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Qc Lab Manager Jobs in California (NOW HIRING)

Vie Del

Laboratory Technician

Fresno, CA · On-site

$18.75 - $25/hr

The Lab Technician under close supervision from the Lab Manager and Quality Control Supervisor will perform laboratory tests for such purposes as quality control, process control, and/or product ...

Vie Del

Laboratory Technician

Fresno, CA · On-site

$18 - $20/hr

The Lab Technician under close supervision from the Lab Manager and Quality Control Supervisor will perform laboratory tests for such purposes as quality control, process control, and/or product ...

Rack and Riddle

QC Tech PM

Geyserville, CA · On-site

$21 - $23/hr

This QC & Lab Technician will work with the Production, Winemaking and Lab Teams on all production ... Leads & Management of deviations in quality and will have the authority to stop the line if ...

New

Baxter

Analyst II Quality Control Lab

Hayward, CA

$88K - $121K/yr

... management tools, and self-service applications. * Must be able to read, write, and converse in ... quality, eagerness to learn, and drive for continuous improvement and solutions * Must have the ...

711 Materials, Inc.

Quality Control Technician

Modesto, CA · On-site

$30 - $40/hr

The Quality Control Lab Technician is responsible for inspecting production materials, preparing ... Communicate with upper management and outside companies or agencies to report material testing data

711 Materials, Inc.

Quality Control Technician

Modesto, CA · On-site

$30 - $40/hr

The Quality Control Lab Technician is responsible for inspecting production materials, preparing ... Communicate with upper management and outside companies or agencies to report material testing data

711 Materials, Inc.

Quality Control Technician

Modesto, CA · On-site

$30 - $40/hr

The Quality Control Lab Technician is responsible for inspecting production materials, preparing ... Communicate with upper management and outside companies or agencies to report material testing data

Agilent

Quality Control Laboratory Intern

Carpinteria, CA · On-site

$22 - $25/hr

The Quality Control Laboratory Intern supports day-to-day QC lab operations and assists with ... Support daily lab operations including inventory management, glassware cleaning/sterilization, and ...

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All JobsQc Lab JobsQc Lab Manager JobsQc Lab Manager Jobs in California

Qc Lab Manager information

See California salary details

$30.1K

$80.3K

$127.8K

How much do qc lab manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for qc lab manager in California is $80,259.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,700.00 and $98,700.00 per year, depending on experience, location, and employer.

What is the role of a QC Lab Manager?

A QC Lab Manager oversees quality control testing and analysis in a laboratory setting, ensuring products meet safety and quality standards. They manage laboratory staff, maintain testing protocols, and ensure compliance with industry regulations, often using laboratory information management systems (LIMS).

Is a QC Lab Manager a stressful job?

A QC Lab Manager role can be stressful due to the responsibility for ensuring product quality, strict regulatory compliance, and tight deadlines. Managing laboratory staff, data accuracy, and troubleshooting issues can also contribute to job pressure, especially in industries like pharmaceuticals or manufacturing. However, the level of stress varies based on company size, workload, and individual skills in organization and problem-solving.

What does a QC Lab Manager do?

A QC (Quality Control) Lab Manager is responsible for overseeing the operations of a laboratory that tests products or materials to ensure they meet required quality standards. They supervise laboratory staff, implement quality control procedures, ensure compliance with regulatory requirements, and analyze test results. The QC Lab Manager also manages lab resources, maintains equipment, and works closely with other departments to resolve quality issues and support product development.

What are some common challenges faced by a QC Lab Manager, and how can they be addressed in a fast-paced laboratory environment?

QC Lab Managers often encounter challenges such as maintaining compliance with strict regulatory standards, managing workflow to ensure timely testing, and leading a diverse team with varying levels of experience. These challenges can be addressed by implementing robust quality management systems, fostering ongoing training programs, and utilizing effective communication tools to coordinate tasks. Additionally, strong organizational skills and the ability to prioritize workload are essential for ensuring accuracy and efficiency in a fast-paced lab setting.

What is the difference between Qc Lab Manager vs Qc Technician?

AspectQc Lab ManagerQc Technician
CredentialsBachelor's degree in science, quality assurance certifications often preferredAssociate's or bachelor's degree in science or related field
Work EnvironmentSupervises laboratory staff, manages quality processesPerforms testing and data collection in the lab
Employer & Industry UsageUsed across manufacturing, pharmaceuticals, food industriesCommonly employed in similar industries for testing roles

The Qc Lab Manager oversees laboratory operations, staff, and quality systems, while the Qc Technician focuses on executing tests and recording data. Both roles require scientific knowledge, but the manager has additional responsibilities in supervision and process management.

What are the key skills and qualifications needed to thrive as a QC Lab Manager, and why are they important?

To thrive as a QC Lab Manager, you need a strong background in laboratory science, quality control processes, and leadership, typically backed by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (such as GMP or ISO), and relevant certifications like ASQ CQE are highly valued. Excellent problem-solving, communication, and team management skills set exceptional QC Lab Managers apart. These competencies are critical to ensuring accurate results, regulatory compliance, and efficient lab operations.
What are the most commonly searched types of Qc Lab jobs in California? The most popular types of Qc Lab jobs in California are:
What are popular job titles related to Qc Lab Manager jobs in California? For Qc Lab Manager jobs in California, the most frequently searched job titles are:
What job categories do people searching Qc Lab Manager jobs in California look for? The top searched job categories for Qc Lab Manager jobs in California are:
What cities in California are hiring for Qc Lab Manager jobs? Cities in California with the most Qc Lab Manager job openings:
Qc Lab Manager jobs near you
Infographic showing various Qc Lab Manager job openings in California as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $80,259 per year, or $38.6 per hour.

