Compounding Manager

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Full Time Broadview, IL, US 1 Attachments

30+ days ago Requisition

The Compounding Manager is responsible for the safe, efficient, and compliant operation of Bradford Labs’ liquid, hot pour, and aerosol compounding functions at the two Illinois manufacturing facilities. This is a working management role - the Compounding Manager is both a hands-on technical resource and a people leader, responsible for directing day-to-day operations, maintaining product quality and GMP compliance, and developing a high-performing team across a growing multi-shift operation.

The Compounding Manager works closely with Operations, Quality, R&D, and Scheduling to ensure production targets are met and standards are upheld.

• Oversee all compounding operations for liquid, hot pour, and aerosol product lines, ensuring output meets scheduled volume, quality, and safety targets.
• Serve as a working manager with direct involvement in formulation execution, equipment setup and troubleshooting, and batch review.
• Monitor and optimize throughput, yields, and cycle times; identify and resolve compounding inefficiencies, capacity constraints, and other execution challenges.
• Ensure accurate and timely completion of batch records, logbooks, and other compounding documentation in compliance with cGMP standards.
• Manage the scheduling and sequencing of compounding runs across shifts in coordination with the Scheduling and Planning function.
• Support the transition from a one-shift to a three-shift operation, including staffing planning, training, and process standardization.

• Ensure all compounding batches meet expected quality standards and pass acceptance testing. Work with the R&D and Quality teams to make appropriate adjustments to batches as needed and in line with acceptable cGMP guidelines.
• Ensure all compounding activities comply with applicable cGMP, FDA, EPA, OSHA, and DOT requirements, including those specific to aerosol manufacturing (propellant handling, pressure vessel regulations).
• Enforce safe handling procedures for flammable, reactive, and pressurized materials; maintain current knowledge of relevant hazard classifications and SDS requirements.
• Ensure team compliance with PPE requirements, lockout/tagout, confined space, and other applicable safety programs.
• Partner with the EHSS function to conduct hazard assessments, support incident investigations, and implement corrective actions.
• Maintain equipment in proper working condition; collaborate with maintenance on preventive maintenance schedules.
• Support internal audits, customer audits, and third-party inspections; assist in developing and responding to audit findings.
• Directly supervise compounding operators and leads across multiple shifts; provide day-to-day direction, performance feedback, and coaching.
• Participate in hiring, onboarding, and training of compounding personnel; build and document SOPs and training materials.
• Conduct performance evaluations; address performance concerns promptly and in partnership with Human Resources.
• Foster a culture of accountability, continuous improvement, and cross-shift consistency and knowledge transfer.
• Develop compounding leads and high-potential operators for increased responsibility as the shift structure expands.

• Collaborate with R&D and Quality on new product scale-up, formula transfers, and process validations.
• Lead or participate in root cause analysis for deviations, OOS results, and customer complaints related to compounding.
• Identify and champion opportunities to improve safety, quality, efficiency, and cost through process and/or equipment changes.
• Maintain current knowledge of industry best practices and regulatory requirements for personal care contract manufacturing.

• 5+ years of experience in a manufacturing compounding, blending, or production role, with at least 2 years in a supervisory or lead capacity. 7+ years preferred
• Demonstrated experience with liquid compounding operations; familiarity with hot pour and/or aerosol manufacturing strongly preferred.
• Working knowledge of cGMP principles and documentation requirements in a personal care, pharmaceutical, or related regulated manufacturing environment.
• Proven ability to lead and develop hourly…