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Biopharmaceutical Manufacturing Associate Jobs in San Ramon, CA

Astrix Inc

Sr. QC Associate

Fremont, CA · On-site

... biopharmaceutical manufacturing environment. * This role is responsible for executing and ... High School Diploma with 6+ years, Associate Degree with 4+ years, or Bachelor's Degree in a ...

Astrix Inc

QC Associate II

Fremont, CA · On-site

$30 - $35/hr

Pay Rate Low: 33 | Pay Rate High: 35 QC Associate II We are partnering with a multi-product biopharmaceutical manufacturing facility to place a QC Associate II within their Physical-Chemical Testing ...

Fladger Associates

QA Associate IV

Fremont, CA · On-site

Excellent employment opportunity for a QA Associate IV in the Fremont, CA area. * This position is ... Must be able to demonstrate understanding of biopharmaceutical manufacturing, technical equipment ...

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Biopharmaceutical Manufacturing Associate information

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$44

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for biopharmaceutical manufacturing associate in San Ramon, CA is $30.31, according to ZipRecruiter salary data. Most workers in this role earn between $25.77 and $35.48 per hour, depending on experience, location, and employer.

What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectBiopharmaceutical Manufacturing AssociateQuality Control Technician
Primary RoleSupports production processes, prepares materials, and ensures manufacturing runs smoothlyPerforms testing and inspection of products to ensure quality standards
Required SkillsKnowledge of GMP, aseptic techniques, and manufacturing proceduresLaboratory skills, attention to detail, knowledge of testing methods
Work EnvironmentCleanrooms, manufacturing floors, production facilitiesLaboratories, testing labs, quality control areas
CertificationsGMP training, sometimes cGMP certificationLab safety, GMP, and quality assurance training

The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.

What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?

Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.

What is a biopharmaceutical manufacturing associate?

As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.

What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?

To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.

What does a biopharmaceutical manufacturing associate do?

A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.
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What job categories do people searching Biopharmaceutical Manufacturing Associate jobs in San Ramon, CA look for? The top searched job categories for Biopharmaceutical Manufacturing Associate jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Biopharmaceutical Manufacturing Associate jobs? Cities near San Ramon, CA with the most Biopharmaceutical Manufacturing Associate job openings:
Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in San Ramon, CA as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $63,041 per year, or $30.3 per hour.

Cell Therapy Manufacturing Specialist

Kelly Services

South San Francisco, CA

Full-time, Other

Medical, Dental, Vision, Life, Retirement

Re-posted 17 days ago

Job description

Cell Therapy Manufacturing Associate
Multiple Positions
Location: South San Francisco, CA 94080
Company: Cell Therapy Manufacturing
Target Salary: $35-$40; BOE
Available Shifts
Day Shift
  • 7:00 AM – 7:30 PM | Sunday – Tuesday, alternating Wednesdays
  • 7:00 AM – 7:30 PM | Thursday – Saturday, alternating Wednesdays
Night Shift
  • 7:00 PM – 7:30 AM | Sunday – Tuesday, alternating Wednesdays
  • 7:00 PM – 7:30 AM | Thursday – Saturday, alternating Wednesdays
Initial Training Schedule
  • Monday – Friday, 9:00 AM – 5:30 PM
Position Summary
Seeking a highly motivated Cell Therapy Manufacturing Associate to support the development and production of advanced cell therapy products. This role will contribute to both GMP manufacturing operations and laboratory activities within a fast-paced, collaborative environment focused on advancing innovative therapies.
The ideal candidate is detail-oriented, committed to quality and compliance, and passionate about supporting cutting-edge biotechnology and cell therapy manufacturing.
Key Responsibilities
  • Execute manufacturing processes in both R&D and GMP environments following approved procedures, batch records, protocols, and SOPs.
  • Perform routine laboratory and manufacturing activities, including reagent preparation, leukopak processing, and sample testing.
  • Operate within a controlled GMP environment and perform cleanroom gowning according to established procedures.
  • Support process development efforts by providing operational feedback to engineering and process science teams.
  • Assist with process, equipment, and cleaning validation activities.
  • Contribute to the analysis, documentation, and presentation of technical results.
  • Perform routine laboratory and cleanroom maintenance, including cleaning, stocking, ordering supplies, and equipment qualification/maintenance.
  • Complete all required training and maintain compliance with internal policies, GMP requirements, and safety standards.
  • Prepare, review, revise, and maintain manufacturing documentation, including batch records, SOPs, protocols, and reports.
  • Initiate, investigate, and support the closure of deviations, CAPAs, and related quality documentation.
  • Review manufacturing records for accuracy and ensure timely submission of completed documentation.
  • Train and mentor new team members on manufacturing procedures, aseptic techniques, equipment operation, and troubleshooting.
  • Collaborate cross-functionally with Quality Assurance, Quality Control, Validation, Facilities, Materials Management, and other departments to support manufacturing objectives.
  • Perform additional duties as assigned.
Qualifications
Required
  • Bachelor’s degree, associate degree, technical diploma, or equivalent education in a scientific or related field.
  • Minimum 1 year of experience in biotechnology, biopharmaceutical manufacturing, or a related GMP-regulated environment.
  • Experience following SOPs, batch records, protocols, and GMP documentation requirements.
  • Strong attention to detail and commitment to quality, compliance, and safety.
  • Excellent communication, organizational, and interpersonal skills.
  • Strong analytical and problem-solving abilities.
Preferred
  • Experience in cell and gene therapy manufacturing.
  • Experience working in cGMP operations and cleanroom environments.
  • Familiarity with drug product manufacturing equipment and aseptic processing techniques.
Why Join our team?
You have the opportunity to work alongside talented scientists and manufacturing professionals developing transformative cell therapy technologies. We offer a collaborative environment where innovation, quality, and patient impact drive everything we do.
#P1
 
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.
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