Quality Specialist Iii

Thermo Fisher Scientific UK

Meriden, Connecticut, United States
Base: $83,300.00–$115,000.00; bonus/equity: variab...
Hybrid (specific work mode not mentioned, but likely involves some onsite presence)
Iso 9001:2015 qms implementation
Internal and external audit execution
Capa process ownership and verification
Thermo Fisher Scientific is seeking a Quality Specialist III to oversee quality management systems across its Connecticut manufacturing facilities. The role requires experience in ISO 9001 standards, quality assurance, and cross-functional collaboration to ensure compliance and operational excellence

Job Summary

  • This role serves as a subject matter expert in ISO 9001:2015 and manufacturing quality controls to ensure compliance while driving operational excellence.
  • The position involves leading the internal audit program, driving systemic corrective actions, and partnering with Operations, Engineering, and Supply Chain teams.
  • Employees receive a comprehensive Total Rewards package including medical plans, 401(k) retirement savings, and up to 120 hours of paid time off annually.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking a Quality Specialist III to oversee quality management systems across its Connecticut manufacturing facilities. The role requires experience in ISO 9001 standards, quality assurance, and cross-functional collaboration to ensure compliance and operational excellence.

Salary

Base: $83,300.00–$115,000.00; Bonus/Equity: Variable annual bonus eligible; Benefits: Comprehensive medical, dental, vision, 401(k), PTO, and ESPP

Skills & Requirements

Must-have

  • ISO 9001:2015 QMS implementation
  • Internal and external audit execution
  • CAPA process ownership and verification
  • Root cause analysis and investigation
  • Statistical analysis and data trending
  • Regulated industry experience required

Nice-to-have

  • Project management experience preferred
  • Risk assessment methodology knowledge
  • Continuous improvement tools expertise
  • Strong technical writing skills
  • Cross-functional collaboration abilities

Key Requirements

  • Bachelor's Degree plus 5 years experience or Advanced Degree plus 3 years
  • Experience in pharmaceutical, medical device, or biotech industries
  • Proficiency with quality systems software and MS Office Suite

Work Rights

Not specified

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