Supervisor, Quality Systems

West

Jersey Shore, PA, US
On-site
Manage document control activities
Manage capa process
Ensure deviation and nonconformance reports
West is seeking a Supervisor for Quality Systems in Jersey Shore, PA, to manage compliance with quality systems in the pharmaceutical industry. The ideal candidate will have a background in quality management, experience in leading teams, and a strong understanding of cGMP and ISO requirements

Job Summary

  • At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century.
  • Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
  • There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development.

Matching Summary

Match Score: 85

West is seeking a Supervisor for Quality Systems in Jersey Shore, PA, to manage compliance with quality systems in the pharmaceutical industry. The ideal candidate will have a background in quality management, experience in leading teams, and a strong understanding of cGMP and ISO requirements.

Skills & Requirements

Must-have

  • Manage Document Control activities
  • Manage CAPA process
  • Ensure deviation and nonconformance reports
  • Support Technology Transfer process
  • Analyze data and provide reports
  • Ensure proper completion of Change Controls
  • Manage and oversee site quality specialists
  • Review/approve customer specifications
  • Provide for quality planning
  • Submit periodic reports on compliance
  • Monitor and provide guidance to pest control
  • Provide expertise for statistical methods

Nice-to-have

  • Lifelong learning and growth opportunities
  • Inclusive community of professionals
  • Commitment to sustainability efforts
  • Empower physical, mental, emotional, and financial health

Key Requirements

  • Bachelor’s degree in Quality or Engineering
  • At least 3 years of experience
  • One (1) year managing others directly
  • Proficiency in MS Word, Excel and other Microsoft Office Programs
  • Excellent communication skills both oral and written
  • Ability to investigate problems and issues
  • Training in Six Sigma methodology
  • Familiarity with Project Management tools
  • Familiarity with Quality Risk Management
  • Working knowledge of Pharmaceutical Industry requirements
  • Ability to comply with company's safety policy
  • Ability to comply with company's quality policy
  • 5% travel

Work Rights

Not specified

Tailored Resume

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