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Manager Qc Jobs in California (NOW HIRING)

Dycom Industries, Inc.

Manager Quality Control

Upland, CA · On-site

$90K - $115K/yr

We are looking for a Manager of Quality Control Field who is passionate about building "boots on the ground" excellence and mentoring the next generation of industry experts. Join a team that ...

CEMEX

Manager Quality Control Aggregates

Rialto, CA · On-site

Provide leadership, direction, coaching, mentoring, performance management, and professional development for Quality Control personnel, including technicians and supervisors, while fostering a ...

CEMEX

Manager Quality Control Aggregates

Rialto, CA · On-site

Provide leadership, direction, coaching, mentoring, performance management, and professional development for Quality Control personnel, including technicians and supervisors, while fostering a ...

Gilead

Senior Manager, Quality Control

La Verne, CA · On-site

Manages QC personnel, including organizing and prioritizing daily tasks, performing training, and writing performance reviews. * Oversees overall day-to-day operation of laboratories. * Attends ...

Constellation Brands

Quality Control Manager

Sonoma, CA · On-site

$100K - $153K/yr

Position Summary The Manager, Quality Control provides leadership for production quality, continuous improvement, quality investigations, and supplier support across the network of wineries and ...

Sunbit

Sr. Manager, Quality Control

Los Angeles, CA · On-site +1

Description JOB TITLE: Sr. Manager, Quality Control LOCATION: Los Angeles, CA (Hybrid in our Westwood Office, 3 days/ week) REPORTS TO: Head of Data The Company Sunbit builds financial technology for ...

Bachem

Manager / Sr. Manager, Quality Control

Vista, CA · On-site

$133K - $183K/yr

A brief overview The Manager / Sr. Manager, Quality Control fulfills a critical role in the active pharmaceutical ingredient (API) manufacturing operations. This individual is responsible for ...

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Manager Qc information

See California salary details

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$85K

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How much do manager qc jobs pay per year?

As of Aug 30, 2026, the average yearly pay for manager qc in California is $85,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,400.00 and $134,200.00 per year, depending on experience, location, and employer.

What are the responsibilities of a Manager QC?

A Manager QC (Quality Control Manager) is responsible for overseeing the quality assurance processes within a company to ensure that products meet required standards and specifications. They develop and implement quality control procedures, supervise QC staff, conduct audits, and analyze quality data to identify areas for improvement. Additionally, they collaborate with other departments to resolve quality issues and ensure compliance with industry regulations. Their ultimate goal is to maintain consistent product quality and customer satisfaction.

What skills and qualifications are needed to thrive as a Manager QC?

To thrive as a Manager QC (Quality Control), you need a solid background in quality assurance processes, analytical testing, and industry regulations, typically supported by a degree in science or engineering. Familiarity with quality management systems (like ISO standards), statistical analysis software, and certification such as Six Sigma or ASQ is often required. Strong leadership, problem-solving, and communication skills help drive team performance and handle complex quality issues. These skills are essential for maintaining product standards, ensuring regulatory compliance, and supporting continuous improvement within the organization.

What challenges does a Manager QC face when balancing regulatory compliance with production timelines?

A Manager QC (Quality Control) often faces the challenge of ensuring that all products meet strict regulatory standards while also supporting the company's production goals. This balancing act requires effective communication with production and regulatory teams, as well as proactive planning to anticipate potential bottlenecks. Managers must remain vigilant about documentation and testing, and be prepared to address unforeseen quality issues without causing significant delays. Success hinges on strong leadership, a detail-oriented mindset, and the ability to adapt quickly to changing priorities.

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

AspectManager QcQuality Assurance Supervisor
ResponsibilitiesOversees quality control processes, manages teams, implements quality policiesSupervises QA team, conducts inspections, ensures compliance with standards
CredentialsBachelor's degree in related field, experience in quality management, certifications like CQEBachelor's degree, experience in quality assurance, certifications like CQE or ASQ certifications
Work EnvironmentManagement level, strategic planning, cross-department collaborationOperational level, hands-on inspections, team supervision
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, electronics, consumer goods

The main difference between a Manager Qc and a Quality Assurance Supervisor lies in scope and level of responsibility. The Manager Qc typically handles strategic oversight and manages multiple teams, while the QA Supervisor focuses on daily supervision and operational tasks. Both roles require similar credentials and are vital in quality management across industries.

