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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 ...

Fladger Associates

Batch Record Coordinator

Fremont, CA · On-site

$21.25 - $29/hr

This position requires intermediate understanding of Biopharmaceutical Manufacturing, especially in the use of Batch Records. * Requires strong organizational skills and advanced interpersonal skills.

Fladger Associates

Batch Record Coordinator

Fremont, CA · On-site

$21.25 - $29/hr

This position requires intermediate understanding of Biopharmaceutical Manufacturing, especially in the use of Batch Records. * Requires strong organizational skills and advanced interpersonal skills.

Fladger Associates

Batch Record Coordinator

Fremont, CA · On-site

$21.25 - $29/hr

This position requires intermediate understanding of Biopharmaceutical Manufacturing, especially in the use of Batch Records. * Requires strong organizational skills and advanced interpersonal skills.

Astrix Inc

QC Associate II

Fremont, CA · On-site

$30 - $33/hr

Pay Rate Low: 30 | Pay Rate High: 33 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 ...

Cytokinetics

Associate Scientist

South San Francisco, CA · On-site

$121K - $141K/yr

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years ... Working knowledge of oral solid dosage form development, pharmaceutical manufacturing, and product ...

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Biopharmaceutical Manufacturing Associate information

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How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 29, 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 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 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.

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 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 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.

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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.

Sr. QC Associate

Astrix Inc

Fremont, CA • On-site

Full-time

Re-posted 10 days ago

Job description

Pay Rate Low: 32 | Pay Rate High: 34
Our client is a global, research-driven pharmaceutical manufacturer focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Sr. QC Associate to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference!
Title: Sr. Quality Control Associate (Contract)
Location: Alameda County, CA
Schedule & Contract
  • Contract Duration: 3 months (Likely to extend)
  • Schedule: Monday-Friday, 8:00 AM-5:00 PM
  • Hours: 40 hours per week

Job Duties
We are seeking a Quality Control Analyst to support analytical testing activities within a cGMP-regulated biopharmaceutical manufacturing environment.
  • This role is responsible for executing and coordinating analytical testing of bulk drug substance and drug product across multiple analytical platforms, including chromatography, potency/bioassays, microbiology, raw materials, cleaning validation, and packaging testing.
  • The analyst will independently perform and review 3-5 analytical methods, ensure accurate documentation, and support data trending, investigations, and compliance activities.
  • Responsibilities include authoring and maintaining QC documentation (SOPs, test methods, specifications, and reports), identifying process improvements, and ensuring adherence to global regulatory requirements (e.g., FDA, EMA).

Qualifications
  • High School Diploma with 6+ years, Associate Degree with 4+ years, or Bachelor's Degree in a science or engineering field with 2+ years of cGMP experience
  • Prior Quality Control experience preferred
  • Strong technical knowledge of analytical testing in biopharmaceutical manufacturing
  • Demonstrated ability to independently execute methods, review data, and ensure compliance.

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