Job Description

Quality Supervisor / Manager

Medical Device or Pharmaceutical

As a recognized leader in their industry this multi-national manufacturer continues to grow its brand and expand its market share. This opportunity is available in their Central PA facility. The successful Quality Supervisor/Manager will possess a degree in engineering or similar equivalent education or background. In this role will lead and manage QA and QC functions and staff. You will take the lead in establishing the site Quality Management System and drive compliance and follow-up actions. In addition, you will develop processes and procedures for the manufacturing quality system to ensure product quality. Candidates from a medical device manufacturing setting or cGMP environment are encouraged to apply immediately.

Responsibilities:

  • Define Quality goals
  • Assure compliance with ISO certifications
  • Manage regulatory affairs and supplier quality program.

Requirements:

  • BS in Engineering or related field
  • Minimum 5 years of management experience
  • Background from pharmaceutical production or cGMP

This role is highly visible in this growing manufacturing site. You will interface with the executive team and report to a Corporate Director of Quality. The company offers a competitive salary and comprehensive benefits plan. Individuals interested in advancing their careers and making an impact are encouraged to apply immediately. 

Keywords: cGMP, pharmaceutical, medical device, quality, validation, pharmaceutical production, ISO 9001, ISO 15378, ISO 13485, glass, supplier quality, regulatory affairs, QA, QC, cGMP,

 

Application Instructions

Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!

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