Manufacturing Supervisor

5th HQ

Pembroke Park (FL)

On-site

USD 23,000 - 32,000

Full time

8 days ago
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Job summary

5th HQ in Miramar, FL is seeking experienced Manufacturing Supervisors to oversee daily operations in a GMP-regulated nutraceutical facility. You will lead production teams, ensure regulatory compliance, and drive operational excellence.

Ideal candidates have leadership experience in pharma/nutrition production, strong communication, and ERP proficiency. This role requires lifting up to 70 lbs, standing for long periods, and offers two shifts: First 6:00 AM–2:30 PM; Second 2:30 PM–11:00 PM, with

Qualifications

  • 1 year of supervisory experience in GMP production.
  • Pharmaceutical or nutraceutical manufacturing preferred.
  • English literacy essential; bilingual English/Spanish a plus.
  • Proficiency with ERP systems beneficial; basic math and computer use.

Responsibilities

  • Supervise daily manufacturing operations (blending, encapsulation, tablet pressing).
  • Ensure GMP, FDA regulations and SOP adherence.
  • Lead and motivate production teams to meet output, safety and quality goals.
  • Perform in-process quality checks and coordinate with QA for inspections and documentation.
  • Monitor production metrics and optimize workflow to reduce downtime.
  • Maintain batch records, production logs, and reports accurately.
  • Identify, report, and help resolve equipment malfunctions and safety issues.
  • Support continuous improvement initiatives for safety, efficiency, and product quality.
  • Enforce safety policies and maintain a clean, compliant production environment.
  • Assist with onboarding, training, and mentoring new employees.

Job description

We are seeking experienced Manufacturing Supervisors to oversee daily operations in a GMP-regulated nutraceutical manufacturing facility. This position plays a critical role in leading production teams, ensuring regulatory compliance, and driving operational excellence. Ideal candidates will have a strong background in nutraceutical or pharmaceutical production, along with proven leadership abilities.

Location: Miramar, FL
Shifts Available:

  • First Shift: 6:00 AM – 2:30 PM

  • Second Shift: 2:30 PM – 11:00 PM
    Pay Rate: $20.00 per hour

Key Responsibilities:
  • Supervise daily operations on the manufacturing floor, including blending, encapsulation, and tablet pressing.

  • Ensure all activities comply with GMP, FDA regulations, and internal SOPs.

  • Lead and motivate production teams to meet or exceed daily output, safety, and quality standards.

  • Conduct in-process quality checks and coordinate with the Quality Assurance team for inspections and documentation.

  • Monitor production metrics and make real-time decisions to optimize workflow and reduce downtime.

  • Maintain accurate and complete documentation including batch records, production logs, and reports.

  • Identify, report, and help resolve equipment malfunctions and safety issues.

  • Support continuous improvement initiatives related to safety, efficiency, and product quality.

  • Enforce safety policies and ensure a clean, organized, and compliant production environment.

  • Assist with onboarding, training, and mentoring new employees.

Minimum Qualifications:
  • High school diploma or equivalent (Associate’s or Bachelor's degree a plus).

  • Minimum 1 year of supervisory experience in a GMP production environment.

  • Previous experience in pharmaceutical or nutraceutical manufacturing preferred.

  • Strong communication, organizational, and leadership skills.

  • Proficiency in basic math and computer use (ERP experience preferred).

  • Ability to read, write, and comprehend instructions in English; bilingual in English/Spanish is a plus.

  • Must be able to regularly lift 30–50 lbs and occasionally up to 70 lbs.

  • Comfortable working in an environment with exposure to vitamins, minerals, herbal ingredients, high noise, and odors.

  • Willingness to stand for extended periods and perform repetitive tasks.

Preferred Skills:
  • Experience with ERP systems and batch documentation.

  • Familiarity with Lean Manufacturing or Six Sigma principles.

  • Bilingual (English/Spanish) communication skills.

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