Associate Principal Scientist

Memorialdrivevetclinic

Hybrid (3 days on-site, 1 day remote)
Regulatory affairs experience
Project and change management
Cross-regional business strategies
Memorialdrivevetclinic is seeking an Associate Principal Scientist to join their global team, focusing on research-intensive biopharmaceutical solutions for human and animal health. The role involves leading cross-regional business strategies and enhancing digital capabilities within the CMC organization while fostering collaboration with internal and external stakeholders

Job Summary

  • We aspire to be the premier research-intensive biopharmaceutical company, at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals.
  • Lead, support or project manage the design and implementation of cross-regional or functional business strategies, process improvement initiatives, and operating model projects in collaboration with our strategic partners.
  • Strengthen Regional CMC’s partnerships with other GRACS and broader enterprise stakeholders across regions, including other GRACS functions, our research & development division functions, and other divisions.

Matching Summary

Match Score: 85

Memorialdrivevetclinic is seeking an Associate Principal Scientist to join their global team, focusing on research-intensive biopharmaceutical solutions for human and animal health. The role involves leading cross-regional business strategies and enhancing digital capabilities within the CMC organization while fostering collaboration with internal and external stakeholders.

Skills & Requirements

Must-have

  • Regulatory Affairs experience
  • project and change management
  • cross-regional business strategies
  • digital transformation capabilities
  • enterprise mindset

Nice-to-have

  • strategic plan facilitation
  • leading-edge science
  • collaboration with strategic partners
  • respectfully challenge thinking

Key Requirements

  • Minimum of 5 years’ experience in regulatory affairs
  • 2+ years’ experience in project and change management
  • Ability to manage complex projects with limited supervision
  • Experience managing cross-functional teams

Work Rights

Not specified

Tailored Resume

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