1

Quality Control Manager Jobs in San Ramon, CA (NOW HIRING)

Quality Control Inspector Location : San Ramon, CA Job Summary: We are seeking a Quality Control ... Support Quality Management System (QMS) and regulatory compliance requirements. * Assist with data ...

Document inspection and test results accurately and maintain detailed records of quality control ... Proficiency in using various measurement tools, testing equipment, and quality management software.

QC Lab Supervisor

Alameda, CA · On-site

$130K - $150K/yr

Oversee maintenance and calibration of laboratory equipment and manage lab supply inventory ... Author and revise QC SOPs, work instructions, protocols, and reports as needed. Qualifications

QC Lab Supervisor

Alameda, CA · On-site

$130K - $150K/yr

Oversee maintenance and calibration of laboratory equipment and manage lab supply inventory ... Author and revise QC SOPs, work instructions, protocols, and reports as needed. Qualifications

Inspector, Quality Control Location: San Ramon, California Duration: Contract Shift: Monday ... Follow Quality Management System (QMS) procedures and regulatory requirements Requirements: * High ...

Salary: $20 - $25 Quality Control Technician Who We Are Wisoman Foods Inc., located in Hayward, CA ... QA Manager. * Conduct pre-operational inspections of production equipment and facility prior to ...

QC Inspector

San Jose, CA · On-site

$26 - $28/hr

Bestronics, Inc has an exciting opportunity for QC Inspector to join its San Jose, CA team! At ... A safe and inclusive work environment with team and management support. * Paid on-site and off-site ...

Showing results 41-60

Quality Control Manager information

See San Ramon, CA salary details

$34.1K

$90.9K

$144.7K

How much do quality control manager jobs pay per year?

As of Aug 8, 2026, the average yearly pay for quality control manager in San Ramon, CA is $90,881.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,600.00 and $111,800.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

What is the difference between Quality Control Manager vs Quality Assurance Supervisor?

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

What are the key skills and qualifications needed to thrive as a quality control manager, and why are they important?

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.
What are the most commonly searched types of Quality Control jobs in San Ramon, CA? The most popular types of Quality Control jobs in San Ramon, CA are:
What job categories do people searching Quality Control Manager jobs in San Ramon, CA look for? The top searched job categories for Quality Control Manager jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Quality Control Manager jobs? Cities near San Ramon, CA with the most Quality Control Manager job openings:
Infographic showing various Quality Control Manager job openings in San Ramon, 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 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $90,881 per year, or $43.7 per hour.

QC Analyst II/III Reviewer (Contract)

Adverum Biotechnologies, Inc.

Redwood City, CA • On-site

$40 - $50/hr

Contractor

Re-posted 12 days ago


Job description

Adverum Biotechnologies, Inc., wholly owned subsidiary of Eli Lilly and Company, is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians' offices to eliminate the need for frequent ocular injections to treat these diseases. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.

Note to Recruiters and Agencies
All recruiter and agency inquiries must go through Adverum's internal Talent Acquisition team.  Unsolicited resumes sent to Adverum will be considered Adverum's property.   Adverum's Talent Acquisition team must expressly engage agencies for any requisition.  Direct contact with hiring managers by agencies will not be tolerated and may affect your ability to work with Adverum in the future.

Adverum is seeking a dedicated Quality Control Analyst to be a part of our vibrant team based in our Redwood City office. Reporting variably to the Quality Control Manager, Quality Control Lead, or as a part of a project hierarchy, this role will engage collaboratively with the QC team and other cross-functional teams. As a vital member of the Quality Control unit, the analyst will play a significant role in advancing and performing Quality Control (QC) review of different assay techniques, systems, policies, processes, procedures, and controls pertinent to the analytical examination of clinical materials. 

What You'll Do:
  • Perform QC review of release, stability, and in-process testing documentation and data to ensure compliance with GxP requirements. 

  • Review, analyze, and verify analytical data for drug substance and finished product testing, ensuring accuracy, completeness, reliability, and data integrity. 

  • Provide technical expertise in the review of analytical methods, assay execution, and troubleshooting activities within the QC laboratory, with particular focus on qPCR, Potency, ELISA, SEC and related techniques. 

  • Review and follow SOPs, test methods, specifications, and controlled documents; support the revision and continuous improvement of QC procedures to maintain compliance. 

  • Review completed testing records, sample documentation, and final result packages for release, stability, and in-process studies prior to approval. 

  • Identify, document, and own deviations through closure, including support for investigations, impact assessments, root cause analysis, and corrective actions as needed. 

  • Support qualification and validation activities through protocol and report review, documentation assessment, and verification of compliance with approved requirements. 

  • Support QC investigations, assay lifecycle activities, and nonclinical sample review as needed, collaborating cross-functionally to resolve quality and compliance issues. 

  • Provide guidance to junior staff, apply sound quality judgment in daily review activities, and communicate effectively with internal teams and external testing laboratories. 

About You :
  • Bachelor's degree in biology, chemistry, Biochemistry, or a related field, with a minimum of 3-5 years of experience (QC II) or 3-5 years' experience (QC III), preferable in a bio-pharma analytical laboratory setting 

  • Proficient in QC review of analytical documentation, including test records, data packages, instrument printouts, and associated documentation generated from systems such as Empower, SoftMax Pro and related laboratory software. 

  • Experience reviewing analytical methods, raw data, and supporting documentation for techniques such as Potency, qPCR, SEC, SDS-PAGE, DLS, and similar assays in a regulated laboratory environment. 

  • Experience in quality control documentation review is required based on level, with a strong understanding of compliance expectations, good documentation practices, and analytical record assessment; a solid foundation in molecular biology is desired. 

  • Experience with viral vector (adeno-associated virus) products is a plus. 

  • Must possess knowledge of cGMPs and regulatory prerequisites concerning the biotechnology and pharmaceutical sectors. 

  • Familiarity with statistical methods applicable to the analysis of experimental data. 

  • Proficiency in general and non-routine laboratory skills. 

  • Exceptional interpersonal, communication, and organizational skills are a must. 

  • Proficiency in MS Office and equipment-related software like Soft Max Pro is desired. 

$40 - $50 an hour
apply for this job