Specialist Quality Assurance (m/w/d)

Abbott Laboratories GmbH

Neustadt am Rübenberge, Germany
Edms document control
Gmp-relevant workflows
Quality-related documentation
Develop, review, and approve quality-related documents, and support periodic document reviews

Job Summary

  • Develop, review, and approve quality-related documents, and support periodic document reviews.
  • Assist other departments in implementing GMP-relevant workflows and manage GMP-related documentation for plant equipment.
  • Coordinate orders and requests for the QA Systems department and handle authority and customer inquiries.

Matching Summary

Develop, review, and approve quality-related documents, and support periodic document reviews.

Skills & Requirements

Must-have

  • EDMS document control
  • GMP-relevant workflows
  • quality-related documentation
  • equipment documentation management

Nice-to-have

  • analytical thinking
  • initiative and commitment
  • appreciative mentality

Key Requirements

  • Completed training in medical or pharmaceutical field, natural science degree, or comparable qualification
  • Experience in GMP-regulated environment (Quality Assurance)
  • Good MS-Office and SAP knowledge
  • Good English skills

Work Rights

Not specified

Tailored Resume

Cover Letter