Novo Nordisk Hiring Regulatory Specialist in Bangalore

Novo Nordisk Hiring Regulatory Specialist in Bangalore
  • Full Time
  • Bangalore
  • 25000 INR / Month

Novo Nordisk, a global leader in healthcare, is seeking a Regulatory Specialist to join their team in Bangalore, Karnataka. This role offers a chance to contribute to regulatory compliance, product life cycle management, and strategic regulatory planning. If you have a keen eye for detail, excellent communication skills, and a passion for regulatory affairs, this could be the career move you’ve been waiting for.

Position: Regulatory Specialist

Department: Regulatory Affairs Rare Endocrine Disorders

Location: Bangalore, Karnataka, IN


Responsibilities

As a Regulatory Specialist Global Regulatory Lead (GRL) at Novo Nordisk, your responsibilities will include:

  • Regulatory Submissions: Plan and execute all regulatory submissions worldwide, including strategy development, document creation, file preparation, publishing, distribution, and response to health authorities.
  • Regulatory Interactions: Plan and conduct interactions with health authorities, including meeting preparation, rehearsal, and minute-taking.
  • Core Labeling: Develop and maintain core labeling, ensuring alignment with business opportunities and regulatory requirements throughout the product lifecycle
  • Global Regulatory Lead: Assume leadership for early development projects (G0 to G2), developing regulatory strategies in line with NN Global Project Framework. Serve as the Regulatory Affairs representative in the Project Core Team and Global Project Team, leading and managing all regulatory activities and ensuring alignment with project objectives.
  • Serve as the Regulatory Affairs representative in the Global Project Team (GPT)

Qualifications

To qualify for this role, candidates should have:

  • Master of Science (life sciences) or PhD with 12+ years of relevant regulatory experience.
  • In-depth knowledge of regulatory science in multiple regions.
  • Experience in life cycle management, label development, and health authority interactions.
  • Project management skills and familiarity with the pharmaceutical industry.

About the Department

The Regulatory Affairs department at Novo Nordisk plays a crucial role in ensuring compliance and bringing innovative products to market. They value diversity and expertise, fostering a collaborative environment for professionals from various backgrounds.

Apply online


Working at Novo Nordisk

Novo Nordisk is a global healthcare leader with a commitment to defeating chronic diseases. With a strong legacy in diabetes and a focus on innovation, they impact millions of lives daily. Join a team dedicated to improving patient lives and making a global impact.


Contact and Deadline

If you meet the qualifications and are ready for this role, apply online before 17th May 2024 using Novo Nordisk’s application tool.

To apply for this job please visit careers.novonordisk.com.

Share with your friends and pharma related groups.Join whatsapp - https://bit.ly/whatsapp-pharmastuffTelegram - https://t.me/todaypharmajob

Responses

error

Love this job update? Share it with your friends and help someone find their Job! 🚀💼

RSS200k
Follow by Email20k
Facebook136k
X (Twitter)207k
LinkedIn550k
LinkedIn
Share
Instagram58k
Telegram57k
WhatsApp
Copy link