solutions

Manufacturing Associate

Henderson, CO

$21 - $31/hr

Hourly Pay: $19.50/hr. During Training 60 days and then $16.00/hr. + Piece rate (AVG $21.00/hr. - $31.00/hr. Shift(s): 1st Shift: Monday- Friday 7:00am - 4:00pm Location: 8221 East 96th Avenue, Unit ...

48forty Solutions

Manufacturing Associate

Henderson, CO

$15.16 - $25/hr

Hourly Pay: $19.50/hr. During Training 60 days and then $16.00/hr. + Piece rate (AVG $21.00/hr. - $31.00/hr. Shift(s): 1st Shift: Monday- Friday 7:00am - 4:00pm Location: 8221 East 96th Avenue, Unit ...

TriMas Corporation

Automation Technician

Denver, CO · On-site

$30 - $38/hr

Hourly Full-Time Function: Engineering Equal Opportunity Employer Minorities/Women/Veterans ... or manufacturing. * Associate degree or technical certification in Mechatronics, Industrial ...

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Hourly Upstream Manufacturing Associate information

What is the difference between Hourly Upstream Manufacturing Associate vs Upstream Manufacturing Technician?

AspectHourly Upstream Manufacturing AssociateUpstream Manufacturing Technician
CredentialsHigh school diploma or equivalent; GMP training often requiredHigh school diploma; GMP and technical training
Work EnvironmentManufacturing floor, repetitive tasks, team-basedManufacturing floor, technical troubleshooting, equipment operation
Employer & Industry UsageBiotech and pharmaceutical manufacturingBiotech and pharmaceutical manufacturing
Common Search & ComparisonYesYes

The main difference between an Hourly Upstream Manufacturing Associate and an Upstream Manufacturing Technician lies in their roles and responsibilities. Associates typically perform routine manufacturing tasks under supervision, focusing on production line activities. Technicians often have more technical training, handle troubleshooting, and maintain equipment. Both roles are essential in biotech manufacturing, with similar credentials and work environments, but technicians usually require additional technical skills.

What are popular job titles related to Hourly Upstream Manufacturing Associate jobs in Colorado? For Hourly Upstream Manufacturing Associate jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Hourly Upstream Manufacturing Associate jobs in Colorado look for? The top searched job categories for Hourly Upstream Manufacturing Associate jobs in Colorado are:
What cities in Colorado are hiring for Hourly Upstream Manufacturing Associate jobs? Cities in Colorado with the most Hourly Upstream Manufacturing Associate job openings:
Hourly Upstream Manufacturing Associate jobs near you
KBI: US - Manufacturing Associate I/II

KBI: US - Manufacturing Associate I/II

KBI Biopharma, Inc.

Boulder, CO

$30.29 - $41.78/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago

KBI Biopharma rating

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.


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.

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).


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: Bachelor's 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: Bachelor's 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


Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.

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.

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