Quality Specialist Iii

Thermo Fisher Scientific

Meriden, United States
Base: $83,300.00–$115,000.00; bonus/equity: variab...
On-site
Iso 9001:2015 qms implementation
Internal and external audit programs
Systemic capa implementation
Thermo Fisher Scientific is seeking a Quality Specialist III to oversee quality management systems (QMS) across its manufacturing facilities in Connecticut. The ideal candidate will possess significant experience in quality assurance within regulated industries and will lead audits and corrective action processes while fostering a culture of quality excellence

Job Summary

  • As a Quality Specialist III, you will provide strategic oversight of QMS processes across our two of our CT manufacturing facilities (Meriden and Stafford Springs), lead internal and external audit programs, drive systemic corrective actions (CAPA), and partner cross-functionally with Operations, Engineering, Supply Chain, and Leadership to embed quality into production processes.
  • Lead implementation and maintenance of the QMS aligned with ISO 9001:2015.
  • We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes a choice of national medical and dental plans, and a national vision plan, including health incentive programs.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking a Quality Specialist III to oversee quality management systems (QMS) across its manufacturing facilities in Connecticut. The ideal candidate will possess significant experience in quality assurance within regulated industries and will lead audits and corrective action processes while fostering a culture of quality excellence.

Salary

Base: $83,300.00–$115,000.00; Bonus/Equity: Variable annual bonus based on performance; Benefits: Comprehensive Total Rewards package including medical, dental, vision, PTO, holidays, parental leave, retirement savings, ESPP

Skills & Requirements

Must-have

  • ISO 9001:2015 QMS implementation
  • Internal and external audit programs
  • Systemic CAPA implementation
  • Root cause analysis
  • Quality metrics reporting

Nice-to-have

  • Foster a culture of quality excellence
  • Continuous improvement tools
  • Project management experience

Key Requirements

  • Advanced Degree plus 3 years of experience or Bachelor's Degree plus 5 years of experience
  • Experience in quality assurance/quality control within regulated industries
  • Demonstrated experience leading ISO 9001 QMS initiatives
  • Experience with quality management systems, CAPA processes, deviation management, and change control
  • Proficiency in statistical analysis
  • Strong technical writing skills
  • Experience conducting and hosting internal/external audits

Work Rights

Not specified

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