Manufacturing Manager

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

Preferred Background :

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 .

Minimum Qualifications :

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.

Key Responsibilities :

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 .

Preferred Skills & Traits :

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.