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Project Manager Quality Control Jobs in California

Nova Group, Inc.

Quality Control Manager

Napa, CA · On-site

Work closely with the Project Superintendent and Project Manager coordinating quality with production. * Manage and coordinate three phases of control for all features of work. Complete all ...

Nova Group, Inc.

Quality Control Manager

Napa, CA · On-site

Work closely with the Project Superintendent and Project Manager coordinating quality with production. * Manage and coordinate three phases of control for all features of work. Complete all ...

Bachem

Manager / Sr. Manager, Quality Control

Vista, CA · On-site

$133K - $183K/yr

... projects. The Manager / Sr. Manager coordinates both in-house and contract laboratory testing ... Supervise QC Scientists. Provide training, day-to-day scheduling, mentoring, and coaching for QC ...

Bachem

Manager / Sr. Manager, Quality Control

Vista, CA · On-site

$133K - $183K/yr

... projects. The Manager / Sr. Manager coordinates both in-house and contract laboratory testing ... Supervise QC Scientists. Provide training, day-to-day scheduling, mentoring, and coaching for QC ...

Constellation Brands

Quality Control Manager

Napa, CA · On-site

$100K - $153K/yr

Position Summary The Manager, Quality Control provides leadership for production quality ... Strong project management, communication, and leadership skills. * Proficiency with Microsoft ...

Daksta

QA/QC Manager

San Diego, CA · On-site

Job Advertisement: QA/QC Manager, Commercial Overview We are seeking a highly skilled and detail ... Collaborate with project managers, engineers, and contractors to address quality-related issues and ...

Premiere Communications & Consulting

... detail-oriented Quality Control Manager to lead quality assurance, inspection, testing, and ... You'll partner closely with field teams, Project Managers, Superintendents, and leadership to ...

Safety Management

Quality Control Manager

San Diego, CA · On-site

$35 - $45/hr

As a Construction Project Manager, you have the freedom to make decisions, explore new ideas, and ... Manage and maintain the QC software. * Coordinate testing services and additional inspections as ...

JGM Inc.

Quality Control Manager

Los Angeles, CA · On-site

$113K - $125K/yr

Quality Control (QC) Manager Project Duration: October 1, 2026 - August 31, 2028 Position Summary The Quality Control Manager oversees all quality assurance and quality control activities for airport ...

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Project Manager Quality Control information

What is a project manager quality control?

Project Manager Quality Control professionals are responsible for overseeing the quality assurance and quality control aspects of a project. They ensure that all project deliverables meet established standards and regulatory requirements by developing quality management plans, conducting inspections, and coordinating with various teams. Their role is crucial in identifying defects, implementing corrective actions, and maintaining documentation throughout the project lifecycle. By focusing on quality, they help minimize risks, reduce costs, and ensure customer satisfaction.

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

To thrive as a Project Manager Quality Control, you need expertise in quality assurance methodologies, project management principles, and a relevant degree such as engineering or quality management. Familiarity with tools like Six Sigma, ISO standards, project management software (e.g., MS Project), and quality control systems is typically required, along with certifications like PMP or CQE. Strong leadership, problem-solving, and communication skills help ensure effective team coordination and issue resolution. These competencies are crucial for maintaining project quality, meeting regulatory requirements, and delivering successful outcomes on time and within budget.

How does a project manager quality control typically collaborate with cross-functional teams to ensure project deliverables meet quality standards?

A Project Manager in Quality Control works closely with departments such as engineering, production, and compliance to establish quality requirements for each project phase. They facilitate regular meetings to review progress and address quality concerns, coordinate testing and inspection activities, and ensure all stakeholders are aligned on quality objectives. This collaboration helps identify potential issues early and ensures corrective actions are taken promptly, ultimately maintaining the integrity of the project’s deliverables. Building strong communication channels and fostering a culture of accountability are key aspects of this role.

What is the difference between Project Manager Quality Control vs Construction Supervisor?

AspectProject Manager Quality ControlConstruction Supervisor
CertificationsPMI-PMP, Quality certificationsOSHA, OSHA-related certifications
Work EnvironmentOffice, site inspections, quality auditsConstruction sites, overseeing daily operations
Employer & IndustryConstruction firms, project management companiesConstruction companies, general contractors
Primary FocusEnsuring quality standards and complianceManaging daily construction activities and safety

The main difference is that Project Manager Quality Control focuses on maintaining quality standards and compliance throughout a project, often working closely with inspectors and clients. Construction Supervisors oversee daily construction activities, safety, and workforce management on-site. Both roles are essential in construction projects but serve distinct functions.

What cities in California are hiring for Project Manager Quality Control jobs?

Cities in California with the most Project Manager Quality Control job openings:

Project Manager Quality Control jobs near you

Manager, Quality - QC Analytical

San Clemente, CA • On-site

Glaukos
Medical Equipment and Supplies Manufacturing • 51 - 200 employees
Learn more about Glaukosexternal

Full-time

Re-posted 13 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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