Sr Clinical Quality Specialist

Takeda UK

Mumbai, India
Gcp compliance expertise
Clinical trial regulatory knowledge
Quality management systems experience
The Sr. Quality Specialist is responsible for managing the clinical quality function and ensuring compliance with local clinical trial regulatory requirements

Job Summary

  • The Sr. Quality Specialist is responsible for managing the clinical quality function and ensuring compliance with local clinical trial regulatory requirements.
  • This role involves driving the development and implementation of CQA procedures and local QMS for managing clinical trial quality assurance.
  • The position requires collaboration with local stakeholders to identify quality risk areas and establish appropriate risk mitigations.

Matching Summary

The Sr. Quality Specialist is responsible for managing the clinical quality function and ensuring compliance with local clinical trial regulatory requirements.

Skills & Requirements

Must-have

  • GCP compliance expertise
  • Clinical trial regulatory knowledge
  • Quality management systems experience

Nice-to-have

  • Strong negotiation skills
  • Ability to manage complexity
  • Excellent teamwork and coordination

Key Requirements

  • 7-10 years of experience
  • Life Sciences Graduate/Postgraduate
  • Strong communication skills

Work Rights

Not specified

Tailored Resume

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