Manufacturing Manager Position Available In Broward, Florida

Manufacturing Manager 5th

HQ – 5.0

Miramar, FL Job Details Full-time $30 an hour 1 day ago Qualifications Bilingual Spanish

CGMP OSHA

Bachelor of Science ERP systems Process improvement English GMP Mid-level Microsoft Office Six Sigma Supervising experience Bachelor’s degree Continuous improvement Production planning Quality control Manufacturing 4 years Leadership Bachelor of Arts Communication skills Lean manufacturing FDA regulations Full 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 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.