Manufacturing Manager EngSpa

5TH HQ; Town of Florida (NY); On-site; USD 44,000 - 61,000; Full time

Job summary

5TH HQ in Miramar, FL is seeking an experienced Manufacturing Manager to lead day-to-day operations in our nutraceutical/pharmaceutical production facility. The ideal candidate has proven leadership in cGMP environments and a strong background in managing production teams, ensuring regulatory compliance, and driving continuous improvement in quality, efficiency, and safety.

Responsibilities include leading the manufacturing department, coordinating with COO and cross-functional teams,

Qualifications

• Bachelor’s degree required in a related field.
• 4–5 years of manufacturing supervisory experience in a cGMP facility.
• Strong leadership and team-building skills.
• Excellent verbal and written communication.
• Ability to analyze production performance and implement improvements.
• Working knowledge of manufacturing documentation, SOPs and QC practices.

Responsibilities

• Lead and manage the manufacturing department to align with company goals.
• Report to the COO and collaborate with QC, Sales, Operations, CEO, CFO.
• Establish production procedures to ensure quality, safety, and efficiency.
• Ensure compliance with cGMP, SOPs, and quality systems.
• Oversee production scheduling, staffing, and shift planning.
• Monitor runs, troubleshoot delays and issues.
• Improve efficiency, machine utilization, and resource allocation.
• Oversee batch record documentation for accuracy and compliance.
• Analyze finished goods for potency, weight, and quality.
• Provide GMP training and safety procedures.
• Promote accident-free work environment through safety protocols.
• Identify cost-saving opportunities; implement lean manufacturing and CI.

Skills

Leadership

Team-building

Communication skills

Production analysis

SOPs & QC

Lean manufacturing

Education

Bachelor’s Degree (B.A. or B.S.)

Tools

Microsoft Office

ERP systems

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:

$38 per hour

Schedule:

Standard Office Hours: 8:30 AM – 5:00 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.