Is manager QC a high paying job?

Manager QC roles typically offer higher salaries compared to entry-level quality control positions, with pay varying based on industry, experience, and location. These roles often require strong leadership, technical skills, and certifications, and they tend to be well-compensated in manufacturing, pharmaceuticals, and food industries.

What does a manager QC do?

A manager QC (Quality Control) oversees the inspection and testing of products or processes to ensure they meet quality standards. They develop quality procedures, supervise QC staff, analyze data, and implement improvements to maintain product integrity and compliance with industry regulations.

What are the most commonly searched types of Qc jobs in California?

The most popular types of Qc jobs in California are:

What cities in California are hiring for Manager Qc jobs?

Cities in California with the most Manager Qc job openings:

Manager Qc jobs near you
Infographic showing various Manager Qc job openings in California as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $85,031 per year, or $40.9 per hour.

Manager, Quality Control

Carlsbad, CA • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

170th of 545 rated manufacturers

People enjoy working here

Good employer

Recommended by students

Learn more about Thermo Fisher Scientificexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago

Job description

Work Schedule
First Shift (Days)
Environmental Conditions
Office
Job Description
Location/Division Specific Information
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day by enabling our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges.
The Manager, QC supports the Biosciences Division and is based at our Carlsbad, CA site. This role reports directly to the Director, Quality.
  • This is a fully onsite position. Unfortunately, relocation assistance is NOT provided. Priority will be given to LOCAL candidates currently residing in Southern California.
  • Must be legally authorized to work in the United States without sponsorship now or in the future.
  • Must be able to pass a comprehensive background check, which includes a drug screen.

DESCRIPTION
How will you make an impact?
The Manager, QC provides leadership and operational oversight for Quality Control laboratory operations supporting multiple product lines manufactured at the Carlsbad site. This role leads and develops the QC laboratory team, ensuring effective analytical and release testing, regulatory compliance, and reliable laboratory execution while maintaining a culture of quality, data integrity, and continuous improvement.
As a QC leader for the site, the Manager partners closely with Operations, Manufacturing Sciences, Quality Systems & Compliance, Regulatory Affairs, R&D, and other key stakeholders to ensure product quality, resolve laboratory and testing issues, and support business objectives. Through sound scientific judgment, data-driven decision making, and cross-functional collaboration, this role advances product quality, laboratory performance, customer outcomes, and operational excellence.
What will you do?
  • Lead, develop, and manage the QC laboratory team, including supervisors and team leads, ensuring effective laboratory operations, building team capability, and driving consistent execution of quality control and testing priorities across multiple product lines.

  • Oversee analytical testing operations, including in-process and finished product release testing, troubleshooting investigations, and support for method validation, qualification, and transfer activities, ensuring timely execution and compliance with established methods, specifications, and quality standards.

  • Strategically manage laboratory capacity, testing priorities, financials, productivity, and resource allocation to meet manufacturing and business needs while maintaining quality standards and compliance.

  • Leverage laboratory performance data and quality trends, including out-of-specification (OOS) results, laboratory deviations, and testing metrics, to identify risks and opportunities, drive deeper investigation when warranted, and partner with cross-functional teams to improve product quality, laboratory performance, and customer outcomes.

  • Drive effective QC execution of deviation investigations, change controls, and laboratory-related nonconformance records, ensuring timely progression, thorough root cause analysis, effective resolution, and high-quality documentation in alignment with Quality Systems & Compliance requirements.

  • Ensure QC laboratory operations and practices align with applicable cGMP, ISO, Quality Management System, and regulatory requirements, maintaining inspection and audit readiness and partnering with Quality Systems & Compliance and Regulatory Affairs to identify and address laboratory quality or compliance gaps.

  • Provide QC leadership for significant laboratory decisions and analytical activities supporting material disposition and participate as a subject matter expert in site governance forums, including CAPA Review Board, Change Control Review Board, and other cross-functional quality forums, as appropriate.

