Specialist - Quality Operations

Novartis UK

United Kingdom
On-site
Cgmp requirements
Novartis quality management system
Analytical method transfers
Novartis UK is seeking a Specialist in Quality Operations to provide quality services in line with cGMP requirements and manage various quality projects. The ideal candidate will have a strong background in Quality Assurance with experience in LabWare LIMS and a commitment to maintaining high standards of pharmaceutical quality

Job Summary

  • Provide quality services in compliance with cGMP requirements and Novartis Quality Management System as defined and agreed between QOP and business partners.
  • Manage Quality aspects & projects within area of responsibility, including coordination and management of analytical method transfers and stability studies.
  • Work on various Labware LIMS workflows including various modules like Lot management, stability management, instrument interfacing, reagent management.

Matching Summary

Match Score: 85

Novartis UK is seeking a Specialist in Quality Operations to provide quality services in line with cGMP requirements and manage various quality projects. The ideal candidate will have a strong background in Quality Assurance with experience in LabWare LIMS and a commitment to maintaining high standards of pharmaceutical quality.

Skills & Requirements

Must-have

  • cGMP requirements
  • Novartis Quality Management System
  • analytical method transfers
  • stability studies
  • LabWare LIMS workflows
  • SAP master data management
  • GxP documents

Nice-to-have

  • global stakeholders
  • dealing with ambiguity
  • digital saviness
  • operational excellence

Key Requirements

  • Min 6 years of experience
  • Pharmacy/ Science/ MBA / M.Tech/MSc /Engineering/ equivalent
  • GxP knowledge
  • Experience with LabWare LIMS application

Work Rights

Not specified

Tailored Resume

Cover Letter