regulatory affairs, senior specialist.

社名
社名非公開

職種
薬事、メディカルライティング

業務内容
Opportunity to work with cutting-edge medical technologies that improve healthcare outcomes worldwide.
emphasizes innovation and invests in research and development, fostering a dynamic and forward-thinking work environment.
Global presence provides employees with opportunities for professional growth and international collaboration.

求められる経験
Education Requirements:
- BA degree in Science is mandatory

Basic Qualifications & Required Experience:
- More than 3 years’ experience regulatory affairs for In-vitro Diagnostics or Medical Devices of Class Ⅲ or Ⅳ.
Business level English.
- Strong interpersonal skills required in the areas of verbal and written communications, focus on regulatory bodies, appropriately responsive to service to internal business needs, coaching, influencing, and team building with growth mindset.
- Strong listening and assessment skills.
- Strong questioning & problem-solving skills.
- Must be self-motivated and self-disciplined and able to prioritize and handle multiple tasks and responsibilities.

保険
健康保険　厚生年金保険　雇用保険,健康保険

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