Safety Operations Specialist I at Novo Nordisk – Bangalore
- About the Role
- Key Responsibilities
- Required Qualifications
- About Global Safety – Global Business Services (GS-GBS)
- How to Apply
- Important Notice
Are you passionate about pharmacovigilance and regulatory compliance? Do you want to be part of a global healthcare leader making a difference in millions of lives? Novo Nordisk invites you to apply for the role of Safety Operations Specialist I in Bangalore, India.
About the Role
As a Safety Operations Specialist I, you will play a vital role in ensuring the safety of medicinal products while adhering to global regulatory standards. You will collaborate across functional areas, implement efficient processes, and contribute to the company’s mission of improving patient lives worldwide.
Key Responsibilities
- Manage adverse event reports and safety information to ensure compliance with global regulations.
- Establish and refine methods to enhance safety deliverables.
- Act as a subject matter expert, supporting quality, processes, and corporate objectives.
- Lead cross-functional projects, defining scopes, deliverables, and stakeholder involvement.
- Oversee deviation and change requests, driving corrective and preventive action plans.
- Support global audits and inspections, presenting safety processes as needed.
- Collaborate with affiliates to implement new processes based on regulatory demands.
Required Qualifications
- Education: Graduation and/or post-graduation in life sciences.
- Experience: Minimum 6 years in pharmacovigilance, with strong knowledge of safety principles and processes.
- Skills:
- Expertise in pharmacovigilance and regulatory guidelines.
- Proficiency in GxP requirements and business process improvements.
- Experience in delivering professional training and support.
- Fluency in English (written and spoken).
About Global Safety – Global Business Services (GS-GBS)
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📱 Get More DetailsSince its establishment in 2010, GS-GBS has been a hub for safety case processing, handling spontaneous, literature, solicited, and clinical trial data. The department also manages safety report submissions, training coordination, ARGUS maintenance, quality assurance, and literature surveillance.
How to Apply
Submit your application online by uploading your CV.
Application Deadline: 10 March 2025
Contact: For further details, visit the Novo Nordisk Careers page.
Important Notice
Beware of fraudulent job offers posing as Novo Nordisk. The company does not charge applicants any fees or request personal financial details during the recruitment process.
To apply for this job please visit careers.novonordisk.com.