Regulatory Affairs Specialist Consumer Health

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We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences
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About the Johnson & Johnson Consumer Health
At Johnson & Johnson Consumer, we are dedicated in providing No. 1 consumer brands/products based on consumer and shopper insights. We have a truly unrivalled brand portfolio, with power brands across multiple categories, including Neutrogena, Natusan, Piz Buin, o.b, Imodium, Ipren, Livostin and Nicorette. We're one of the globe's fastest-growing consumer companies, caring for the world, one person at a time, embracing research and science - bringing innovative ideas, products and services to advance the health and well-being of over a billion people every day.


Introduction and Overview
The global and regional regulatory team for Europe, Middle East and Africa (EMEA) is looking for a regulatory specialist. You will join a team with diverse strengths and backgrounds working together in a friendly, encouraging and collaborative atmosphere. The work spans over new product development, life cycle management and monitoring of the external environment which makes this position very attractive for individuals eager to learn and experience different aspects of regulatory.
The role can be based either in Helsingborg (Sweden) or in High Wycombe (UK). The Helsingborg site is a manufacturing and global research & development unit with around 650 employees. R&D focuses on development in three areas: Smoking Cessation, Digestive Health and Cough & Cold. High Wycombe is our centre of excellence for EMEA regulatory, medical and clinical.


Regulatory Affairs Specialist
You will have the responsibility for providing global and regional support to the Digestive Health (DH) and Eye Care (EC) Need States within SelfCare. The position reports to an Associate Director. The individual will predominantly act as the global regulatory lead (GRL) on innovation projects and provide lifecycle management support.


Objectives of the Position
Participate in cross-functional teams as GRL in global projects to deliver new innovations. Work with local and regional Reg colleagues to develop regulatory strategies, coordinate regulatory actions, develop global/regional dossiers and support local review processes
May supervise the Labelling/Safety process
Provide regulatory support to policy, external engagement and issue management
Co-responsible for driving alignment of key processes, simplifications and culture-building activities
Responsible for meeting compliance requirements such as SOP trainings, audits etc.
Support regulatory activities for European procedures and reclassification initiatives
Provide regulatory advice and perform due diligence for product acquisitions and distributor agreements with third parties.
Use effective communication and employ influencing skills to continue to grow key relationships with internal/external contacts.



What you will need to succeed
We are looking for a person with good attention to details and communication skills. It’s crucial that you like working in a multidisciplinary environment and are able to adapt your narrative to your stakeholders. You need to be passionate about learning new things. Successful candidates need to demonstrate they are comfortable in a fast-paced environment and able to prioritize activities wisely.Science degree, preferably MSc or PhD
Minimum 2 years regulatory experience from Pharma, Healthcare, cosmetic or food industry
Detailed understanding and experience of the development and support of OTC medicines is preferred
Excellent communication skills with the ability to lead discussions with various regulatory authorities.
Experience in defining and advancing regulatory strategies and working with multiple internal and external business partners is preferred
Required that candidate has residence today in Sweden or UK.



Application
If you are interested in this position, please apply with a CV and Cover letter. The selection process will start during the standard 30-days posting period, please send in your application as soon as possible. We reserve the rights to close the advert earlier. All applicants can expect feedback on the application.
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