Qa Specialist

Johnson & Johnson MedTech

Xian, Shaanxi, China
Gmp compliance and supervision
Production and packaging batch record review
Capa management and closure
Johnson & Johnson MedTech fosters an inclusive work environment valuing diversity and individual merit

Job Summary

  • Johnson & Johnson MedTech fosters an inclusive work environment valuing diversity and individual merit.
  • The QA Specialist will manage GMP compliance, conduct audits, oversee quality investigations, and ensure safety management of special drugs.
  • The role requires strong communication and cross-department collaboration to maintain high standards in pharmaceutical production quality.

Matching Summary

Johnson & Johnson MedTech fosters an inclusive work environment valuing diversity and individual merit.

Skills & Requirements

Must-have

  • GMP compliance and supervision
  • Production and packaging batch record review
  • CAPA management and closure
  • Quality system management and investigation
  • SAP system maintenance
  • Safety management of special drugs
  • Training and qualification of QA personnel

Nice-to-have

  • Project management experience
  • Collaboration and team spirit
  • Fluent written and spoken English
  • Ability to work under tight deadlines
  • Innovative and change-driven mindset
  • Strong communication and negotiation skills
  • Proficient in Windows and office software

Key Requirements

  • 5 years pharmaceutical industry experience
  • 3 years multinational company experience
  • Bachelor degree or above in pharmaceutical, chemical, biochemical, or pharmaceutical engineering
  • Fluent in written and spoken English
  • GMP knowledge and experience
  • Experience with quality control and document management
  • Ability to conduct internal audits

Work Rights

Not specified

Tailored Resume

Cover Letter