Manufacturing Manager
- Miramar, FL, United States
Location: Miramar, FLCompensation: $30 per hourSchedule:
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Job details
- Pay
- Location: Miramar, FLCompensation: $30 per hourSchedule:
- Education
- Bachelor’s degree
- Experience
- 4–5 years of manufacturing supervisory experience in a cGMP-regulated facility.
- Posting language
- English
- Posted
Original 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, FLCompensation: $30 per hourSchedule:
• 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.
More about this job
Skills
- Leadership
- Regulatory compliance
- Process improvement
- Pharmaceutical processes
- Statistical process control
- Team building
- Communication skills
- Documentation
- Quality control
- Sales
- Quality control systems
- Control production
- Scheduling
- Troubleshoot
- Good manufacturing practices
- Lean manufacturing
- Bilingualism
- Microsoft Office
- ERP