Cq Staff Specialist Surgery Austria

Johnson & Johnson Johnson & Johnson · Pharma · Wien, Austria

Johnson & Johnson is seeking a CQ Staff Specialist Surgery Austria to establish and lead the overall quality management framework and quality system for the Surgery business in Austria. This role involves ensuring compliance with local regulations, corporate policies, and procedures, managing product quality complaints, adverse events, and field actions, and driving continuous improvement of quality processes. The position requires expertise in QMS, change management, project management, and a detailed understanding of Medical Device regulations.

What you'd actually do

  1. Serve as an SME (Subject Matter Expert) for the assigned Quality System processes e.g. Document & Record Management, Quality Agreements, Change Control, Audit & Inspection, Repack Relabel, Purchasing Controls, CAPA etc…
  2. Provide guidance and support and coaching on assigned processes & systems.
  3. Ensure adequate communication of quality compliance needs and status to all affected sites/organizations.
  4. Drive simplification, standardization and continuous improvement of processes across the EMEA region.
  5. Ensure timely and consistent reporting of metrics and KPIs (Key Performance Indicators) associated with assigned processes.

Skills

Required

  • Bachelor’s degree in engineering, scientific, business or QRC disciplines or equivalent relevant industry experience
  • Compliance experience
  • QMS experience
  • Change management experience
  • Project management experience
  • Strong presentation skills
  • Collaborative approach, team player
  • Managing complexity, working in a matrix organization
  • Detailed understanding of QM Systems and local/regional (EMEA) Medical Device regulations
  • Experience with ISO certification
  • Excellent level of spoken and written German and English

Nice to have

  • Will accept the equivalent relevant industry experience if no degree.

What the JD emphasized

  • Excellent level of spoken and written German and English
  • +5 Years experience in regulated industries; medical device / pharma / consumer.
  • Detailed understanding of QM Systems and local/regional (EMEA) Medical Device regulations.