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Quality Control Analyst Jobs in Santa Rosa, CA (NOW HIRING)

Socket.dev

Sr Supplier QA Engineer

Healdsburg, CA · On-site

$101.15 - $136.85/hr

Performance Analysis. Quality Audit. Quality Control/Testing. Quality Improvement. Quality Inspection. Supplier Management. Vendor Relationships and evaluation. Physical Requirements * Must be able ...

New

Kavaliro

Quality Technician (Swing)

Santa Rosa, CA · On-site

$19.75 - $26.50/hr

Working within the designated area of expertise, the candidate will clarify, analyze, develop, and ... in quality control within manufacturing environment. Kavaliro provides Equal Employment ...

Straus Family Creamery

Quality Technician

Rohnert Park, CA · On-site

$22 - $24/hr

Submit daily Analytical and Micro samples to QC for appropriate testing * Provide continuous and consistent quality leadership to production operators, looking for ways to improve product quality and ...

Straus Family Creamery

Quality Technician

Rohnert Park, CA · On-site

$22 - $24/hr

Submit daily Analytical and Micro samples to QC for appropriate testing * Provide continuous and consistent quality leadership to production operators, looking for ways to improve product quality and ...

Abbott

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

... control, management review, and quality metrics. * Conducts complex analysis of quality records, laboratory data, audit findings, investigations, trends, and reports to identify opportunities for ...

Abbott

Quality Engineer

Santa Rosa, CA

$78K - $101K/yr

... control, management review, and quality metrics. * Conducts complex analysis of quality records, laboratory data, audit findings, investigations, trends, and reports to identify opportunities for ...

Abbott

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

... control, management review, and quality metrics. * Conducts complex analysis of quality records, laboratory data, audit findings, investigations, trends, and reports to identify opportunities for ...

Rack and Riddle

Lab Lead

Healdsburg, CA · On-site

$26 - $28/hr

This role combines hands-on analytical chemistry and microbiology with critical thinking to support root cause investigations. Acting as a key bridge between the lab, cellar, QC and bottling lines ...

Apple

Control Systems Engineer

Bodega Bay, CA

$184K - $324K/yr

... quality over a wide range of use cases and component variation. Past projects have addressed ... level analysis and modeling of control systems, developing robust control strategies, guiding ...

Tekberry

Quality Engineer Specialist

Santa Rosa, CA · On-site

$31 - $39/hr

Analyze manufacturing, coating, inspection, testing, and SPC data to identify trends and recommend ... Any job offer may be contingent upon the applicant's ability to meet applicable export control ...

TEKBERRY

Quality Engineering Specialist

Santa Rosa, CA · On-site

$31 - $39/hr

Analyze manufacturing, coating, inspection, testing, and SPC data to identify trends and recommend ... Any job offer may be contingent upon the applicant's ability to meet applicable export control ...

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All JobsQuality Control Analyst JobsQuality Control Analyst Jobs in Santa Rosa, CA

Quality Control Analyst information

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How much do quality control analyst jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for quality control analyst in Santa Rosa, CA is $30.52, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $33.89 per hour, depending on experience, location, and employer.

What is a quality control analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

What are the key skills and qualifications needed to thrive as a quality control analyst?

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by quality control analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

How much does a quality control analyst earn?

The average salary for a quality control analyst typically ranges from $45,000 to $70,000 per year, depending on experience, industry, and location. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. Many roles also include benefits such as health insurance and paid time off.
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Cities near Santa Rosa, CA with the most Quality Control Analyst job openings:

Quality Control Analyst jobs near you
Infographic showing various Quality Control Analyst job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 5% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $63,485 per year, or $30.5 per hour.

Research Associate 1, Analytical Services

BIOMARIN PHARMACEUTICAL

Novato, CA • On-site

Full-time

Re-posted 6 days ago

BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

About Technical Operations
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.

