Product License Maintenance Manager

pfizer.dk

Regulatory submissions preparation
Document management standards
Enterprise regulatory systems
Your role will be instrumental in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards

Job Summary

  • Your role will be instrumental in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards.
  • Coordinate enterprise-wide regulatory management systems, train team members, and develop and implement strategic plans.
  • Collaborate with team managers to forecast and manage project-specific resources, utilizing flexible resourcing and global load sharing as standard practice.

Matching Summary

Your role will be instrumental in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards.

Skills & Requirements

Must-have

  • regulatory submissions preparation
  • document management standards
  • enterprise regulatory systems
  • interpretation of regulatory guidelines
  • global regulatory submissions

Nice-to-have

  • AI tools for productivity
  • responsible AI practices
  • pharmaceutical organizational structures
  • project management experience

Key Requirements

  • BA/BS with 2+ years experience
  • MBA/MS with any years experience
  • Deep understanding of drug development
  • Familiarity with submission systems
  • Proficiency in English

Work Rights

Not specified

Tailored Resume

Cover Letter