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Manufacturing Manager (Eng/Spa)

$38 per hour

5TH HQ

Job Description

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.

Vacancy posted a month ago
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