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5th HQ

Manufacturing Manager

5th HQ, Hollywood, Florida, United States, 33024

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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.