Filtration Sr. Quality Engineer - Columbia, Mo

PPD (Thermo Fisher) UK

Columbia, MO, US
Good manufacturing practices (gmp) compliance
Quality system management including capa and deviation
Root cause analysis and risk assessments
This role supports manufacturing operations within Thermo Fisher Scientific, partnering cross-functionally with Operations, Engineering, Regulatory, and Supply Chain teams to ensure quality excellence and regulatory compliance across the site

Job Summary

  • This role supports manufacturing operations within Thermo Fisher Scientific, partnering cross-functionally with Operations, Engineering, Regulatory, and Supply Chain teams to ensure quality excellence and regulatory compliance across the site.
  • As a Quality Engineer III, you will play a critical role in ensuring our products meet the highest quality and regulatory standards by combining technical expertise with quality leadership.
  • Join our colleagues in bringing our Mission to life every single day—enabling our customers to make the world healthier, cleaner, and safer.

Matching Summary

This role supports manufacturing operations within Thermo Fisher Scientific, partnering cross-functionally with Operations, Engineering, Regulatory, and Supply Chain teams to ensure quality excellence and regulatory compliance across the site.

Skills & Requirements

Must-have

  • Good Manufacturing Practices (GMP) compliance
  • Quality system management including CAPA and deviation
  • Root cause analysis and risk assessments
  • Support for internal and external audits
  • Validation and qualification activities
  • Cross-functional collaboration in manufacturing

Nice-to-have

  • Advanced problem-solving skills
  • Strong project management capabilities
  • Proficiency with Microsoft Office
  • Excellent verbal and written communication
  • Ability to work independently and collaboratively
  • Up to 25% travel flexibility

Key Requirements

  • Advanced Degree with minimum 3 years experience or Bachelor’s Degree with minimum 5 years experience
  • Experience in quality assurance within regulated industries
  • Experience with CAPA, deviations, change control, risk management
  • Experience supporting or leading audits
  • Knowledge of cGMPs, ISO 13485/9001, FDA and EMA regulations
  • Legal authorization to work in the United States without sponsorship
  • Ability to pass background check and drug screening

Work Rights

Must be legally authorized to work in the United States without sponsorship

Tailored Resume

Cover Letter