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Quality Control Laboratory Manager Jobs (NOW HIRING)

Motul

$65K - $70K/yr

General information Reference 2026-1047 Position description Job title QC Laboratory Technician ... manage, and verify laboratory data in LIMS, ensuring accuracy, traceability, and compliance ...

TekWissen LLC

QC Laboratory Associate

Vacaville, CA · On-site

$20 - $25/hr

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Job Title: QC Associate I / QC Laboratory Associate Location: Vacaville, CA - 95688 Duration: 12 ...

City of Santa Cruz

QA/QC Laboratory Chemist

Santa Cruz, CA · On-site

$94.44K - $132.89K/yr

Under direction, the QA/QC Laboratory Chemist coordinates and implements the laboratory's Quality ... Runs the laboratory's information management system (LIMS) by tracking instrument performance ...

Steris Corporation

QC Laboratory Specialist

Mentor, OH · On-site

Position Summary The QC Laboratory Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820 ...

Actalent

QC Laboratory Technician

Saint Paul, MN

$22 - $23/hr

Quality Control Laboratory Technician The Quality Control Laboratory Technician performs analytical ... Manage time and assigned projects efficiently to meet testing priorities and production schedules.

LanceSoft Inc

QC Laboratory Analyst

Winchester, KY

$20.75 - $27.75/hr

Bachelor's degree in Chemistry, Biology, Chemical Engineering or Life Sciences with no work experience OR any other Bachelor's degree with years of experience in a QC laboratory. Minimum skills ...

PL Developments

Quality Control Manager

Miami, FL

The Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory operations to ensure the timely testing, release, and compliance of raw materials, in-process ...

LanceSoft Inc

QC Laboratory Analyst

Winchester, KY

$20.75 - $27.75/hr

Bachelor's degree in Chemistry, Biology, Chemical Engineering or Life Sciences with no work experience OR any other Bachelor's degree with years of experience in a QC laboratory. Minimum skills ...

Marmon

QC Laboratory Technician

Newark, NJ

$20.75 - $26.25/hr

We are located in Newark, NJ and we are seeking a Quality Control Laboratory Technician to work in ... Work cooperatively with team members, associates and manager. * Positively implement company ...

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$30.5K

$81.3K

$129.5K

How much do quality control laboratory manager jobs pay per year?

As of May 31, 2026, the average yearly pay for quality control laboratory manager in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Quality Control Laboratory Manager, and why are they important?

To thrive as a Quality Control Laboratory Manager, you need a strong background in laboratory science, quality assurance, and regulatory compliance, typically supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and certifications such as ASQ Certified Quality Auditor are often required. Excellent leadership, problem-solving, and communication skills help manage teams and ensure smooth operations. These competencies are crucial for maintaining high standards, ensuring product safety, and meeting regulatory requirements in laboratory environments.

What are some common challenges faced by Quality Control Laboratory Managers, and how can they be addressed?

Quality Control Laboratory Managers often face challenges such as maintaining compliance with strict regulatory standards, managing a diverse team, and ensuring timely turnaround of test results. To address these, effective managers implement robust training programs, foster clear communication across teams, and establish standardized operating procedures. Proactive planning and continuous process improvement are key to staying ahead of regulatory updates and ensuring consistent data quality, which ultimately supports both operational efficiency and product safety.

What does a Quality Control Laboratory Manager do?

A Quality Control Laboratory Manager oversees the operations of a laboratory that tests products for quality and compliance with industry standards. They manage laboratory staff, ensure testing procedures are followed accurately, and maintain equipment. The manager is responsible for implementing quality assurance protocols, analyzing test results, and reporting findings to upper management. Their work helps ensure that products meet safety and quality requirements before reaching consumers.

What is the highest paying career in a laboratory?

In a laboratory setting, senior roles such as Laboratory Director or Quality Control Laboratory Manager often have the highest salaries, especially with advanced degrees and extensive experience. These positions typically involve overseeing operations, ensuring compliance, and managing teams, which are compensated accordingly in the industry.

What is the difference between Quality Control Laboratory Manager vs Quality Control Analyst?

AspectQuality Control Laboratory ManagerQuality Control Analyst
CredentialsBachelor's degree in science, often with management certificationsBachelor's degree in science or related field
Work EnvironmentSupervises lab staff, manages operations, oversees testing processesPerforms testing and analysis of samples under supervision
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing industries for lab oversightCommonly employed in similar industries for sample analysis

The main difference is that the Quality Control Laboratory Manager oversees the entire lab operations and staff, ensuring compliance and quality standards, while the Quality Control Analyst focuses on conducting specific tests and analyses. The manager has more responsibilities related to supervision and process management, whereas the analyst is primarily involved in testing tasks.

What cities are hiring for Quality Control Laboratory Manager jobs? Cities with the most Quality Control Laboratory Manager job openings:
What are the most commonly searched types of Quality Control Laboratory jobs? The most popular types of Quality Control Laboratory jobs are:
What states have the most Quality Control Laboratory Manager jobs? States with the most job openings for Quality Control Laboratory Manager jobs include:
Quality Control Laboratory Manager jobs near you
Infographic showing various Quality Control Laboratory Manager job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 95% Full Time, 2% Part Time, 1% Temporary, and 1% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
Manager, Quality - QC Analytical

Manager, Quality - QC Analytical

Glaukos

San Clemente, CA • On-site

Full-time

Posted 14 hours ago

Job description

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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