5TH HQ
Job Description
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 bilingual
Production Coordinator
with 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
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 bilingual
Production Coordinator
with 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