Nutraceutical Production Supervisor: Lead & Optimize Quality

5th HQ; Town of Florida (NY); On-site; USD 35,000 - 48,000; Full time

Job summary

5th HQ is seeking a Production Supervisor for our Miramar, FL nutraceutical production facility. You will lead daily operations, ensure GMP compliance, and drive improvements while maintaining a safe, productive environment.

The role requires 2+ years in supervision within manufacturing, knowledge of GMP and FDA regulations, and experience with planning, inventory control, and workflow optimization. This is a full-time, on-site position with a Monday–Friday schedule.

Qualifications

• 2+ years in a supervisory role within manufacturing or nutraceutical environment.
• Strong knowledge of GMP, FDA, and industry regulations for nutraceutical production.
• Experience with production planning, inventory control, and workflow optimization.

Responsibilities

• Supervise and coordinate daily production activities to meet targets and quality standards.
• Ensure compliance with GMP, safety regulations, and company policies.
• Monitor production schedules, inventory levels, and workflow efficiency.
• Train, mentor, and supervise production staff to ensure proper execution of duties.
• Identify and implement process improvements to enhance productivity and reduce waste.
• Maintain detailed production reports and track KPIs.
• Coordinate with Quality Control and R&D teams to ensure product specifications.
• Troubleshoot operational issues and provide timely solutions to maintain flow.
• Oversee proper use and maintenance of equipment for safety and efficiency.
• Promote a positive and collaborative work environment.

Skills

2+ years experience

Supervisory experience

Tools

ERP systems

Microsoft Office

Job description

5th HQ is seeking a Production Supervisor for our Miramar, FL nutraceutical production facility. You will lead daily operations, ensure GMP compliance, and drive improvements while maintaining a safe, productive environment.

The role requires 2+ years in supervision within manufacturing, knowledge of GMP and FDA regulations, and experience with planning, inventory control, and workflow optimization. This is a full-time, on-site position with a Monday–Friday schedule.