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Day Shift Upstream Manufacturing Associate Jobs in San Ramon, CA

Millerknoll

Manufacturing Associate

San Francisco, CA · On-site

$20 - $22/hr

It's the ideal we strive toward each day in everything we do. Being a part of Holly Hunt means ... associates. This organization participates in E-Verify Employment Eligibility Verification. In ...

Alamar Biosciences

Senior Manufacturing Associate

Fremont, CA · On-site

$16.50 - $19.75/hr

Senior Manufacturing Associate handles various Manufacturing assignments ranging from routine to ... Second Shift Expectations: * Minimal supervision is provided over the weekend; candidates must ...

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All JobsDay Shift Upstream Manufacturing Associate JobsDay Shift Upstream Manufacturing Associate Jobs in San Ramon, CA

Day Shift Upstream Manufacturing Associate information

See San Ramon, CA salary details

$13

$23

$37

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

As of Aug 1, 2026, the average hourly pay for day shift upstream manufacturing associate in San Ramon, CA is $23.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $26.06 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.
What are popular job titles related to Day Shift Upstream Manufacturing Associate jobs in San Ramon, CA? For Day Shift Upstream Manufacturing Associate jobs in San Ramon, CA, the most frequently searched job titles are:
What job categories do people searching Day Shift Upstream Manufacturing Associate jobs in San Ramon, CA look for? The top searched job categories for Day Shift Upstream Manufacturing Associate jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities near San Ramon, CA 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 San Ramon, CA as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $48,435 per year, or $23.3 per hour.

Cell Therapy Manufacturing Associate

Kelly Services

South San Francisco, CA

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 9 days ago

Job description

Manufacturing Associate, Cell Therapy
Kelly® Science & Clinical is seeking a Manufacturing Associate for 6-month contract position with a national CDMO leader at their site in South San Francisco, CA.  If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Compensation: Day Shift: $35.00-38.00, Night Shift: $38.00-40.00
Schedule: 11PM - 7:30AM
  • week 1: sun, weds, thurs

           week 2: mon, tues, friday, sat

           It may shift to 12hr shifts for a project we are about to start.

Location: South San Francisco, CA
Duration: 6-month contract
SUMMARY
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to
join our Process Sciences team who will contribute significantly to the development and
manufacture of our advanced cell therapy manufacturing platform. The primary focus of this
position will be to support manufacturing operations, as well as day-to-day lab operations. This
is a hands-on position that will train in Process Development, Analytical Development, and/or
MSAT prior to joining the Manufacturing Group.
Candidates should enjoy working in a fast-paced, mission-driven environment, and be
prepared to tackle a broad selection of challenges as the company grows. 
RESPONSIBILITIES
  • Perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.)
  • Execute manufacturing processes in both an R&D and GMP environments, following protocols and/or standard operating procedures (SOPs)
  • Provide user feedback to engineering and process teams, support with requirements gathering and review
  • Support reagent preparation, leukopak processing, and sample testing in an R&D and GMP environment
  • Contribute to analysis and presentation of technical results at departmental meetings
  • Perform routine clean room and laboratory activities including ordering, cleaning, restocking, and equipment qualification/maintenance
  • Operate in a controlled GMP environment and perform gowning as per procedure
  • Complete required training and ensure compliance with established internal and external control procedures
  • Assist in the execution of process, equipment and cleaning validation
  • Responsible for revising and originating production records, standard operating procedures, protocols and reports
  • Initiate and support the closure of Deviation Reports and CAPAs
  • Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment and trouble-shooting skills
  • Review in-process and completed documents for accuracy and to make sure batch records are turned in to area management within specified days of completion
  • Work with Quality Control, Facilities, Materials Management, Quality Assurance and
  • Validation to complete assignments
  • Other duties as assigned

QUALIFICATIONS
  • Bachelor’s Degree or diploma in a scientific or related field is required
  • 1+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
  • Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries.
  • Must comply with the safety policies of the company and site
  • Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products
  • Proficiency in Drug Product-related process equipment
  • Must have experience following protocols, SOPs, and/or GMP documentation
  • Excellent verbal, written, presentation, and interpersonal skills
  • Strong analytical and problem-solving skills
  • Self-motivated and passionate about advancing the field of cell therapy
  • Self-awareness, integrity, authenticity, and a growth mindset
  • Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level
    P#1
    Send Resumes to Jacqueline.Sayoc@KellyScientific.com

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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