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Country Safety Lead, China Local PV

Type:
Posting Date:
End Date:
Job ID:
2507035759W

Kenvue is currently recruiting for a:

Country Safety Lead, China Local PV

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.  We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to:

国家药物安全负责人

Location:

Asia Pacific, China, Shanghai, Shanghai

Work Location:

Fully Onsite

What you will do

Ensures consistency in global processes by establishing guidelines for clear procedures and overseeing the development of appropriate measures, standard operating procedures and other work practices. Manages participation in quality audits. Coordinates effective responses to internal and external audits of pharmacovigilance activities and the corrective actions arising from these audits. Delivers safety services and assessments for clinical trials and post-marketed products by managing multidisciplinary project teams such as clinical data management, regulatory, and medical. Assesses requirements for quarterly annual reports and coordinates production and distribution. Ensures that reporting timelines are met. Reviews global cases and prepares submissions for local authorities. Controls and assures the quality of the scientific and material content of any documents, files, or other materials sent to customers or regulatory agencies. Reviews target product profiles and drafts summary of product characteristics for new products entering development. Trains all customer facing employees about their pharmacovigilance responsibilities on an annual basis.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.