Manufacturing Qa Specialist (temporary Position 12 Months)

Agilent Technologies Inc.

Not specified; not specified; core global benefits...
Bachelor's or master's degree in scientific discipline
4+ years experience in medical device or pharma industry
Knowledge of iso 13485, iso 14971, and ivd regulation eu 2017/746
The role involves ensuring compliant and high-quality products for in vitro diagnostic cancer tests through active manufacturing support

Job Summary

  • The role involves ensuring compliant and high-quality products for in vitro diagnostic cancer tests through active manufacturing support.
  • Candidates will serve as a Subject Matter Expert leading improvements within the quality management system and supporting complex investigations.
  • The company offers an inspiring environment with global benefits including an Agilent Result Bonus and Stock Purchase Plan.

Matching Summary

The role involves ensuring compliant and high-quality products for in vitro diagnostic cancer tests through active manufacturing support.

Salary

Not specified; Not specified; Core global benefits including Agilent Result Bonus and Stock Purchase Plan

Skills & Requirements

Must-have

  • Bachelor's or master's degree in scientific discipline
  • 4+ years experience in medical device or pharma industry
  • Knowledge of ISO 13485, ISO 14971, and IVD Regulation EU 2017/746
  • Experience with FDA 21 CFR parts 11 and 820
  • Fluency in Danish and English on business level

Nice-to-have

  • LEAN mindset for process improvement
  • Experience with root cause investigations
  • Ability to work cross-functionally at all levels
  • Proactive team player with detail orientation

Key Requirements

  • Bachelor's or Master's degree required
  • Minimum 4 years industry experience
  • Full fluency in Danish and English required
  • Regulatory knowledge of MDSAP and FDA standards

Work Rights

Not specified

Tailored Resume

Cover Letter