Qualified Person

Novartis UK

Ivrea, Italy
Gmp-compliant quality system
Ensure compliance with regulations
Supervise manufacturing processes
Independently supervise manufacturing processes and control testing of the site, operating as Qualified Person according to local law

Job Summary

  • Independently supervise manufacturing processes and control testing of the site, operating as Qualified Person according to local law.
  • Assure compliance to the National Medicines Law and other applicable regulations, maintaining an effective GMP-compliant quality system.
  • Collaborate with Quality Control and Production departments, identify and propose interventions to improve manufacturing processes in terms of quality, productivity, and costs.

Matching Summary

Independently supervise manufacturing processes and control testing of the site, operating as Qualified Person according to local law.

Skills & Requirements

Must-have

  • GMP-compliant quality system
  • ensure compliance with regulations
  • supervise manufacturing processes
  • control testing of the site

Nice-to-have

  • continuous improvement mindset
  • digital savviness
  • dealing with ambiguity
  • leadership
  • problem solving skills

Key Requirements

  • Authorized Qualified Person certificate
  • Degree in Pharmacy, CTF or Chemistry
  • Previous experience in pharmaceutical sterile manufacturing

Work Rights

Not specified

Tailored Resume

Cover Letter