  • Partner with Operations, Manufacturing Sciences, Quality Systems & Compliance, Regulatory Affairs, R&D, and other key stakeholders to resolve significant product and process quality issues related to analytical testing and drive effective, sustainable solutions.

  • Champion Practical Process Improvement (PPI) and continuous improvement within the laboratory, using QC insight and cross-functional influence to strengthen analytical testing, laboratory efficiency, product quality, and a culture of quality and accountability.

  • Maintain strong alignment with divisional, group, and corporate Quality and Regulatory Affairs organizations to ensure QC laboratory priorities and execution support broader Quality and business objectives.

REQUIREMENTS
How will you get here?
Education
  • Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related scientific field required.

  • Advanced degree in a technical or business discipline preferred.

Experience
  • Minimum of 8 years of progressive experience in Quality Control laboratory operations within the life sciences or regulated pharmaceutical/biotech industry.

  • Minimum of 3 years of people leadership experience, with demonstrated success leading, developing, and building capability within QC laboratory teams in a regulated manufacturing environment.

  • Experience managing QC laboratory operations across multiple product lines or manufacturing areas with differing analytical and business requirements.

  • Demonstrated experience partnering with Operations, Manufacturing Sciences, and cross-functional leadership to resolve product and process quality issues related to analytical testing.

  • Experience managing laboratory investigations, deviations, OOS results, and CAPA activities with effective root cause analysis and sustainable corrective actions.

  • Experience applying analytical data, quality metrics, and risk management principles to identify priorities and drive laboratory improvement.

  • Experience supporting regulatory inspections, customer audits, and other audits within a QC laboratory environment.

Knowledge, Skills & Abilities
  • Strong knowledge of analytical testing methods, laboratory operations, and QC practices within a regulated life sciences manufacturing environment, including oversight of laboratories performing molecular biology, biochemical, chromatographic, cell-based, and radiological testing.

  • Working knowledge of applicable safety, regulatory, and compliance requirements for specialized laboratory operations, including BSL-2 environments, radioactive materials and radiation-based assays, and controlled substances, with appropriate understanding of requirements for personnel authorization, safe handling, access and inventory controls, documentation, storage, and disposal.

  • Working knowledge of applicable cGMP, ISO, Quality Management System, and regulatory requirements, including relevant FDA, EMA, and ICH requirements, sufficient to provide effective QC laboratory oversight and leadership.

  • Strong knowledge and practical application of method validation and qualification, laboratory investigations, data integrity requirements, and laboratory information management systems (LIMS).

  • Strong understanding of equipment qualification, calibration, maintenance, and lifecycle requirements for analytical instruments.

  • Demonstrated ability to use laboratory performance data and quality metrics to identify risk, establish priorities, and influence operational improvement.

  • Strong leadership and people-development capabilities, with the ability to build high-performing laboratory teams, develop talent, establish clear accountability, and lead through change.

  • Demonstrated ability to exercise sound scientific judgment and make timely, risk-based decisions in complex situations involving analytical and release testing, manufacturing operations, product quality, and business priorities.

  • Strong cross-functional leadership and influencing skills, with the ability to effectively challenge, align, and partner with Operations, Manufacturing Sciences, Quality Systems & Compliance, Regulatory Affairs, R&D, and other stakeholders.

  • Strong knowledge and application of continuous improvement methodologies, including Practical Process Improvement (PPI), Lean, and/or Six Sigma principles.

  • Excellent written and verbal communication skills, with the ability to clearly communicate quality risks, laboratory priorities, recommendations, and decisions to audiences ranging from technical teams to senior leadership.

  • Demonstrated ability to manage multiple priorities, laboratory capacity, productivity, financials, and resources while appropriately escalating significant risks and maintaining quality standards and compliance.

  • Strong customer focus and commitment to workplace safety, biosafety, radiation safety, data integrity, product quality, and regulatory compliance, with an understanding of how laboratory performance and analytical results impact manufacturing operations and customer outcomes.

Compensation and Benefits
The salary range estimated for this position based in California is $103,100.00-$135,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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