Trd Qa Specialist

Novartis

Ivrea, Italy
Onsite
Sterile pharmaceutical manufacturing
Quality systems and data integrity
Aseptic processing knowledge
Support the pilot plant ramp-up and operationalization by contributing to the development, implementation, and maintenance of a compliant manufacturing and QC quality system

Job Summary

  • Support the pilot plant ramp-up and operationalization by contributing to the development, implementation, and maintenance of a compliant manufacturing and QC quality system.
  • In routine operations, coordinate and provide leadership to the QA shopfloor team, ensuring continuous QA presence during manufacturing and QC activities.
  • Manage and oversee GxP Quality System processes, including Change Control, Deviation Management and CAPA, ensuring full compliance with GxP requirements and the Novartis Quality Manual.

Matching Summary

Support the pilot plant ramp-up and operationalization by contributing to the development, implementation, and maintenance of a compliant manufacturing and QC quality system.

Skills & Requirements

Must-have

  • Sterile pharmaceutical manufacturing
  • Quality Systems and Data Integrity
  • Aseptic processing knowledge
  • GxP Quality System processes
  • Manufacturing and QC oversight

Nice-to-have

  • Digital saviness
  • Business Partnering
  • Dealing With Ambiguity
  • Continuous improvement mindset
  • Cross-functional attitude

Key Requirements

  • Minimum 3 years shopfloor experience
  • Sterile pharmaceutical manufacturing experience
  • Quality Systems knowledge
  • Data Integrity principles
  • Aseptic processing experience
  • Electronic quality systems experience

Work Rights

Not specified

Tailored Resume

Cover Letter