ZipRecruiter

Log In

1

Day Shift Upstream Manufacturing Associate Jobs in Colorado

Vestas

Manufacturing Associate I Day

Windsor, CO · On-site

$23.50 - $28/hr

Production Team Member - Days Join our dynamic team at the Windsor Production facility, where we're ... Thurs, Friday, Saturday and every other Wednesday, 6am-6:30pm Orange Shift: Sunday, Mon, Tues and ...

Vestas

Manufacturing Associate II Day

Windsor, CO · On-site

$23.50 - $28/hr

The components manufactured at our Windsor factory are used primarily in Turbines in North America ... Thurs, Friday, Saturday and every other Wednesday, 6am-6:30pm Orange Shift: Sunday, Mon, Tues and ...

next page

Showing results 1-20

All JobsDay Shift Upstream Manufacturing Associate JobsDay Shift Upstream Manufacturing Associate Jobs in Colorado

Day Shift Upstream Manufacturing Associate information

What is a day shift upstream manufacturing associate?

A Day Shift Upstream Manufacturing Associate is responsible for preparing and operating equipment to support the initial stages of biopharmaceutical production, typically involving cell culture, fermentation, and media preparation. Working during the day shift, they monitor processes, maintain sterile environments, and ensure production runs smoothly and efficiently. Their work is crucial in ensuring quality and consistency in the early phases of manufacturing biological products such as vaccines or therapeutic proteins.

What are the key skills and qualifications needed to thrive as a day shift upstream manufacturing associate?

To excel as a Day Shift Upstream Manufacturing Associate, you typically need a background in biotechnology or life sciences, experience with aseptic techniques, and an understanding of Good Manufacturing Practices (GMP). Familiarity with bioreactors, cell culture systems, and process control software is commonly required, along with relevant safety or GMP certifications. Attention to detail, teamwork, and strong problem-solving abilities are valuable soft skills in this role. These competencies ensure the efficient and compliant production of high-quality biopharmaceuticals in a regulated manufacturing environment.

What are the typical collaboration points between a day shift upstream manufacturing associate and other teams in a biomanufacturing facility?

Day Shift Upstream Manufacturing Associates frequently collaborate with downstream processing teams, quality control, and process engineering staff. Daily responsibilities often involve communicating batch progress, troubleshooting issues, and ensuring compliance with safety and GMP standards. Clear documentation and timely reporting to supervisors and quality teams are crucial for maintaining production flow. This cross-functional teamwork ensures efficient handoffs and rapid response to any process deviations, making collaboration a key part of the role.

What is the difference between Day Shift Upstream Manufacturing Associate vs Night Shift Upstream Manufacturing Associate?

AspectDay Shift Upstream Manufacturing AssociateNight Shift Upstream Manufacturing Associate
Work HoursTypically 8 AM - 4 PMTypically 8 PM - 4 AM
Work EnvironmentManufacturing floor during daytime operationsManufacturing floor during nighttime operations
Required SkillsSimilar technical skills, safety protocols, and certificationsSame technical skills, safety protocols, and certifications
Employer UsageCommonly used in biopharma and biotech manufacturingSame industry usage, different shift timing

The main difference between a Day Shift Upstream Manufacturing Associate and a Night Shift Upstream Manufacturing Associate lies in their working hours. Both roles require similar skills, certifications, and work environments, but they operate during different shifts. Employers in biopharma and biotech industries often employ both to ensure continuous production, with shift timing being the primary distinction.

What cities in Colorado are hiring for Day Shift Upstream Manufacturing Associate jobs?

Cities in Colorado with the most Day Shift Upstream Manufacturing Associate job openings:

Day Shift Upstream Manufacturing Associate jobs near you
Infographic showing various Day Shift Upstream Manufacturing Associate job openings in Colorado as of June 2026, with employment types broken down into 55% Full Time, 37% Part Time, 7% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Manufacturing Associate I/II

Boulder, CO

KBI Biopharma, Inc.
Biotechnology Research and Development • 1 - 5K employees

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

People enjoy working here

Respectful managers

Learn more about KBI Biopharma, Inc.external

$26.44 - $36.49/hr

Full-time

Posted 21 days ago

Job description

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: 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

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.

What KBI Biopharma employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply