Job Posting Title Quality Engineering, Qa Expert, Project Delivery (cq & Csv)

Lonza Group

Hyderabad, India
Cgmp pharmaceutical manufacturing compliance
Equipment and computerized system qualification
Commissioning, qualification, and validation protocols
This role ensures qualification and validation compliance for equipment and computerized systems used in cGMP pharmaceutical manufacturing

Job Summary

  • This role ensures qualification and validation compliance for equipment and computerized systems used in cGMP pharmaceutical manufacturing.
  • The QA Expert acts as the voice of Global QA in cross-functional teams to ensure alignment with Lonza's global engineering standards.
  • Candidates must uphold data integrity principles while supporting inspection readiness and audit activities for growth projects.

Matching Summary

This role ensures qualification and validation compliance for equipment and computerized systems used in cGMP pharmaceutical manufacturing.

Skills & Requirements

Must-have

  • cGMP pharmaceutical manufacturing compliance
  • equipment and computerized system qualification
  • commissioning, qualification, and validation protocols
  • FDA and Swissmedic regulatory requirements
  • data integrity principles evaluation

Nice-to-have

  • cross-functional stakeholder management skills
  • proactive risk management approach
  • continuous improvement translation of trends
  • harmonization of global engineering standards

Key Requirements

  • Bachelor's or Master's degree in Engineering or Biological Sciences
  • Strong background in qualification, validation, and compliance within regulated pharmaceutical environment
  • Experience with GMP regulations and global quality standards
  • Business fluent in English

Work Rights

Not specified

Tailored Resume

Cover Letter