ZipRecruiter

Log In

1

Day Shift Upstream Manufacturing Associate Jobs (NOW HIRING)

Kinetic Personnel Group

Be Seen First

Manufacturing Associate Biopharma

Tustin, CA · On-site

$20 - $21/hr

Upstream Manufacturing Associate Position Summary We are seeking a motivated Upstream Manufacturing Associate to join our biopharmaceutical manufacturing team. This entry-level position supports the ...

Kinetic Personnel Group

Be Seen First

Manufacturing Associate Biopharma

Tustin, CA · On-site

$20 - $21/hr

Upstream Manufacturing Associate Position Summary We are seeking a motivated Upstream Manufacturing Associate to join our biopharmaceutical manufacturing team. This entry-level position supports the ...

Evotec

Manufacturing Associate I

Redmond, WA · On-site

$26 - $30/hr

Days, Sun to Wed 7am till 6pm - Upstream Manufacturing About Us: At Just Evotec Biologics, we ... Day shift- Sun to Wed 0700-1800 What You'll Do: * Perform and monitor critical processes (i.e ...

Evotecgroup

Manufacturing Associate I

Redmond, WA · On-site

$26 - $30/hr

Days, Sun to Wed 7am till 6pm - Upstream Manufacturing About Us: At Just Evotec Biologics, we ... Day shift- Sun to Wed 0700-1800 What You'll Do: * Perform and monitor critical processes (i.e ...

next page

Showing results 1-20

All JobsDay Shift Upstream Manufacturing Associate Jobs

Day Shift Upstream Manufacturing Associate information

See salary details

$12

$20

$33

How much do day shift upstream manufacturing associate jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for day shift upstream manufacturing associate in the United States is $20.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 per hour, depending on experience, location, and employer.

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 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 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 are the key skills and qualifications needed to thrive as a Day Shift Upstream Manufacturing Associate, and why are they important?

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.
More about Day Shift Upstream Manufacturing Associate jobs
What cities are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities with the most Day Shift Upstream Manufacturing Associate job openings:
What states have the most Day Shift Upstream Manufacturing Associate jobs? States with the most job openings for Day Shift Upstream Manufacturing Associate jobs include:
What job categories do people searching Day Shift Upstream Manufacturing Associate jobs look for? The top searched job categories for Day Shift Upstream Manufacturing Associate jobs are:
Day Shift Upstream Manufacturing Associate jobs near you
Infographic showing various Day Shift Upstream Manufacturing Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $43,341 per year, or $20.8 per hour.
Upstream Manufacturing Associate

Upstream Manufacturing Associate

Kinetic Personnel Group

Tustin, CA • On-site

Other

Posted 5 days ago

Job description

Upstream Manufacturing Associate Position Summary We are seeking a motivated Upstream Manufacturing Associate to join our biopharmaceutical manufacturing team. This entry-level position supports the production of biologic drug substances through upstream manufacturing processes in a cGMP-regulated environment. The ideal candidate is a recent graduate with a strong scientific background who is eager to begin a career in biopharmaceutical manufacturing. Key Responsibilities Perform upstream manufacturing activities including media and buffer preparation, cell culture support, and bioreactor operations. Execute manufacturing processes according to batch records, standard operating procedures (SOPs), and cGMP requirements. Operate, monitor, clean, and maintain manufacturing equipment and process systems. Accurately complete batch records and manufacturing documentation in accordance with Good Documentation Practices (GDP). Monitor critical process parameters and report any deviations or equipment issues. Assist with equipment setup, sanitization, and routine maintenance activities. Maintain a clean and organized manufacturing environment while following safety and contamination control procedures. Collaborate with Manufacturing, Quality Assurance, Quality Control, and Engineering teams to support production goals. Participate in training programs and continuously develop technical knowledge of upstream bioprocessing. Minimum Qualifications Bachelor's degree required in Biology, Chemistry, Biochemistry, or a closely related Life Science discipline. No prior industry experience required. Recent graduates are encouraged to apply. Basic understanding of cell biology, microbiology, biochemistry, or laboratory techniques gained through coursework or academic laboratory experience. Strong attention to detail and ability to follow written procedures. Excellent communication and teamwork skills. Ability to work in a fast-paced, regulated manufacturing environment. Basic computer proficiency, including Microsoft Office. Preferred Qualifications Academic laboratory experience with cell culture, microbiology, or biochemistry. Knowledge of cGMP, aseptic techniques, or biopharmaceutical manufacturing principles through coursework or internships. Experience using laboratory equipment such as balances, pH meters, pipettes, or analytical instruments. Physical Requirements Ability to stand for extended periods during manufacturing operations. Ability to lift up to 35 pounds. Ability to wear required personal protective equipment (PPE), including cleanroom gowning. Ability to work flexible schedules, including weekends or holidays, as production needs require. KPG123

Apply