Scientist - Design Control Documentation

Agilent

Not specified; pyy ranges determined by role, leve...
Not specified (assumed to be office-based due to the nature of the role).
Master's degree in relevant field
Experience with design control documentation
Knowledge of iso 13485 and fda 21 cfr part 820
Agilent is seeking a detail-oriented Scientist for Design Control Documentation, focusing on medical device documentation in the diagnostic field, particularly in tissue-based pathology assays like immunohistochemistry. The ideal candidate will have relevant experience and educational background, strong organizational skills, and the ability to collaborate effectively within a team

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 while supporting the New Product Introduction R&D department.
  • The company offers a collaborative work environment with opportunities for career development, pension schemes, and private health care.

Matching Summary

Match Score: 85

Agilent is seeking a detail-oriented Scientist for Design Control Documentation, focusing on medical device documentation in the diagnostic field, particularly in tissue-based pathology assays like immunohistochemistry. The ideal candidate will have relevant experience and educational background, strong organizational skills, and the ability to collaborate effectively within a team.

Salary

Not specified; Pay ranges determined by role, level, and location; Individual pay based on skills and experience

Skills & Requirements

Must-have

  • Master's degree in relevant field
  • Experience with design control documentation
  • Knowledge of ISO 13485 and FDA 21 CFR Part 820

Nice-to-have

  • Familiarity with immunohistochemistry assays
  • Strong attention to detail and organizational skills
  • Excellent written and verbal communication skills

Key Requirements

  • Master's degree or higher in Biochemistry or Biomedical Engineering
  • Proven experience in medical device industry design control
  • Regulatory compliance knowledge (ISO 13485, FDA 21 CFR Part 820)

Work Rights

Not specified

Tailored Resume

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