Research Associate, Analytical Services
JOB DESCRIPTION
Research Associate is an onsite laboratory position. The selected candidate will work in the Analytical Services team, under the Analytical Sciences group to assist in the advancement of BioMarin's therapeutics for clinical evaluation and potential commercialization. The selected candidate will be responsible for applying technical expertise to the execution of laboratory activities related to GxP and non-GxP testing of early clinical programs and their transition to late stage, commercial and post-commercialization.
Under limited supervision, the candidate will ensure phase-appropriate performance, troubleshooting, optimization, qualification, validation, and transfer of methods for testing pharmaceutical drug substance and drug product. In addition, this role will support training for site QC / Global QC / Contract Test Labs / In-Country Testing Laboratories personnel in new techniques and methods. The selected candidate should possess excellent analytical, organizational and communication skills and be a self-starter willing to work efficiently and collaboratively in a dynamic environment.
RESPONSIBILITIES
Responsibilities include, but are not limited to the following:
Method Qualification, Validation, Transfer and Optimization
Lead and/or perform analytical testing such as HPLC/UPLC, Electrophoresis, UV Spectrophotometry, plate-based assays including ELISAs and cell-based Bioassays, Nucleic Acid Analysis and compendial physicochemical assays.
Draft and review documents such as, analytical procedures, method validation protocols/reports, experimental designs, verification, and transfer protocols/reports
Manage and perform activities associated with validation and transfer of QC Methods used to support BioMarin's in-process, release and stability testing programs to internal laboratories, CTOs, In-Country Test Laboratories and other strategic partners
Lead/support and document escalated laboratory investigations to identify the root cause and to establish effective corrective and preventative actions with minimal delay
Provide technical expertise for analytical test methods (optimize, validate, and troubleshoot) to stakeholders in QC, Drug Substance and Drug Product Technology teams
Support the maintenance of method and analytical equipment performance
Trend, analyze and interpret analytical results.
Conduct data review and sign-off in applicable document and data management systems
Support the performance of project management functions such as: ensuring adherence to timelines, mobilizing stakeholders, prioritization of work efforts, understanding and applying escalation process
Regulatory Compliance, Audit and Site Support
Lead/support the effort to maintain the laboratory in an inspection-ready state including support of equipment management (e.g., check reference materials for expiration, etc.)
Support efforts to provide technical support to regulatory agency inspections and audits (e.g. Pre-Licensing Inspection (PLI) and periodic cGMP inspections)
General understand and application of USP, EP, JP and ICH regulatory guidelines and directives
Cross-Functional Support
Provide laboratory support to Manufacturing, Quality and QC during manufacturing and/or QC investigations
Liaise with Analytical Product Leads, Drug Substance and Drug Product Technology Teams, Manufacturing, Quality Control to support GxP testing
Process Improvement and Training
Act as technical resource (SME) to train other Analysts in areas of expertise
Support or lead continuous improvement in laboratory operations (procedures and systems) to improve organizational effectiveness and phase-appropriate testing compliance.
Required Skills:
Experience in performing one or more combinations of analytical methods including HPLC/UPLC, Electrophoresis, UV Spectrophotometry, plate-based assays including ELISAs and cell-based Bioassays, Nucleic Acid Analysis and compendial physicochemical assays Experience or understanding of GMP/GLP requirements.
Ability to analyze and interpret data.
Good written and oral communication skills, with the ability to communicate complex information.
Strong organizational skills with the ability to effectively multi-task and prioritize.
Proven flexibility and execution skills to deliver in a fast-paced, multi-tasking environment.
Desired Skills:
Experienced in method development, qualification, and transfer.
Knowledge of biopharmaceutical development is a plus.
Experience working in a cross-functional environment.
Primarily a laboratory position; contact with chemicals that may be hazardous is part of routine activities. The employee will be trained to use common laboratory equipment and minimize exposure to hazards. Desktop or laptop computer work is also a major component of the job. This is a fully onsite role. The position may require occasional non-routine work hours support.
Education
Bachelor's/ in Chemistry, Biochemistry, Analytical Chemistry, or a related field with at least 2- 4 years of experience in a Biologics or Pharmaceutical environment.
A Master's Degree in a related field is desirable, but not required.

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.

Employment Type: Fulltime-Regular

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