Quality Assurance Quality Control Manager

ZOLL

Pawtucket, RI, United States
Base: $100,000.00 to $120,000.00; bonus/equity: el...
On-site
Manage inspection and testing personnel
Investigate quality problems
Create inspection criteria and procedures
ZOLL Medical Corporation is seeking a Quality Assurance Quality Control Manager for its Acute Care Technology division in Pawtucket, RI. The role involves managing quality assurance programs to ensure compliance with established standards and customer specifications while fostering a collaborative team environment

Job Summary

  • This position is responsible for developing, implementing and managing quality assurance and quality control program designed to ensure continuous production of electrodes consistent with established standards, customer specifications and production goals.
  • At ZOLL, we're passionate about improving patient outcomes and helping save lives.
  • The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally.

Matching Summary

Match Score: 85

ZOLL Medical Corporation is seeking a Quality Assurance Quality Control Manager for its Acute Care Technology division in Pawtucket, RI. The role involves managing quality assurance programs to ensure compliance with established standards and customer specifications while fostering a collaborative team environment.

Salary

Base: $100,000.00 to $120,000.00; Bonus/Equity: Eligible for annual bonus; Benefits: Comprehensive benefits plans

Skills & Requirements

Must-have

  • Manage inspection and testing personnel
  • Investigate quality problems
  • Create inspection criteria and procedures
  • Oversee product inspection throughout production
  • Analyze and disseminate quality data
  • Develop quality control training programs
  • Ensure inspection coverage
  • Participate in Material Review Board
  • Act as quality signatory for non-conformances
  • Ensure compliance with GMP, ISO, FDA
  • Promote team environment and collaboration
  • Support internal and external audits
  • Develop quality improvement programs
  • Compile and review monthly quality metrics
  • Lead CAPA investigations
  • Support calibration program maintenance
  • Participate in validation and verification
  • Participate in Change Order review
  • Monitor team workload and performance
  • Assess direct reports' development
  • Conduct performance reviews
  • Participate in hiring and retention
  • Set professional example
  • Execute company strategic business plans
  • Provide leadership and mentorship
  • Mentor cross-functional teams

Nice-to-have

  • Experience with ISO 13485 and FDA QMSR
  • Analytical and diagnostic proficiencies
  • Strong presentation capabilities

Key Requirements

  • Four-year degree in technical or science discipline
  • 4-6 years related experience in regulated environment
  • 1-3 years experience in supervisory/management role

Work Rights

Not specified

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