Trd Sr. Qa Specialist

Novartis

Ivrea, Italy
Onsite
Quality system implementation
Gxp compliance
Audit and inspection support
Support the pilot plant ramp up and operationalization process through the creation compliant manufacturing and QC-related quality system

Job Summary

  • Support the pilot plant ramp up and operationalization process through the creation compliant manufacturing and QC-related quality system.
  • Ensure the compliance of all the business areas with the Novartis Quality Manual and Policies and all relevant GxP, legal and regulatory requirements.
  • Maintain the site compliance through 3rd party management, trainings, change controls, self-inspections, KPIs and KQIs monitoring.

Matching Summary

Support the pilot plant ramp up and operationalization process through the creation compliant manufacturing and QC-related quality system.

Skills & Requirements

Must-have

  • Quality System Implementation
  • GxP Compliance
  • Audit and Inspection Support
  • Change Control Management
  • Supplier Management Activities

Nice-to-have

  • Strong quality mindset
  • Cross-functional collaboration skills
  • Commitment to Diversity and Inclusion

Key Requirements

  • Minimum of 5 years in pharmaceutical industry
  • Previous experience in HAs inspection support
  • Experienced in QMS document management
  • Fluency in English
  • Experience with electronic quality systems

Work Rights

Not specified

Tailored Resume

Cover Letter