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Novo Nordisk India Hiring Regulatory Professional II Apply Now

Department:  RA Business Transformation, Global Regulatory Affairs

Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as “Regulatory Professional” with us. “Apply now” – At Novo Nordisk, we assure you will experience the best.

About the department

Global Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk. In this role, you will have the unique opportunity to be part of a strategically crucial business transformation program across multiple processes and geographies and take active part in shaping the way Regulatory Affairs (RA) will work in the future. You will join the RA Business Transformation department that plays a key role to support and enable this transformation. The department consists of 20 regulatory professionals, Specialists and Business Analysts located in Denmark and India. The department is committed towards innovation on the way we work: We embrace a flexible workplace, with a blend of in-office and remote work.

The Position

As Regulatory Professional the responsibilities include continuous optimisation of the submission process and system, triggered by evolving business needs and the 3 yearly system releases from Veeva. The key purpose of the role is to impact processes and solutions while ensuring business value via smooth adoption in the organisation.

Further it requires, engaging with stakeholders and external vendors, providing technical guidance and regulatory input to ensure fit for purpose processes and solutions. This role also requires ensuring alignment with external regulatory requirements. The candidate will play a key role in stakeholder management and will be responsible for ensuring appropriate use of communication channels to strengthen relationships with the stakeholders (both internal and external).

Qualifications

• Graduate/Postgraduate in science/pharmacy or equivalent discipline with 3-6 years of regulatory experience from the pharmaceutical industry.
• Experience with agile Project Management and the SAFe framework is an advantage.
• Experience with Veeva´s Vault RIM suite is an advantage.
• Self-managed, highly proactive, drive and ability to engage with colleagues and peers towards delivering excellent performance and results.
• High cultural sensitivity and comfortable working with different countries and cultures across multiple time-zones.
• Analytical mind-set, flair for IT and excellent written/spoken communication skills.

Working At Novo Nordisk

At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales- we’re all working to move the needle on patient care.

Contact

If you believe you are a match for the above requirements and are willing to take up the role, please apply here with our online application tool. Internal candidates are kindly requested to inform their line Manager before applying. We don’t take applications via direct mail.

Deadline

Apply on or before: 26th April, 2023

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