Manager, Quality - QC Analytical

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 ManagementOversees and assigns raw material, in-process, finished product, and stability testing across multiple pharmaceutical products to ensure timely batch release and stability commitmentsManages cGMP stability programs for clinical and commercial products and performs trend analysis to identify risks or emerging issuesOversees the internal reference standard qualification, lifecycle management, and documentation programOversees method validations, verifications, transfers, and feasibility studies to support product development and commercializationOversees audit trail review process and 21 CFR Part 11 complianceEvaluates internal versus external testing strategies and recommends improvements to optimize efficiency, cost, and complianceRecommends laboratory equipment, instrumentation upgrades, and new technologies to support future QC capability needsOversees 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 standardsIdentifies and resolves technical challenges impacting method transfer, assay implementation, and laboratory operationsResponsbile for laboratory budget management such as headcount forecasting, consumables planning, and alignment on capital expenditure planning Documentation & ComplianceReviews and approves analytical data, laboratory documentation, and Certificates of Analysis to ensure accuracy, completeness, and data integrityOversight of audit trail review processAuthors and/or reviews laboratory investigations (OOS, OOT, deviations) and ensures appropriate root cause analysis, impact assessment, and corrective actionsAuthors, reviews, and approves analytical methods, validation protocols, qualification reports, and stability reports to ensure regulatory complianceProvides annual product quality review analytical input Ensures QC documentation, laboratory systems, and practices comply with ICH, USP, Pharm. Eur., JP, and applicable global regulatory guidelinesSupports regulatory submissions by preparing or reviewing technical summariesContributes to SOP development, process improvements, and continuous improvement initiatives within the laboratoryInspection Readiness & Regulatory ActivitiesEnsures 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 appropriatelyAnalyzes and interprets complex analytical data and provides scientifically sound conclusions to support quality and regulatory decisionsParticipates in regulatory inspections and supports responses to regulatory agencies as requiredOwns QC laboratory performance metrics and drives continuous improvement initiatives to improve efficiency and complianceTeam Leadership & Cross-Functional SupportSupervises 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 teamProvides technical leadership, mentorship, development, and performance management for QC chemistsParticipates in cross-functional development and manufacturing meetings as QC representativeCommunicates QC priorities, timelines, and risks to stakeholders and leadershipCollaborates with R&D to assess and implement specialized analytical approaches, when applicableOwnership of QC lab related change control or technical impact assessments and CAPA approval authorityEmploying technical knowledge to assist with Quality risk management (FMEA) and risk management during Quality investigations Digital and Automation StrategyOversee 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#GKOSUSGenerous. 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.Full timePosting Date: 2026-05-01