Operation Investigation Management Specialist

Thermo Fisher Scientific UK

Allschwil, Switzerland
On-site
Gmp standards compliance
Fda regulations knowledge
International quality requirements
Thermo Fisher Scientific is seeking an Operation Investigation Management Specialist in Allschwil, Switzerland, to ensure compliance with GMP standards and support quality assurance in pharmaceutical/biotech manufacturing. The role requires a strong background in quality management systems and involves collaboration with cross-functional teams to maintain high standards and implement improvements

Job Summary

  • Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer.
  • In this role, you'll ensure compliance with GMP standards, FDA regulations, and international quality requirements while supporting manufacturing operations across multiple product lines.
  • Working with cross-functional teams, you'll implement continuous improvement initiatives, conduct investigations, and maintain quality management systems that enable our mission of making the world healthier, cleaner, and safer.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking an Operation Investigation Management Specialist in Allschwil, Switzerland, to ensure compliance with GMP standards and support quality assurance in pharmaceutical/biotech manufacturing. The role requires a strong background in quality management systems and involves collaboration with cross-functional teams to maintain high standards and implement improvements.

Skills & Requirements

Must-have

  • GMP standards compliance
  • FDA regulations knowledge
  • international quality requirements
  • quality management systems
  • deviation investigations
  • CAPA and change control
  • root cause analysis

Nice-to-have

  • continuous improvement initiatives
  • cross-functional team collaboration
  • internal audit experience
  • external regulatory inspection support
  • additional language skills

Key Requirements

  • Bachelor's degree with 2 years of experience
  • Advanced degree with no prior experience
  • Knowledge of cGMP regulations
  • Knowledge of ISO standards (9001/13485)
  • Experience with quality management software systems
  • Fluent English and conversational German (B2)

Work Rights

Not specified

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