Associate Principal Scientist

med-in.at

Hybrid (3 days onsite, 1 day remote)
Regulatory affairs experience
Project and change management
Cross-regional business strategies
The Associate Principal Scientist position at med-in.at seeks an experienced professional to lead and support strategic initiatives within the CMC organization, focusing on regulatory affairs and project management. The ideal candidate should possess strong collaboration and communication skills, with a minimum of five years in the regulatory field and experience in project management

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

The Associate Principal Scientist position at med-in.at seeks an experienced professional to lead and support strategic initiatives within the CMC organization, focusing on regulatory affairs and project management. The ideal candidate should possess strong collaboration and communication skills, with a minimum of five years in the regulatory field and experience in project management.

Skills & Requirements

Must-have

  • Regulatory affairs experience
  • Project and change management
  • Cross-regional business strategies
  • Digital capabilities build
  • Enterprise mindset
  • Manage complex projects

Nice-to-have

  • Strategic partners collaboration
  • Innovation and leadership
  • Advance prevention and treatment
  • Respectfully challenge thinking

Key Requirements

  • Minimum of 5 years’ experience in regulatory affairs
  • 2+ years’ experience in project and change management
  • Strong collaboration and communication skills
  • Strong digital skills and familiarity with digital tools and platforms
  • Experience in managing cross-functional teams
  • Experience with CMC regional regulatory strategies is preferred

Work Rights

Not specified

Tailored Resume

Cover Letter