Production Manager, Compounding Operations
Remedy Logic
Houston, TX · Posted October 14, 2026
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Pay compared with the market
This listing does not state pay. Across 134 open production manager listings that state pay, the middle half runs $90,000 to $123,000 and the median is $105,000.
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About the job
Thirty Madison is now part of Remedy ! You can read more about the acquisition here . We are excited to join forces and continue to revolutionize healthcare accessibility!
As a Production Manager, Compounding Operations, you will oversee daily production activities across sterile and non-sterile compounding operations, ensuring efficient workflows, accurate batch scheduling, and consistent production output while maintaining the highest standards of quality and regulatory compliance.
You will work closely with pharmacy leadership, compounding pharmacists, technicians, and Quality Assurance to optimize production capacity, streamline processes, and support increasing patient demand. This is a hands-on leadership opportunity to help build and scale a growing pharmacy operation, driving operational efficiency, team performance, and continuous improvement across multiple compounding lines.
Comp | Perks | Benefits
Robust and affordable Medical, Dental, and Vision plan options
Vacation time off policy - up to 10 vacation days accrued your first year. Vacation time begins accruing immediately
What you get to do every day
Production Planning & Operations
Oversee daily production activities across sterile and non-sterile compounding lines, ensuring safe, efficient, and timely execution
Develop and manage batch production schedules based on prescription demand, staffing, equipment capacity, and material availability
Coordinate production priorities and workflows to meet operational targets and turnaround times
Monitor production throughput, batch completion, yields, and operational bottlenecks
Optimize equipment utilization, labor allocation, and production resources to maximize efficiency
Partner with pharmacy leadership to forecast production needs and develop capacity plans as volume increases
Ensure production activities follow approved master formulation records, batch instructions, and standard operating procedures
Coordinate equipment readiness, preventative maintenance, and production downtime with appropriate teams
Team Leadership & Development
Provide day-to-day leadership and oversight of compounding production teams, including sterile and non-sterile technicians
Manage staffing schedules, workload distribution, and production priorities to meet operational demands
Establish performance expectations and monitor team productivity, quality, and adherence to procedures
Support onboarding, training, competency development, and ongoing performance management
Partner with pharmacy leadership to identify staffing needs and support team expansion as production volume grows
Foster a culture of accountability, collaboration, patient safety, and continuous improvement
Quality, Compliance & Safety
Partner with Quality Assurance and licensed pharmacy leadership to ensure production operations comply with applicable USP , , and standards, state Board of Pharmacy regulations, and facility SOPs
Ensure production documentation, batch records, equipment logs, and related operational records are accurate and complete
Monitor adherence to established cleaning, sanitation, environmental control, and safety procedures
Identify and escalate production deviations, quality concerns, and out-of-specification results promptly
Support investigations, root cause analysis, and corrective and preventive actions (CAPA) related to production processes
Assist with internal audits, regulatory inspections, and ongoing inspection readiness
Coordinate with Quality Assurance and licensed pharmacists to ensure required quality checks and approvals are completed before product release
Maintain appropriate separation between production responsibilities and independent quality oversight
Process Improvement & Operational Scaling
Identify opportunities to improve production throughput, reduce downtime, minimize waste, and streamline workflows
Develop and implement standardized production processes, scheduling practices, and operational procedures
Establish and track key performance indicators, including batch completion rates, turnaround times, schedule adherence, labor utilization, and production efficiency
Analyze production performance and recommend improvements to increase capacity without compromising quality
Partner with pharmacy leadership, Quality Assurance, and technical teams to resolve operational challenges
Support implementation of new compounding equipment, technologies, and production capabilities
Help develop scalable production systems and processes to support continued growth across sterile and non-sterile operations
What you bring to the role
Bachelor's degree in Operations Management, Pharmaceutical Sciences, Engineering, Chemistry, or a related field, or equivalent relevant experience
5+ years of experience in pharmaceutical manufacturing, compounding pharmacy operations, or a similarly regulated production environment
2+ years of experience managing production teams, supervising manufacturing operations, or leading complex production workflows
Experience with batch scheduling, production planning, resource allocation, and workflow optimization
Working knowledge of pharmaceutical production processes, quality systems, SOPs, and GMP principles
Familiarity with USP , , and requirements and their application to compounding operations
Demonstrated ability to manage production schedules, meet operational targets, and improve efficiency in a regulated environment
Experience partnering with Quality Assurance and technical teams to resolve production issues and maintain compliance
Strong leadership, organizational, analytical, and problem-solving skills
Ability to work independently, prioritize competing demands, and thrive in a fast-paced, growing operation
Bonus points
Direct experience managing sterile and non-sterile compounding operations in a 503A pharmacy or 503B outsourcing facility
Experience in an FDA-registered pharmaceutical manufacturing or outsourcing facility operating under cGMP
Familiarity with specialized pharmaceutical manufacturing equipment, including Korsch tablet presses, hot-melt extrusion (HME), pharmaceutical 3D printing, LMX mixers, capsule fillers, and other compounding technologies
Experience scaling production operations, implementing new equipment, or launching additional production lines
Knowledge of Lean Manufacturing, Six Sigma, or other continuous improvement methodologies
Experience with electronic batch records, pharmacy management systems, manufacturing execution systems (MES), or production reporting tools
Experience supporting regulatory inspections, deviation investigations, and CAPA initiatives
Physical Requirements
Extended periods of standing, walking, and moving throughout pharmacy production areas
Ability to lift up to [35] lbs
Ability to work in controlled production and cleanroom environments requiring appropriate gowning, PPE, and adherence to facility safety protocols
Potential exposure to pharmaceutical ingredients and hazardous drugs with appropriate engineering and PPE controls
Must follow all applicable cleanroom, hygiene, and contamination-control requirements
Must pass fit-testing for respiratory protection where applicable
All Company policies and procedures are subject to change without notice based on business needs. This includes, but is not limited to, the locations where we hire remote, hybrid, or onsite employees.
U.S. Applicants Only
Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Remedy we are dedicated to building a diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions. Contact us at recruiting@thirtymadison.com to request accommodation.
*This employer participates in E-Verify and will provide the federal government with your I-9 Form information to confirm that you are authorized to work in the U.S.*
*Please be aware that there are fraudulent entities who are falsely claiming to be or represent Remedy in order to solicit sensitive personal information or payment. Remedy is not in any way associated with these entities or practices. The safety and integrity of those seeking employment with us is of the utmost importance and we actively work with our legal and security teams to prevent future incidents.
Remedy will never ask for sensitive information or payment when engaging with job seekers. The entities use many methods to perpetuate these scams, including but not limited to: participating in a text-only interview, using Remedy's trademarks on their correspondence, or providing you with a seemingly legitimate offer letter. If you suspect you are a victim of this scamming, we encourage you to cease further contact and report the crime to The Federal Trade Commission .