GMP Pharma Production Supervisor

Epicur; Mount Laurel Township (NJ); On-site; USD 34,000 - 49,000; Full time

Benefits offered by this job

Medical, Dental, Vision

Life Insurance

401(k) with employer match

Bonus program

Paid holidays, vacation and personal时间

Excellent working environment

Job summary

Stokes Healthcare in Mount Laurel, NJ seeks a Production Supervisor to lead technicians in a cGMP pharmaceutical manufacturing environment. You will drive quality, compliance and continuous improvement while shaping a high-performance team.

The ideal candidate has 3–5 years in GMP pharma manufacturing, strong leadership, and expertise with GMP documentation, QA collaboration and process optimization. This full-time role offers competitive pay, comprehensive benefits, and a supportive work

Qualifications

• Requires a science-related bachelor’s degree or equivalent work experience.
• Minimum 3–5 years in pharmaceutical manufacturing with GMP exposure.
• Proficiency with ERP/MES/EBR and LIMS systems.
• Experience supervising and developing manufacturing teams.

Responsibilities

• Ensure compliance with cGMP, FDA, ICH and related guidelines.
• Oversee day-to-day manufacturing activities including material requirements and packaging.
• Lead and develop the manufacturing team, set goals, and manage performance.
• Coordinate cross-functional collaboration with Quality Assurance and other departments.
• Support audits and maintain inspection readiness.

Skills

People Development

Communication Skills

Organizational Skills

Problem Solving/Analysis

Results Driven

Technical Capacity

Detail Oriented

Education

Science related bachelor’s degree

Tools

ERP

MES/EBR

LIMS

Job description

Stokes Healthcare in Mount Laurel, NJ seeks a Production Supervisor to lead technicians in a cGMP pharmaceutical manufacturing environment. You will drive quality, compliance and continuous improvement while shaping a high-performance team.

The ideal candidate has 3–5 years in GMP pharma manufacturing, strong leadership, and expertise with GMP documentation, QA collaboration and process optimization. This full-time role offers competitive pay, comprehensive benefits, and a supportive work