Novo Nordisk Hiring – Associate Regulatory Professional (2+ Years Exp) | Apply Now!
Novo Nordisk is a global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. With 72,000+ employees and a commitment to impacting 40+ million patient lives daily, we are expanding our regulatory operations to support global healthcare advancements. We are hiring an Associate Regulatory Professional I in Bangalore. If you have experience in Regulatory Affairs, this is an exciting opportunity to grow your career with one of the most innovative pharmaceutical companies in the world!
About Novo Nordisk
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. Our success relies on the joint potential and collaboration of our more than 72,000 employees around the world.
Novo Nordisk Hiring – Associate Regulatory Professional Job Details:
- Job Posting: Associate Regulatory Professional I
- Category: Reg Affairs & Safety Pharmacovigilance
- Location: Bangalore, Karnataka, IN
Novo Nordisk Hiring – Associate Regulatory Professional Position
As an Associate Regulatory Professional I, you will:
- Extend support on the compiling, submission, and approval of Country Specific Submissions files for the responsible countries (NDA, LCM & post approval changes).
- Support affiliates in updating local requirements based on regulatory agencies guidance and input from affiliates/distributors.
- Novo Nordisk Hiring – Associate Regulatory Professional: Manage working relationships with key stakeholders.
- Ensure compliance with regulatory requirements and provide strategic product direction to teams.
- Interact and negotiate with regulatory agency personnel to expedite approval of pending registrations and respond to any questions.
- Serve as a regulatory liaison on the project team throughout the product lifecycle and ensure regulatory impact assessments of production and label changes.
Novo Nordisk Hiring – Associate Regulatory Professional Qualifications
To be successful in this role, you should have:
- Minimum 2+ years of experience in Regulatory Affairs or a related function within the pharmaceutical industry
- Master’s degree in science, Pharmacy, Medicine, or a relevant field.
- Regulatory Affairs Expertise
- Novo Nordisk Hiring – Associate Regulatory Professional. Intermediate knowledge of pharmaceutical regulatory frameworks and industry landscape.
- Familiarity with global and regional regulatory guidelines and compliance requirements.
- Understanding of Regulatory IT systems and tools used in submission and compliance processes.
- Cross-functional business understanding within Regulatory Affairs and related domains.
About the Department
You will be joining the IOSO Regulatory Affairs – OCE team, a dynamic group dedicated to ensuring regulatory compliance for new products and product amendments. Our team is responsible for gaining regulatory approval for clinical trial applications, new drugs, devices, and digital health, as well as expanding the availability of existing products. Located at our headquarters, our department fosters a collaborative and fast-paced atmosphere where you can make a real impact.
Deadline: Apply on or before 14th April 2025.
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