ZipRecruiter

Log In

1

Day Shift Upstream Manufacturing Associate Jobs in Santa Rosa, CA

TEKBERRY

Manufacturing Associate

Santa Rosa, CA · On-site

$28/hr

Day Shift, Monday-Friday Location: Santa Rosa, CA Job Code: JPC-12494 Tekberry is looking for a highly qualified and motivated Manufacturing Associate to work on-site with our client, a top-tier ...

Tekberry

Manufacturing Associate

Santa Rosa, CA · On-site

$28/hr

Day Shift, Monday-Friday Location: Santa Rosa, CA Job Code: JPC-12494 Tekberry is looking for a highly qualified and motivated Manufacturing Associate to work on-site with our client, a top-tier ...

Kelly Services

Manufacturing Associate

Novato, CA

$28 - $32.20/hr

... Manufacturing Associate at Kelly Services: Kelly Benefit Offerings Through EnrollVB: This is your ... Flexibility to work any assigned shift (days/nights, weekends, holidays, and overtime as needed)

next page

Showing results 1-20

All JobsDay Shift Upstream Manufacturing Associate JobsDay Shift Upstream Manufacturing Associate Jobs in Santa Rosa, CA

Day Shift Upstream Manufacturing Associate information

See Santa Rosa, CA salary details

$13

$22

$36

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

As of Aug 2, 2026, the average hourly pay for day shift upstream manufacturing associate in Santa Rosa, CA is $22.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $25.48 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 Santa Rosa, CA? For Day Shift Upstream Manufacturing Associate jobs in Santa Rosa, CA, the most frequently searched job titles are:
What job categories do people searching Day Shift Upstream Manufacturing Associate jobs in Santa Rosa, CA look for? The top searched job categories for Day Shift Upstream Manufacturing Associate jobs in Santa Rosa, CA are:
What cities near Santa Rosa, CA are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities near Santa Rosa, 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 Santa Rosa, CA as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 25% Part Time, 1% Temporary, and 3% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $47,386 per year, or $22.8 per hour.

Associate, Manufacturing (Day Shift)

BIOMARIN PHARMACEUTICAL

Novato, CA • On-site

Full-time

Re-posted 27 days ago

BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

51st of 86 rated pharmaceutical

Job description

Who We Are
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
SUMMARY
BioMarin's Novato commercial manufacturing operations produce a variety of therapies using perfusion/fermentation based cell culture processes and multiple column purification systems. Under direction of the Supervisor, the Manufacturing Associate will be responsible for job functions that support activities for commercial manufacturing. The Associate is responsible for working on a shift with 6 - 10 peers with responsibilities of preparing large scale solutions (buffers and media), managing raw material inventory, or operating process equipment in Upstream or Downstream areas while supporting daily operations. Additional responsibilities include ensuring compliance with current Good Manufacturing Practice regulations (cGMP), Standard Operating Procedures (SOPs), product licenses, corporate policies and safety practices. The position will require shift work and potentially including weekends, off hours and holidays.
RESPONSIBILITIES
-Operate large scale bioprocess equipment for the Cell Culture, Purification or Buffer and Media processing
-Perform all aspects of processing with a broad understanding of science, compliance, and technical aspect
-Display competency with process equipment and automated control systems
-Perform cleaning and sterilization of parts and equipment used with manufacturing process
-Knowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.
-Ability to understand, apply, and evaluate basic chemistry, biology and scientific principles as appropriate for the position
-Proficiency with compliance; adherence to standard operating procedures, batch record, good documentation practices and data capturing
EDUCATION
-Bachelor's degree in science related area or engineering or Associate's degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry
WORK ENVIRONMENT/PHYSICAL DEMANDS
-Consists of strenuous, repetitive work. The following list of physical movements maybe used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands.
-Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds.
-May require work around loud equipment.
-The use of personal protective equipment will be required.
-Requires various shift based work and off hours

Shift Details: Thurs-Sat 0600-1900 with alternating Wed.


We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Employment Type: Fulltime-Regular

What BioMarin Pharmaceutical employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply