Manager, Quality - QC Analytical

Job-:
Quality Assurance

Location:

San Clemente, CA, United States

Schedule:

Full time Posted:
Job Salary Range:  - 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…