Production Supervisor

2 weeks ago

Middletown, Connecticut, United States Planet Pharma Full time

Position Overview

The Production Supervisor will oversee daily manufacturing operations within a biotech/pharmaceutical facility, ensuring compliance with Good Manufacturing Practices (GMP), safety standards, and company quality objectives. This role requires strong leadership, technical expertise, and the ability to drive operational excellence in a regulated environment.

Key Responsibilities

  • Supervise and coordinate production staff to meet daily, weekly, and monthly output goals.
  • Ensure compliance with FDA, EMA, and GMP regulations in all manufacturing processes.
  • Monitor production schedules, workflows, and resource allocation to optimize efficiency.
  • Train, mentor, and evaluate team members to foster professional growth and maintain high performance.
  • Collaborate with Quality Assurance (QA), Quality Control (QC), Engineering, and Supply Chain teams to resolve issues and improve processes.
  • Maintain accurate production records, batch documentation, and deviation reports.
  • Drive continuous improvement initiatives, including Lean Manufacturing and Six Sigma practices.
  • Enforce safety protocols and maintain a clean, compliant work environment.
  • Support audits and inspections by regulatory agencies and internal stakeholders.
  • Ability to lead cross-functional teams and manage multiple priorities under strict timelines.
  • Proficiency with manufacturing systems (ERP/MES) and Microsoft Office Suite.

Preferred Skills

  • Experience with aseptic processing, biologics, or sterile manufacturing.
  • Familiarity with Lean, Six Sigma, or other continuous improvement methodologies.
  • Knowledge of validation, equipment qualification, and process improvement

Qualifications

Education: BA/BS degree in Life Sciences, Engineering, or related field.

Experience: 3–5 years of supervisory or leadership experience in biotech, pharmaceutical, or related manufacturing environment.

Strong knowledge of GMP, FDA/EMA regulations, and pharmaceutical production processes.

Excellent communication, organizational, and problem-solving skills.

Salary Range: $75,000 to $100,000/yr

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