Production Supervisor

electroCore IncRockaway, NJ
Onsite

About The Position

This position is responsible for supervising manufacturing personnel to achieve daily production targets. It involves enforcing company WIs (Work Instructions) and SOPs (Standard Operating Procedures) across all manufacturing processes to comply with FDA regulations and ISO 13485 quality standards. The role also includes working with the Quality team to maintain company’s quality standards and track defect rates, and collaborating with the Engineering team to implement lean manufacturing principles and process optimization strategies to increase yield, reduce waste, and enhance efficiency. The primary accountability is to achieve daily production targets while complying with company GMP principles.

Requirements

  • Associate’s degree in engineering, operations management, or a related field is preferred; or a minimum of +5 years of progressive experience in medical Class II device manufacturing.
  • Strong supervisory capabilities.
  • Knowledge of GMP (Good Manufacturing Practices).
  • Understanding of process engineering.

Nice To Haves

  • Certifications such as GMP/ISO standards or Lean Manufacturing are highly preferred.

Responsibilities

  • Supervising the end-to-end manufacturing process of medical products, ensuring they are produced safely, efficiently, and in strict compliance with regulatory standards such as FDA and ISO 13485.
  • Achieving daily production targets.
  • Complying with company GMP principles.
  • Enforcing company WIs (Work Instructions) and SOPs (Standard Operating Procedures) across all manufacturing processes to follow FDA regulations and ISO 13485 quality standards.
  • Working with the Quality team to maintain company’s quality standards and track defect rates.
  • Collaborating with the Engineering team to help implement lean manufacturing principles and process optimization strategies to increase yield, reduce waste, and enhance efficiency.
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