Manager, Quality - QC Analytical

Glaukos

San Clemente, CA • On-site

Full-time

Re-posted 9 days ago

Job description


How You'll Make an Impact:
The Quality Control Manager in San Clemente, CA oversees all QC laboratory operations and testing activities. This role supervises QC staff, ensures compliant and efficient lab execution, maintains cGMP compliance and data integrity, and provides technical leadership while keeping the laboratory inspection-ready and supporting project teams as needed.
What You'll Do:
General laboratory Management
  • Oversees and assigns raw material, in-process, finished product, and stability testing across multiple pharmaceutical products to ensure timely batch release and stability commitments
  • Manages cGMP stability programs for clinical and commercial products and performs trend analysis to identify risks or emerging issues
  • Oversees the internal reference standard qualification, lifecycle management, and documentation program
  • Oversees method validations, verifications, transfers, and feasibility studies to support product development and commercialization
  • Oversees audit trail review process and 21 CFR Part 11 compliance
  • Evaluates internal versus external testing strategies and recommends improvements to optimize efficiency, cost, and compliance
  • Recommends laboratory equipment, instrumentation upgrades, and new technologies to support future QC capability needs
  • Oversees qualification and calibration of analytical equipment and approves vendor qualification documentation, may include URS development, IQ/OQ/PQ approval authority, equipment lifecycle planning, obsolescence strategy
  • Monitors contract testing laboratories, reviews external analytical data, and ensures CRO/CMO compliance with quality standards
  • Identifies and resolves technical challenges impacting method transfer, assay implementation, and laboratory operations
  • Responsbile for laboratory budget management such as headcount forecasting, consumables planning, and alignment on capital expenditure planning

Documentation & Compliance
  • Reviews and approves analytical data, laboratory documentation, and Certificates of Analysis to ensure accuracy, completeness, and data integrity
  • Oversight of audit trail review process
  • Authors and/or reviews laboratory investigations (OOS, OOT, deviations) and ensures appropriate root cause analysis, impact assessment, and corrective actions
  • Authors, reviews, and approves analytical methods, validation protocols, qualification reports, and stability reports to ensure regulatory compliance
  • Provides annual product quality review analytical input
  • Ensures QC documentation, laboratory systems, and practices comply with ICH, USP, Pharm. Eur., JP, and applicable global regulatory guidelines
  • Supports regulatory submissions by preparing or reviewing technical summaries
  • Contributes to SOP development, process improvements, and continuous improvement initiatives within the laboratory

Inspection Readiness & Regulatory Activities
  • Ensures QC maintains inspection readiness, compliance, and a culture of data integrity
  • Serves as the primary technical lead for QC investigations and escalates significant quality risks appropriately
  • Analyzes and interprets complex analytical data and provides scientifically sound conclusions to support quality and regulatory decisions
  • Participates in regulatory inspections and supports responses to regulatory agencies as required
  • Owns QC laboratory performance metrics and drives continuous improvement initiatives to improve efficiency and compliance

Team Leadership & Cross-Functional Support
  • Supervises QC chemists, sets priorities, and ensures compliant execution of laboratory activities in accordance with cGMP requirements
  • Responsible for QC chemist training matrix updates in coordination with training team
  • Provides technical leadership, mentorship, development, and performance management for QC chemists
  • Participates in cross-functional development and manufacturing meetings as QC representative
  • Communicates QC priorities, timelines, and risks to stakeholders and leadership
  • Collaborates with R&D to assess and implement specialized analytical approaches, when applicable
  • Ownership of QC lab related change control or technical impact assessments and CAPA approval authority
  • Employing technical knowledge to assist with Quality risk management (FMEA) and risk management during Quality investigations

Digital and Automation Strategy
  • Oversee implementation of LIMS / electronic notebooks
  • Improve digital data analytics

How You'll GetThere:
  • 8+ years of experience in analytical chemistry within Pharmaceutical QC environment.
  • Minimum of 1 year of previous management experience in Pharmaceutical QC laboratory, including supervision of QC chemists.
  • Demonstrated leadership skills with the ability to prioritize workload, mentor staff, and ensure inspection readiness and cGMP compliance.
  • Experience managing and overseeing external contract testing laboratories (CROs/CMOs) is preferred.
  • Understanding of analytical platforms including HPLC, FTIR, UV/Vis, and Drug Release.
  • Experience overseeing analytical method validation, verification, method transfer activities, and management of cGMP stability programs.
  • Working knowledge of ICH guidelines, major pharmacopoeias (USP, Ph. Eur., JP), CTD structure, and global regulatory expectations.
  • Strong analytical skills (interpret data, summarize data, present data).
  • Strong written and verbal communication skills. •
  • Motivated and able to work independently, as well as within a team. Exhibits personal integrity, credibility, and responsibility. •
  • Excellent organizational skills and ability to work on multiple projects/tasks. •
  • Meets milestones and schedules.
  • Bachelor's degree in a scientific discipline is required

#GKOSUS
About Us
Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.
Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.
Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.
Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.

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