1

Day Shift Upstream Manufacturing Associate Jobs in California

Be Seen First

Upstream, Formulation & Downstream Manufacturing Associate Location: Tustin, CA Industry: Biopharmaceutical Manufacturing Schedule: Multiple Shifts Available Employment Type: Full-Time Position ...

Manufacturing Associate

Vacaville, CA ยท On-site

$25 - $28/hr

Onsite Shift: Thursday to Saturday and every other Wednesday from 06:00 AM to 07:00 PM Note: If ... Support Upstream Manufacturing activities, including media preparation, fermentation, harvest ...

New

next page

Showing results 1-20

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 California are hiring for Day Shift Upstream Manufacturing Associate jobs?

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

Infographic showing various Day Shift Upstream Manufacturing Associate job openings in California as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 23% Part Time, 2% Temporary, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Upstream, Formulation & Downstream Associate

Kinetic Personnel Group

Tustin, CA โ€ข On-site

$123/hr

Other

Posted 5 days ago


Job description

Upstream, Formulation & Downstream Manufacturing Associate Location: Tustin, CA Industry: Biopharmaceutical Manufacturing Schedule: Multiple Shifts Available Employment Type: Full-Time Position Summary A leading biopharmaceutical manufacturing company in Tustin, CA is seeking motivated Manufacturing Associates to support Upstream, Formulation, and Downstream manufacturing operations. These positions are responsible for executing manufacturing activities in a controlled GMP environment while following established procedures, safety requirements, and quality standards. Multiple shifts are available, including 1st, 2nd, and 3rd shifts. Candidates with a degree in Biology, Biochemistry, Biotechnology, Microbiology, or another related Life Science discipline are encouraged to apply. Key Responsibilities Upstream Manufacturing Support cell culture and upstream bioprocessing activities. Prepare and stage materials, equipment, and solutions for manufacturing operations. Assist with media and buffer preparation. Monitor and document manufacturing processes and equipment readings. Perform sampling and in-process testing as required. Follow SOPs, batch records, GMP requirements, and safety procedures. Maintain clean and organized manufacturing areas. Accurately document manufacturing activities in accordance with GMP requirements. Formulation Manufacturing Support formulation and preparation of biopharmaceutical products. Weigh, measure, and prepare raw materials and components according to approved procedures. Operate manufacturing equipment following established SOPs. Perform equipment setup, cleaning, and sanitization. Conduct in-process checks and sampling. Complete batch documentation and manufacturing records accurately. Follow aseptic and GMP practices as required. Downstream Manufacturing Support downstream purification and processing activities. Assist with filtration, chromatography, centrifugation, and related manufacturing processes. Prepare and stage materials and equipment for production. Monitor equipment and process parameters. Collect and document process samples. Perform equipment setup, cleaning, and sanitization. Follow SOPs, batch records, GMP requirements, and safety procedures. Qualifications Bachelor's degree in Biology, Biochemistry, Biotechnology, Microbiology, Chemistry, or another related Life Science discipline required. Manufacturing, laboratory, pharmaceutical, biotechnology, or biopharmaceutical experience preferred. Understanding of basic biological and laboratory principles. Ability to accurately follow written procedures and SOPs. Strong attention to detail and documentation skills. Ability to work effectively in a team-oriented manufacturing environment. Ability to work multiple shifts, including evenings, nights, weekends, or overtime as required. Ability to work in a controlled/GMP manufacturing environment. Strong communication and organizational skills. Ability to learn manufacturing equipment, processes, and procedures quickly. Preferred Experience GMP or cGMP experience. Biopharmaceutical or pharmaceutical manufacturing experience. Cell culture or upstream processing experience. Formulation or solution preparation experience. Downstream purification experience. Experience with batch records and manufacturing documentation. Experience working in a cleanroom or controlled manufacturing environment. Physical Requirements Ability to stand and walk for extended periods. Ability to wear required PPE and cleanroom garments. Ability to lift and move materials and equipment as required. Ability to perform repetitive manufacturing activities. Ability to work in a controlled manufacturing environment. Why Join Us? This is an excellent opportunity for a Life Science graduate to build hands-on experience in biopharmaceutical manufacturing and develop expertise across Upstream, Formulation, or Downstream processing. Successful candidates will work in a regulated GMP environment supporting the production of high-quality biopharmaceutical products. Multiple shifts available. Apply today for immediate consideration. Pay: $20-$21 KPG123