Manufacturing Supervisor Position Available In Broward, Florida

Tallo's Job Summary: Join a pharmaceutical company in Miramar, FL as a Manufacturing Supervisor. Earn $19 - $20 an hour with full-time hours. Lead a team, oversee manufacturing operations, ensure compliance with FDA regulations and GMP standards, and drive continuous improvement initiatives. Qualifications include 3 years of supervisory experience and a Bachelor's degree in a related field.

Company:
5th Head Quarters
Salary:
$40560
JobFull-timeOnsite

Job Description

Manufacturing Supervisor 5th

HQ – 5.0

Pembroke Park, FL Job Details Full-time $19 – $20 an hour 16 hours ago Qualifications Bilingual Spanish English GMP Mid-level 3 years High school diploma or GED Supervising experience Bachelor’s degree Manufacturing Leadership Communication skills FDA regulations Full Job Description We are seeking a dedicated and experienced Manufacturing Supervisor to join in a pharmaceutical company in Miramar, FL. The ideal candidate will have a strong background in manufacturing, with a focus on the pharmaceutical industry, and will be responsible for overseeing the daily operations of our manufacturing processes to ensure compliance, efficiency, and safety. Key Responsibilities Lead and manage a team of manufacturing operators and technicians to ensure smooth and efficient production operations during the 2nd shift. Oversee the manufacturing processes, ensuring that production targets are met while maintaining high-quality standards. Ensure that all manufacturing activities comply with FDA regulations, GMP standards, and company policies. Maintain a safe working environment by enforcing safety protocols and conducting regular safety inspections. Train and mentor team members, providing guidance and support to enhance their skills and performance. Conduct regular performance evaluations and provide constructive feedback. Identify and resolve any issues that may arise during the manufacturing process, implementing corrective actions to prevent recurrence. Maintain accurate and up-to-date production records, including batch records, logbooks, and other required documentation. Prepare and present reports on production metrics, quality control, and other relevant data. Drive continuous improvement initiatives to enhance production efficiency, reduce waste, and improve overall product quality. Qualifications Minimum of 3 years of supervisory experience in a pharmaceutical manufacturing environment. Bachelor’s degree in a related field (e.g., Engineering, Chemistry, Pharmaceutical Sciences) is preferred. Strong leadership and communication skills, with the ability to effectively manage and motivate a team. Excellent problem-solving abilities and attention to detail. Bilingual (English/Spanish)

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