Kenvue 目前正在招聘 a：
我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
法规事务副总监位置：
Asia Pacific, China, Shanghai, Shanghai工作地點：
完全現場你會做什麼
Position Summary
· Develop problem-solving strategies which drive efficiency within the project teams, ensure product compliance and deliver high-quality submissions per project timelines for both NPD and LCM projects. (e.g. ANDA/NDA, variations, renewals etc.)
· Build strategic regulatory insights in Big-health industry, provide innovative regulatory strategies/direction to the business for relevant selfcare products and seek potential regulatory innovation opportunities to accelerate & optimize the registration pathway.
· Provide thorough assessment to establish the feasible registration pathway of pipeline/projects /claim innovation with excellent execution to ensure fast introduction and enrich selfcare portfolio ((OTC, Medical Device, Health Food, etc.)
· End to end regulatory lead for submission strategy & dossier process also post submission communications ensure success registration & product speed to market.
· Establish and maintain good connections with regulatory authorities (Provincial FDA, NMPA, CDE, CFDI, etc.) to ensure effective product registrations. Support on Self care external engagement to positively shape the favorable regulatory environment.
· Proactively partner with internal business stakeholders (local, regional, global) to develop of innovative regulatory strategies & excellent execution to ensure that regulatory requirements are incorporated upfront and project risks are understood and mitigations in place.
Required Qualifications
Required Minimum Education: Minimum Bachelor Degree in Pharmacy, Biology, Chemistry or related Life Sciences.
Required Years of Related Experience: Preferred minimum 3 years’ experience in Regulatory Affairs.
Required Knowledge, Skills and Abilities:Experience and knowledge of regulatory requirements relevant for the categories relevant for the company.
Skillful written and fluent spoken in English and Mandarin.
Competencies: Agile and efficient thinking; Able to think business strategically; excellent execution； Risk analysis/management;.
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