Bilingual GMP Production Lead (Pharma)

5th HQ

Town of Florida (NY)

On-site

USD 26,000 - 28,000

Full time

4 days ago
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Job summary

5th HQ in Miramar, FL is seeking a dedicated Production Lead to oversee daily manufacturing activities in a pharmaceutical setting. You will lead a team to meet production goals while ensuring quality and regulatory compliance.

The ideal candidate brings at least 2 years in a pharmaceutical or related environment, strong leadership, and hands-on knowledge of GMP standards and FDA regulations. This on-site role offers a weekday schedule and growth opportunities within the industry.

Qualifications

  • Minimum 2 years in a manufacturing or production environment.
  • Pharma experience preferred.
  • Knowledge of GMP and FDA regulations.
  • Strong leadership and communication skills.

Responsibilities

  • Supervise daily production operations to ensure products are manufactured on time and meet quality standards.
  • Train, mentor, and oversee production team members to ensure safety, productivity, and accuracy.
  • Coordinate and schedule production runs to meet deadlines and optimize workflow.
  • Ensure proper documentation of production activities, including batch records, reports, and logs.
  • Communicate production goals, updates, and challenges to management and the production team.
  • Identify and implement process improvements to enhance efficiency and reduce waste.
  • Address and resolve production issues or bottlenecks promptly to minimize downtime.

Skills

Leadership
Communication
Problem solving
Team supervision

Education

High school diploma

Tools

Production software

Job description

5th HQ in Miramar, FL is seeking a dedicated Production Lead to oversee daily manufacturing activities in a pharmaceutical setting. You will lead a team to meet production goals while ensuring quality and regulatory compliance.

The ideal candidate brings at least 2 years in a pharmaceutical or related environment, strong leadership, and hands-on knowledge of GMP standards and FDA regulations. This on-site role offers a weekday schedule and growth opportunities within the industry.

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