Head Of Q&v And Digitalization Quality

Roche

Shanghai, China
Not specified (assumed hybrid based on industry standard)
10+ years pharmaceutical industry experience
3+ years people management experience
5+ years gmp facility experience
Roche is seeking a Head of Quality and Digitalization Quality in Shanghai, China, responsible for overseeing validation activities and ensuring compliance with regulatory requirements in the pharmaceutical industry. The role requires significant leadership experience and expertise in quality systems, with a focus on fostering teamwork and driving strategic initiatives

Job Summary

  • The role requires overseeing the technical strategy and direction of validation activities for PT Shanghai across facilities, utilities, and equipment.
  • Candidates must possess expert knowledge of Quality Systems and regulatory guidelines to ensure operations meet Roche standards.
  • The position involves leading a competitive team to deliver performance through strong teamwork and shared responsibilities in a culture of personal expression.

Matching Summary

Match Score: 85

Roche is seeking a Head of Quality and Digitalization Quality in Shanghai, China, responsible for overseeing validation activities and ensuring compliance with regulatory requirements in the pharmaceutical industry. The role requires significant leadership experience and expertise in quality systems, with a focus on fostering teamwork and driving strategic initiatives.

Skills & Requirements

Must-have

  • 10+ years pharmaceutical industry experience
  • 3+ years people management experience
  • 5+ years GMP facility experience
  • Validation Master Plan approval authority
  • Computer System Validation expertise
  • Regulatory compliance interpretation

Nice-to-have

  • Strong cross-functional collaboration skills
  • Ability to drive organizational change
  • Strategic translation of business goals
  • High motivation and team spirit building
  • English and Chinese bilingual communication

Key Requirements

  • Bachelor Degree or above in Pharmacy, Chemistry, or Bioengineering
  • Minimum 10 years work experience in pharmaceutical industry
  • Minimum 3 years people management experience
  • Minimum 5 years experience in commercially licensed GMP facility
  • Bilingual proficiency in English and Chinese

Work Rights

Not specified

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