Senior Professional Quality (m/w/d)

Abbott

Wiesbaden, Germany
Gxp software system validation
Validation documentation review
Software lifecycle monitoring
Ensure GxP conformity of software systems through validation, document review, and lifecycle monitoring

Job Summary

  • Ensure GxP conformity of software systems through validation, document review, and lifecycle monitoring.
  • Collaborate with IT and business departments to support the introduction and modification of regulated applications.
  • Abbott offers career development, an attractive benefits package, and a challenging position in a fast-growing, crisis-proof industry.

Matching Summary

Ensure GxP conformity of software systems through validation, document review, and lifecycle monitoring.

Skills & Requirements

Must-have

  • GxP software system validation
  • validation documentation review
  • software lifecycle monitoring
  • regulatory requirements knowledge
  • CAPA development and implementation

Nice-to-have

  • international company career
  • attractive benefits package
  • dynamic motivated team
  • flat hierarchies open mentality

Key Requirements

  • Minimum 3 years GxP software quality experience
  • Experience in regulated industry
  • Knowledge of FDA 21 CFR Part 11
  • Knowledge of EU Annex 11
  • Experience with GxP environments

Work Rights

Not specified

Tailored Resume

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