Novo Nordisk Regulatory Professional Job – B Pharma/M Pharma
Dont forget to check out possible interview questions for this job below
Novo Nordisk Regulatory Professional vacancy, Pharmacy job opening 2023, M Pharma job opening 2023, Pharmacy job opening 2023, Novo Nordisk job opening 2023, Pharma job opening 2023, Pharmacy job opening. Intrested and eligible candidates may check out all the details
Job Title: Regulatory Professional II
Department: RA Business Transformation, Global Regulatory Affairs
Job Location: Bengaluru
Eligbility Criteria & Experience
- 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.
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).
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.
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Important Interview Questions and Answers for the above job role:
- What qualifications are required for this position, and what experience do you need to have?
Answer: The ideal candidate for the Regulatory Professional II position should have a Graduate/Postgraduate degree in science/pharmacy or equivalent discipline with 3-6 years of regulatory experience from the pharmaceutical industry. The candidate should also have experience with agile Project Management and the SAFe framework, and experience with Veeva´s Vault RIM suite is an added advantage.
2. What are the key responsibilities of a Regulatory Professional in this role?
Answer: The key responsibilities of a Regulatory Professional II include continuous optimization of the submission process and system, engaging with stakeholders and external vendors, providing technical guidance and regulatory input, ensuring alignment with external regulatory requirements, and playing a key role in stakeholder management.
3. How important is cultural sensitivity in this role, and how would you handle working with colleagues and peers from different countries and cultures?
Answer: High cultural sensitivity is very important for this role, as the candidate will be working with different countries and cultures across multiple time-zones. To handle this, the candidate should be comfortable working with people from different backgrounds, be respectful of different cultures, and be able to communicate effectively with people from different countries.
4. How do you ensure that the adoption of new processes and solutions runs smoothly in the organization?
Answer: To ensure smooth adoption of new processes and solutions, the candidate should engage with stakeholders and external vendors, provide technical guidance and regulatory input, and ensure appropriate use of communication channels to strengthen relationships with stakeholders (both internal and external). Additionally, the candidate should continuously optimize the submission process and system, triggered by evolving business needs and the 3 yearly system releases from Veeva.
5. What does the RA Business Transformation department do, and how does the Regulatory Professional II position fit into this?
Answer: The RA Business Transformation department plays a key role in supporting and enabling the transformation of Regulatory Affairs (RA) across multiple processes and geographies. The department consists of 20 regulatory professionals, Specialists, and Business Analysts located in Denmark and India. The Regulatory Professional II position is responsible for impacting processes and solutions while ensuring business value via smooth adoption in the organization, engaging with stakeholders and external vendors, and ensuring alignment with external regulatory requirements.
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