Description
Kenvue is currently recruiting for:
Senior Associate Medical Affairs CE
This position reports into the Senior Associate Manager Medical Affairs CE and is based in Neuss, Germany.
This is temporary position for 2 years.
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® that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact 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.
What You Will Do
The Senior Associate Medical Affairs CE is responsible for:
- Supporting the team in ensuring the correctness of the information material on OTC medicines for Germany, Austria and Switzerland and offering medical support for the whole CE cluster.
- Being the external and internal contact for the medical-scientific concerns on the OTC drugs.
- Supporting the departments for pharmacovigilance and regulatory affairs in the preparation of relevant medical/clinical texts.
Responsibilities
- Member of the Medical Affairs Department with responsibility for the region Germany, Austria, Switzerland for compliance with the provisions of the AMG, HWG and implementation of the corporate policies; for Austria, in addition to the general requirements of the Unfair Competition Act (UWG), the requirements of the Austrian AMG, V. Section – Advertising restrictions (§§ 50-56a) and the codes of PHARMIG and IGEPHA, must be observed in particular.
- Switzerland: Medical review according to (Arzneimittelwerbeverodnung (AWV), Heilmittelgesetz (HMG) and Pharmakodex).
- Supports MA team in ensuring that the official product information texts as well as the pharmaceutical-scientific information on medicinal products comply with the marketing authorization and other legal requirements in order to guarantee proper care.
- Supports in developing communication for HCP (pharmacists and doctors) and organizes educational events (trainings, symposia).
- Supports Regulatory Affairs Department in the preparation of the necessary scientific information for HCPs as well as the information leaflets for patients in compliance with the legal requirements.
- Participates in the preparation of the registration documents and the product information texts for submission to the national and international registration authorities in cooperation with the specialist departments involved.
- Advises internal and external customers at national and international level on drug-related issues.
- Responds to enquiries from doctors, pharmacists, and patients regarding the correct use of medicines, their pharmaceutical quality, effectiveness, and safety.
- Answers inquiries from practicing pharmacists and hospital pharmacists regarding special pharmaceutical questions such as the interaction between drugs, mechanisms of action as well as the physical and chemical properties (stability, density, pH value, osmolarity...)
- Executes external or internal training courses for pharmacists and doctors or pharmaceutical sales representatives on specific issues in the indication area of Johnson & Johnson OTC drugs.
- Closely cooperates with the drug regulatory affairs, quality department and marketing and sales departments by participating in the planning, coordination and supervision of product management including the development of new marketing strategies.
- Supports the MA team in participation in risk procedures to avert drug risks in cooperation with the German and European regulatory authorities and the supervisory authorities of the federal states.