Bilingual Manufacturing Coordinator

5th HQ; Town of Florida (NY); On-site; USD 26,000 - 34,000; Full time

Job summary

5th HQ is seeking a detail-oriented bilingual Production Coordinator for our pharmaceutical/food manufacturing operations in Miramar, FL. You will coordinate daily production activities, ensure FDA and GMP compliance, and support production efficiency and quality.

Ideal candidates have at least 2 years in pharma or food manufacturing, are fluent in English and Spanish, and proficient with Microsoft Office. The role requires strong organizational skills and teamwork in a fast-paced environment.

Qualifications

• Minimum of 2 years of experience in pharmaceutical or food manufacturing.
• Bilingual English/Spanish – required.
• Strong knowledge of FDA, GMP, and safety regulations.
• High School Diploma or GED – required.
• Strong organizational and multitasking skills.
• Proficient in Microsoft Office (Word, Excel, Outlook).
• Excellent communication and interpersonal skills.
• Ability to work in a fast-paced, team-oriented environment.

Responsibilities

• Coordinate and monitor production schedules and workflows.
• Ensure production goals are met while maintaining product quality standards.
• Communicate effectively with supervisors, operators, and quality assurance teams.
• Maintain accurate production records and reports.
• Assist in investigating and resolving production issues or deviations.
• Support audits and ensure ongoing compliance with FDA and GMP standards.

Skills

Bilingual English/Spanish

Strong communication

Microsoft Office

Education

High School Diploma or GED

Tools

Microsoft Office

Job description

Production Coordinator – Pharmaceutical Industry

Location:Miramar, FL

Pay:$22.00/hour

Shift:6:00 AM – 2:00 PM (Monday to Friday)

Job Summary:

We are seeking a detail-oriented and bilingualProduction Coordinatorwith experience in pharmaceutical or food manufacturing to join our team in Miramar, FL. The ideal candidate will coordinate daily production activities, ensure compliance with FDA and GMP regulations, and support overall production efficiency and quality.

Key Responsibilities:

• Coordinate and monitor production schedules and workflows

• Ensure production goals are met while maintaining product quality standards

• Communicate effectively with supervisors, operators, and quality assurance teams

• Maintain accurate production records and reports

• Assist in investigating and resolving production issues or deviations

• Support audits and ensure ongoing compliance with FDA and GMP standards

Requirements:

• Minimum of 2 years of experience in pharmaceutical or food manufacturing

• Bilingual (English/Spanish) – required

• Strong knowledge of FDA, GMP, and safety regulations

• High School Diploma or GED – required

• Strong organizational and multitasking skills

• Proficient in Microsoft Office (Word, Excel, Outlook)

• Excellent communication and interpersonal skills

• Ability to work in a fast-paced, team-oriented environment