Regional Medical Safety Officer

Description

Kenvue is currently recruiting for:

Regional Medical Safety Officer, North America

This position reports to Head of Regional Medical and Safety Science, North America and is based at Summit, NJ, USA.

Who we are

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® Brand Adhesive Bandages that you already know and love.

Science is our passion; care is our talent.

Our global team is made up of ~ 22,000 diverse and brilliant people, 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 the life of 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: Head of Regional Medical and Safety Science

Location: Summit, NJ, USA

Travel %: 10

Pay: $238,000 - $322,000

What you will do

The Regional Medical Safety Officer, [North America] is responsible for Provision of medical insights on safety deliverables for the assigned portfolio of products marketed within the region.

This includes:


* Provision of the medical safety inputs to new product development and throughout lifecycle management (PRM review)


* Leading strategy for post-market safety surveillance and risk management activities for products marketed within the region, including ad hoc Safety Management Team (SMT) meetings when needed


* Supporting, in collaboration with Global Risk Assessment and Safety Physicians (GRASPs), global post-market safety surveillance and risk management activities for active ingredients of the medicinal products


* Leading the medical safety evaluations of quality issues with potential impact on safety, in collaboration with other functions within Medical, Clinical and Safety Science (MCSS), Quality and SMT (when needed), and represent at the Quality Review Boards (QRBs)


* Regular or ad-hoc representation at cross-functional forums such as the Qualified Person Responsible for Pharmacovigilance (QPPV) meetings, Technical Review Forums, Medical Safety Council


* Representation at the Complaint Vigilance Review Boards (CVRBs) and provision of medical safety inputs on observed trends and adverse events for products within the region


* Provision of input on licensing and acquisition candidates, as necessary


* Leading safety-related activities and coordinating the response to queries from Regulatory Authorities, commercial partners and internal and external stakeholders on safety concerns and risk management, including development of appropriate documentation in support of new licensing applications/switches.


* Pr...