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Your Team

As the QC Manager, you will lead and organize the operations of the Microbiology and Chemistry Laboratories. You will work closely with Manufacturing, Supply Chain, Quality, Regulatory, and R&D teams to ensure laboratory testing activities are executed in compliance with FDA regulations, USP standards, company policies, and current Good Manufacturing Practices (cGMPs).

This role is responsible for the development and implementation of laboratory policies, systems, procedures, specifications, and testing programs for Raw Materials, In-Process Materials, Finished Products, Stability Programs, and Method Transfers. You will also oversee laboratory validation activities, quality monitoring programs, and change control processes to support business priorities, quality objectives, and operational excellence.

• Direct and manage all Microbiology and Chemistry Laboratory operations.
• Coordinate laboratory activities with Manufacturing and Supply Chain teams.
• Lead, supervise, train, and develop exempt and non-exempt laboratory personnel.
• Ensure laboratory services are delivered efficiently, cost-effectively, and in compliance with applicable regulations and standards.
• Perform weekly, monthly, and annual reporting as required by site leadership and company procedures.

• Ensure compliance with all applicable FDA, USP, OSHA, EPA, cGMP, corporate, federal, and state requirements.
• Establish, implement, and maintain laboratory standard operating procedures and policies.
• Conduct and approve laboratory investigations, including root cause analysis activities.
• Conduct trend analysis, including Annual Product Review data evaluations.
• Ensure all laboratory changes are appropriately managed through the change control system.
• Maintain accountability for the Product Stability Program.

• Manage the laboratory validation program, including equipment, processes, test methods, software, and related systems.
• Lead and support method transfer activities where applicable.
• Participate in process validation and revalidation programs.
• Oversee testing and analysis of validation samples.
• Support continuous improvement initiatives through laboratory automation and testing method enhancements.

• Ensure laboratory analysts are properly trained and qualified to perform testing activities.
• Verify adherence to Good Laboratory Practices, company standards, and regulatory requirements.
• Routinely audit analyst performance, testing accuracy, and documentation practices to assess training effectiveness and compliance.

• Develop and manage departmental operating and capital budgets.
• Maintain laboratory technologies, software, and equipment in an updated state.
• Prepare and submit capital expenditure requests as needed.
• Ensure all laboratory service contracts are maintained and current.
• Evaluate and manage laboratory maintenance service suppliers.

• Bachelor's degree in Chemistry, Microbiology, or a related scientific discipline.
• Minimum of 8 years of experience in Quality Systems within a regulated environment.
• Minimum of 3 years of management or supervisory experience in a laboratory setting.
• Experience with wet chemistry and/or microbiology laboratory procedures.
• Root Cause Analysis training and practical experience.
• Working knowledge of applied statistics and statistical tools.
• Strong understanding of FDA regulations, USP standards, cGMPs, laboratory operations, and quality systems.
• Experience with laboratory validation programs, method transfers, and stabil
• Proven ability to train, motivate, coach, and develop employees.
• Strong presentation and communication skills.
• Demonstrated success in change management and leading organizational change.
• Demonstrated commitment to integrity, accountability, teamwork, collaboration, and performance excellence.
• Strong facilitation and conflict resolution skills.

• Fully bilingual in English and Spanish.
• Ability to effectively communicate and present information to management, customers, and regulatory auditors.