Executive - Regulatory Affairs - Mumbai, India - Novartis
Description
1,800+ associates. 85+ countries. 1 goal.At Novartis, we are dedicated to discovering and developing new treatments for diseases including cancer, heart disease, and neurological conditions—and delivering them at a scale to reach as many patients as possible.
Novartis has a unique and promising portfolio with approximately 70 projects as potential NMEs in development, 52 projects in Phase 3 or already undergoing registration, and 100 Phase 1/2 projects.
And you could be at the center of it all in Regulatory Affairs (RA), where your voice, experience, and quality mindset can truly make a difference in drug development at Novartis.
Read on to learn about the role available in RA. We hope you will consider joining our global RA family.Your responsibilities include, but are not limited to:
- Manages medium to small level global regulatory submission projects.
- Provide submission and contribute to the technical related regulatory strategy, intelligence and knowledge required to develop, register, and maintain global products.
- Contribute to strategic and technical input /support to drive implementation of global
products.
- Write, edit and /or manage the production of high quality clinical documentation (e.g.
Developing professional expertise, applies company policies & procedures to resolve a
variety of issues. Frequent internal company and external contacts. Represents organization on specific projects
- Works on problems of moderate scope where analysis of situations or data requires a review
- Refers to established policies & procedures for guidance.
- Contributes to some cost center goals & objectives. Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt. Distribution of marketing samples (where applicable)
Commitment to Diversity & Inclusion:
- We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._
Minimum requirements
- 2+ years of relevant experience in Data Science
- Collaborating across boundaries
- Cross Cultural Experience
- Functional Breadth
- Operations Management and Execution
- Process management, Project Management, Technical knowledge
- Working experience within the pharmaceutical industry
WHY NOVARTIS
769 million lives were touched by Novartis medicines in 2020, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility.
And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges.
Because the greatest risk in life, is the risk of never trying Imagine what you could do here at NovartisCommitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve.
Division
Global Drug Development
Business Unit
REG AFFAIRS GDD
Country
India
Work Location
Mumbai
Company/Legal Entity
Nov Hltcr Shared Services Ind
Functional Area
Research & Development
Job Type
Full Time
Employment Type
Regular
Shift Work
No
Early Talent
No
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