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Quality Assurance Biotech Jobs in Riverside, CA (NOW HIRING)

... biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team ... A minimum of three to five (3-5) years administration experience in a Quality Assurance Document ...

... biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team ... A minimum of three to five (3-5) years administration experience in a Quality Assurance Document ...

... or biotechnology organization. They will possess deep expertise in talent management ... Quality Assurance & Regulatory Compliance * Partner closely with Quality/Regulatory to uphold and ...

... or biotechnology organization. They will possess deep expertise in talent management ... Quality Assurance & Regulatory Compliance Partner closely with Quality/Regulatory to uphold and ...

... or biotechnology organization. They will possess deep expertise in talent management ... Quality Assurance & Regulatory Compliance Partner closely with Quality/Regulatory to uphold and ...

... or biotechnology organization. They will possess deep expertise in talent management ... Quality Assurance & Regulatory Compliance * Partner closely with Quality/Regulatory to uphold and ...

... Quality Assurance, Human Resources to develop plans to meet business objectives - Lift up to 49 ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

... Quality Assurance, Human Resources to develop plans to meet business objectives * Lift up to 49 ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

... Quality Assurance, Human Resources to develop plans to meet business objectives - Lift up to 49 ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

... Quality Assurance, Human Resources to develop plans to meet business objectives - Lift up to 49 ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

... Quality Assurance, Human Resources to develop plans to meet business objectives - Lift up to 49 ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Showing results 41-60

Quality Assurance Biotech information

See Riverside, CA salary details

$13

$30

$64

How much do quality assurance biotech jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for quality assurance biotech in Riverside, CA is $30.56, according to ZipRecruiter salary data. Most workers in this role earn between $19.57 and $35.87 per hour, depending on experience, location, and employer.

What is a quality assurance biotech?

A Quality Assurance (QA) Biotech job involves ensuring that biotechnology products meet regulatory and company standards for safety, efficacy, and quality. QA professionals develop and implement quality systems, conduct audits, review documentation, and ensure compliance with Good Manufacturing Practices (GMP) and other regulations. They collaborate with various departments, including manufacturing, R&D, and regulatory affairs, to maintain product integrity. Their role is critical in preventing defects, ensuring consistent processes, and maintaining compliance with industry standards.

What are the key skills and qualifications needed to thrive in quality assurance biotech?

To thrive as a Quality Assurance Biotech, you need a solid understanding of biotechnology processes, quality control methodologies, and regulatory standards such as GMP, often supported by a degree in biology, chemistry, or a related field. Familiarity with laboratory information management systems (LIMS), documentation software, and industry certifications like ASQ or GMP training is highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills are valued soft skills in this role. These abilities ensure precise compliance with regulatory requirements, facilitate collaboration with cross-functional teams, and help maintain the integrity and safety of biotech products.

What are the most common challenges faced by quality assurance professionals in the biotech industry?

Quality Assurance professionals in biotechnology often encounter challenges related to staying up-to-date with evolving regulatory requirements and ensuring that all processes consistently meet strict quality standards. Additionally, managing thorough documentation and collaborating across various departments—such as research, manufacturing, and regulatory affairs—can be complex. Those in the role may also need to respond quickly to deviations or quality events, requiring both proactive problem-solving and excellent organizational skills. However, overcoming these challenges is highly rewarding, as it directly contributes to maintaining the safety and efficacy of biotech products.

What are the most commonly searched types of Quality Assurance Biotech jobs in Riverside, CA?

The most popular types of Quality Assurance Biotech jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Quality Assurance Biotech jobs?

Cities near Riverside, CA with the most Quality Assurance Biotech job openings:

Infographic showing various Quality Assurance Biotech job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $63,561 per year, or $30.6 per hour.

Document Control Labeling Spec

Santa Ana, CA

$31.11 - $38/hr

Full-time

Medical, Dental

Posted 4 days ago


Job description

Position OverviewWe are hiring a Document Control Labeling Specialist. The Document Control Labeling Specialist will compile and maintain control records relating to label issuance, print of production labels for manufacturing, assemble batch records (DHR) for all production departments and verify all documents including formulations, manufacturing protocols and Bill of Materials prior to lot folder assembly. They also will maintain label inventory, word processing of controlled documents and support the Document Control program.Shift: 5am - 1:30pmCompany OverviewAt FUJIFILM Biosciences, we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges.Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Biosciences.Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide.Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careersJob DescriptionResponsibilities:Compile and maintain control records relating to label issuance. Printing production labels for manufacturing (managing work schedules)Assembly of Lot Folders for all departments (managing work schedules)Verification of all documents prior to lot folder assemblyMaintain inventory of all label and ribbon stocksSupport document control program. Required Skills/Education: High school diploma or equivalent.A minimum of three to five (3-5) years administration experience in a Quality Assurance Document Control medical device manufacturing environment or equivalent.Experience with Labeling Systems.Computer skills, specifically MS Word, Excel, GMailGraphic design knowledge a plus.Current industry regulations, e.g. cGMP, ISO 13485, Code of Federal Regulations, MDD 93/42/EEC, IVDD 98/79/EC, TGA, and Canadian Medical Device RegulationAbility to speak, write, and read English. Good oral and written communication skillsSalary and Benefits:For California, the base salary range for this position is $31.11 - $38 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.).Medical, Dental, VisionLife Insurance401kPaid Time Off*#LI-onsiteEEO InformationFujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.ADA InformationIf you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (flbi@fujifilm.com). Salary: . Date posted: 08/26/2026