Job opening - Senior Regulatory Affairs Specialist APAC in 東京23区 | Randstad

summary

東京23区, 東京都
¥13,000,000 - ¥16,000,000 per year, 年収1,300 ～ 1,600万円
permanent

job category
biotechnology & pharmaceutical

job details

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 play a key role in shaping regulatory strategies for innovative medical devices across the dynamic APAC region.
Work in a collaborative, global environment with cross-functional teams, gaining exposure to diverse regulatory frameworks and emerging trends. ...

Contribute to impactful projects that improve healthcare outcomes, while advancing your career in regulatory affairs within the medical device industry.

求められる経験
Experience & Skill:
● At least 5 years of experience in regulatory affairs within the medical device industry.
● Strong knowledge of international medical device regulations.
● General understanding of product development and design control processes.
● Skilled at managing multiple projects of varying complexity while meeting deadlines.
● Effective in research, analysis, and problem-solving.
Excellent written, oral, and technical writing skills with the ability to simplify complex information.
● Quick learner, self-motivated, and able to work independently with minimal supervision.
● Capable of building a wide range of business relationships.
Team player with strong interpersonal skills.

保険
健康保険　厚生年金保険　雇用保険,健康保険,厚生年金保険,介護保険

休日休暇
土曜日　日曜日　祝日

給与
年収1,300 ～ 1,600万円

賞与
Variable
雇用期間
期間の定めなし

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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 play a key role in shaping regulatory strategies for innovative medical devices across the dynamic APAC region.
Work in a collaborative, global environment with cross-functional teams, gaining exposure to diverse regulatory frameworks and emerging trends.
Contribute to impactful projects that improve healthcare outcomes, while advancing your career in regulatory affairs within the medical device industry.

求められる経験
Experience & Skill:
● At least 5 years of experience in regulatory affairs within the medical device industry.
● Strong knowledge of international medical device regulations.
● General understanding of product development and design control processes.
● Skilled at managing multiple projects of varying complexity while meeting deadlines.
● Effective in research, analysis, and problem-solving.
Excellent written, oral, and technical writing skills with the ability to simplify complex information.
● Quick learner, self-motivated, and able to work independently with minimal supervision.
● Capable of building a wide range of business relationships. ...

show more

experience
Experience & Skill: ● At least 5 years of experience in regulatory affairs within the medical device

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