Regulatory Affairs Expert (m/w/d)

☞ Novo Nordisk

Ver: 113

Dia de atualização: 22-10-2024

Localização: Mainz Rhineland-Palatinate

Categoria: Farmacêutico / Químico / Biotecnologia Farmacêutico / Representantes farmacêuticos

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Conteúdo do emprego

Regulatory Affairs Expert (m/w/d)

Category:Reg Affairs & Safety Pharmacovigilance
Location:Mainz, Rheinland-Pfalz, DE
Life is change - improving lives is our motivation. With over 55.000 employees, we as a global life science company are doing everything we can to conquer chronic diseases. With our innovative medicines, we help millions of people around the world for a better quality of life. To achieve this, we must keep improving as a company and find employees who look forward with us and are highly motivated to follow our path.
Do you have experience in driving strategies and initiatives in Regulatory Affairs and can you demonstrate proven success in influencing health and industry policy? Are you passionate about navigating complex issues and stakeholder landscapes? Are you ready to take on and overcome challenges in your daily work?
If so, then seize the opportunity and apply as our new Regulatory Affairs Expert (m/w/d)

About the department
The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the company. From interacting with healthcare providers, to developing and implementing regulatory strategies, to medical education and collecting data to support efficacy and new product development, CMR is everywhere. What keeps us all marching to the same beat is our patient-centered focus.

The Position
As our Regulatory Affairs Expert, you will be primarily responsible for the regulatory, market-driven management of global product development strategies by ensuring the incorporation of local business needs.
Your tasks will also include:
  • Helping to shape the global strategy for the market approval of development products
  • Regulatory representation in the Therapeutic Area (TA) Squad Teams
  • Regulatory-scientific assessment of global product development plans
  • Initiating and conducting scientific consultations with the responsible authorities

Qualifications
  • Completed scientific studies or approbation as a pharmacist
  • Several years of professional experience in the field of regulatory affairs, strategic mindset and pharma business understanding
  • Knowledge of national and international pharmaceutical and medical device law
  • Profound medical, scientific, and pharmaceutical knowledge
  • In-depth knowledge in market access
  • Enjoy engaging in an agile, crossfunctional and fast-changing environment
  • Fluent in English language

Working at Novo Nordisk
As one of the world’s leading pharmaceutical companies, we at Novo Nordisk have pursued a strong mission since our foundation in 1923: to fight diabetes and other serious chronic diseases. We are proud of our employees. Their enthusiasm and daily commitment are the guarantee of our success. We value their individuality and diversity and want them to develop their talents in a develop their talents in a constructive working atmosphere. We therefore rely on a respectful, integrative, appreciative interaction with each other. Come to Novo Nordisk. Let’s improve the world together!

Contact
Are you interested in this exciting position? Then we look forward to receiving your online application.

Application deadline
Please apply promptly via our online portal, as interviews are conducted on an ongoing basis.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
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Data limite: 06-12-2024

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