〈研究開発・ﾒﾃﾞｨｶﾙｱﾌｪｱｰｽﾞ統括本部〉薬事本部 Policy And Excellence／担当・担当課長・専門課長／神戸本社・東京支社

Eli Lilly Japan

Kobe, Japan
Not specified; performance-based bonus pyid annual...
**
3+ years pharmaceutical industry experience
Japanese regulatory knowledge
English and japanese communication skills
** Eli Lilly Japan is seeking a qualified candidate for a Regulatory Policy and Excellence role in their Kobe and Tokyo offices. The ideal candidate should possess a background in sciences or medical fields and have significant experience in the pharmaceutical industry, particularly regarding Japanese regulatory knowledge. **

Job Summary

  • The role involves building and maintaining trust relationships with major stakeholders including regulatory authorities and industry associations to monitor regulatory trends.
  • Candidates will lead the creation and maintenance of labeling documents and user manuals while ensuring compliance with the Pharmaceutical Affairs Law.
  • The position offers a flexible work arrangement with a commute limit of 90km or 90 minutes from home to workplace.

Matching Summary

Match Score: 75

** Eli Lilly Japan is seeking a qualified candidate for a Regulatory Policy and Excellence role in their Kobe and Tokyo offices. The ideal candidate should possess a background in sciences or medical fields and have significant experience in the pharmaceutical industry, particularly regarding Japanese regulatory knowledge. **

Salary

Not specified; Performance-based bonus paid annually in March; Housing allowance and commuting expenses provided

Skills & Requirements

Must-have

  • 3+ years pharmaceutical industry experience
  • Japanese regulatory knowledge
  • English and Japanese communication skills
  • Stakeholder relationship management
  • Regulatory document process management

Nice-to-have

  • Strategic thinking capabilities
  • Innovation and continuous improvement culture
  • Global regulatory affairs collaboration
  • Employee engagement and development focus

Key Requirements

  • Bachelor's degree in science or Master's in medical field
  • 3+ years experience in pharma or regulatory authority
  • Knowledge of Japanese drug regulations

Work Rights

Not specified

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