R&d Submission & Document Services Lead

Sanofi UK

Hyderabad, India
Not specified; not specified; well-crafted rewards...
5+ years team management in matrix environment
Advanced ectd standards and ctd methodology knowledge
Extensive pharmaceutical regulatory operations experience
This role involves managing a diverse team of regulatory professionals to deliver high-quality, compliant documents for Sanofi's product portfolio

Job Summary

  • This role involves managing a diverse team of regulatory professionals to deliver high-quality, compliant documents for Sanofi's product portfolio.
  • The position requires overseeing document preparation, global submissions, and ensuring adherence to all Sanofi and Health Authority standards.
  • Candidates will drive operational excellence by implementing innovative technologies and continuous process improvements within the Hyderabad Hub.

Matching Summary

This role involves managing a diverse team of regulatory professionals to deliver high-quality, compliant documents for Sanofi's product portfolio.

Salary

Not specified; Not specified; Well-crafted rewards package including healthcare and parental leave

Skills & Requirements

Must-have

  • 5+ years team management in matrix environment
  • Advanced eCTD standards and CTD methodology knowledge
  • Extensive pharmaceutical regulatory operations experience
  • Strong technical aptitude with software troubleshooting

Nice-to-have

  • Continuous process improvement mindset
  • Innovative technological solution implementation
  • Global matrix organization cultural leadership
  • Strategic decision-making input capabilities

Key Requirements

  • Bachelor's degree (Master's preferred) in Regulatory Affairs or Sciences
  • Minimum 5 years experience managing teams in a matrixed environment
  • Proven track record meeting submission timelines and quality standards

Work Rights

Not specified

Tailored Resume

Cover Letter