Quality Supervisor

Position Summary

The Quality Control Supervisor is responsible for overseeing day-to-day Quality Assurance and Quality Control operations at a new Broomfield, Colorado manufacturing facility producing dietary supplements and cosmetic cleansing bars under FDA cGMP regulations.

This role ensures that all manufacturing, laboratory, and documentation activities comply with applicable regulatory requirements (21 CFR Part 111, cosmetic GMP expectations, and internal quality systems). The Quality Supervisor serves as the on-site quality lead, coordinating cross‑functional activities while maintaining alignment and providing reports to the QA and QC leadership located in the Henderson, Nevada facility.

Key responsibilities include production oversight, laboratory coordination, deviation management, document control support, and team leadership to ensure consistent product quality, compliance, and operational efficiency through effective supervision of Quality Technicians.

• Associate’s degree or higher in a scientific or related field, or equivalent industry experience
• Minimum 5 years of experience in Quality Assurance and/or Quality Control within dietary supplement, pharmaceutical, cosmetic, or food manufacturing environments
• Minimum 2–3 years of supervisory or leadership experience, preferably in a laboratory or manufacturing quality setting
• Working knowledge of FDA cGMP regulations (ANSI 455‑2 and 3, FDA regulations, and 21 CFR Part 111), GLP principles, and Quality systems (deviations, CAPA, change control, document control)
• Experience with laboratory techniques and instrumentation, including Wet chemistry (e.g., titration, extraction, identification), Analytical equipment (HPLC, FTIR, GC, spectroscopy)
• Familiarity with microbiological and/or stability testing (preferred)
• Strong troubleshooting skills for laboratory equipment and processes
• Proficient in Microsoft Office and ability to learn internal Quality Management Systems or Manufacturing Execution System.
• Strong analytical, problem‑solving, and organizational skills
• Detail‑oriented with a strong focus on accuracy and compliance
• Effective written and verbal communication skills, with the ability to interact across all levels of the organization
• Ability to work independently in a new or developing facility environment
• Must be able to work extended hours or weekends as required by business needs

• Oversee daily production activities to ensure compliance with cGMP requirements
• Monitor manufacturing processes with Quality Technicians to ensure in‑process controls and process verifications are completed
• Ensure internal audits and summary reports are generated
• Ensure cleanliness, sanitation, and line clearance requirements are maintained
• Review batch records and production documentation for accuracy, completeness, and compliance
• Ensure real‑time documentation practices are followed by production and quality personnel
• Manage deviations, nonconformances, and investigations, ensuring timely closure and appropriate root cause analysis
• Support CAPA and change control processes, including implementation and follow‑up
• Participate in audits preparation, audits, and support regulatory inspections, ensuring proper responses, and follow‑up activities
• Coordinate with QA/QC leadership at the Henderson Facility and review, revise, and maintain SOPs and quality documentation for the Broomfield Facility
• Audit production records and electronic systems for completeness and accuracy
• Assist in the creation and maintenance of Master Manufacturing Records (MMRs) for facility products
• Oversee label control processes, including issuance, reconciliation, and compliance
• Provide support for document control activities, including SOP management and record retention
• Manage plant‑wide environmental monitoring and pest control
• Supervise laboratory activities, including testing of raw materials, in‑process materials, and finished products
• Oversee laboratory equipment calibration, maintenance, and overall lab operations
• Support laboratory investigations, including OOS/OOT and troubleshooting activities
• Supervise Quality Technicians
• Provide…