Scientist - Design Control Documentation

Agilent Technologies Inc.

Not specified; individual pyy determined by locati...
Not specified
Master's degree in biochemistry or biomedical engineering
Experience with design control documentation
Knowledge of iso 13485 and fda 21 cfr part 820
Agilent Technologies is seeking a motivated scientist for the Design Control Documentation role focused on developing medical device documentation for diagnostic use in tissue-based pathology assays. The ideal candidate should have relevant educational qualifications, experience in the medical device industry, and knowledge of regulatory standards

Job Summary

  • The role focuses on developing, reviewing, and maintaining design control documentation for medical devices used in tissue-based pathology assays.
  • Candidates will collaborate with cross-functional teams to ensure accuracy and completeness while supporting the New Product Introduction R&D department.
  • The position offers opportunities for personal career development within an international company dedicated to improving the quality of life through scientific discoveries.

Matching Summary

Match Score: 85

Agilent Technologies is seeking a motivated scientist for the Design Control Documentation role focused on developing medical device documentation for diagnostic use in tissue-based pathology assays. The ideal candidate should have relevant educational qualifications, experience in the medical device industry, and knowledge of regulatory standards.

Salary

Not specified; Individual pay determined by location and experience; Company pension scheme and bonus plan available

Skills & Requirements

Must-have

  • Master's degree in Biochemistry or Biomedical Engineering
  • Experience with design control documentation
  • Knowledge of ISO 13485 and FDA 21 CFR Part 820

Nice-to-have

  • Familiarity with immunohistochemistry and ISH/FISH assays
  • Strong attention to detail and organizational skills
  • Ability to work independently and cross-functionally

Key Requirements

  • Master's degree or higher in relevant field
  • Experience in medical device industry design control
  • Regulatory knowledge of ISO 13485 and FDA 21 CFR Part 820

Work Rights

Not specified

Tailored Resume

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