Manufacturing Manager

Job Description

Job Description

We are seeking an experienced Manufacturing Manager to lead and oversee day-to-day operations within our nutraceutical/pharmaceutical production facility. The ideal candidate will bring proven leadership in cGMP-compliant environments and possess a strong background in managing production teams, ensuring regulatory compliance, and driving continuous improvement in quality, efficiency, and safety.

Location: Miramar, FL
Compensation: $30 per hour
Schedule:

• Standard Office Hours: 8:30 AM – 5:00 PM

• Flex Shift (as needed): 10:00 AM – 7:00 PM

• Prior experience in nutraceutical or pharmaceutical manufacturing is highly preferred.

• Strong understanding of OSHA , FDA , and cGMP regulations.

• Familiarity with world-class manufacturing methods and statistical process control .

• Bachelor’s Degree (B.A. or B.S.) required.

• 4–5 years of manufacturing supervisory experience in a cGMP-regulated facility.

• Strong leadership and team-building skills.

• Excellent verbal and written communication skills.

• Proven ability to analyze production performance and implement improvements.

• Working knowledge of manufacturing documentation , SOPs, and quality control practices.

• Lead and manage the manufacturing department , ensuring smooth daily operations and alignment with company goals.

• Report directly to the COO while collaborating cross-functionally with QC, Sales, Operations, CEO, and CFO .

• Establish and enforce production procedures to maintain high-quality standards, safety, and operational efficiency.

• Ensure compliance with cGMP , SOPs, and company quality systems.

• Oversee production scheduling, staffing, and shift planning—including managing overtime and additional shifts as necessary.

• Monitor production runs to ensure they stay on schedule and troubleshoot any delays or issues.

• Continuously evaluate and improve efficiency , machine utilization , and resource allocation .

• Oversee batch record documentation, ensuring accuracy , completeness , and compliance with regulations.

• Analyze finished goods (capsules and tablets) to ensure they meet specifications for potency, weight, and quality.

• Provide regular training to team members on GMP practices , SOP compliance , and safety procedures .

• Promote a clean, organized, and accident-free work environment by enforcing all safety protocols.

• Identify areas for cost savings and implement strategies for lean manufacturing and continuous improvement .

• Bilingual (English/Spanish) is a plus.

• Proficient in Microsoft Office and experience with ERP systems .

• Knowledge of Lean Manufacturing , Six Sigma , or similar process improvement methodologies is beneficial.