Lilly – Global Regulatory Affairs – Intern opportunity for all lifesciences candidates at Bangalore

Lilly - Global Regulatory Affairs – Intern opportunity for all lifesciences candidates at Bangalore

Global Regulatory Affairs – Intern opportunity for all Lifesciences candidates at the Bangalore location by Lilly

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Global Regulatory Affairs – Intern

Purpose:

  • The Global Regulatory Affairs Intern is responsible for supporting activities for Lilly drugs, medical devices, and combination device products.
  • The Intern resolves most questions and problems under the supervision of senior colleagues. The Intern develops collegial, mutually productive relationships within the department and cross-functionally and embraces transformation initiatives.

Primary Responsibilities for Global Regulatory Affairs – Intern Lilly:

  • This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.
  • Basic Knowledge of Regulatory Affairs
  • Basic Knowledge of Heath Authorities submission guidelines i.e., European Union, US- FDA and Health Canada, TGA Australia, ICH guidelines, etc.
  • Knowledge of drug discovery & development
  • Awareness of pre-clinical study design, protocol & clinical trials.
  • Basic knowledge of drug packaging, labeling as per guidelines
  • Ability to assess and manage risk in any situation. i.e during project work
  • Strong written, spoken, and presentation communication
  • Attention to detail & Ability to prioritize projects.
  • Effective teamwork skills; able to adapt to diverse interpersonal styles
  • Ability to learn and use new software/technology.
  • Ability to manage multiple tasks simultaneously.
  • Working experience in MS office, Abode Acrobat

Minimum Qualification Requirements for Global Regulatory Affairs – Intern Lilly:

Bachelor’s / master’s degree in a scientific or health sciences discipline (or equivalent experience).

  • Eli Lilly and Company, Lilly USA, LLC, and our wholly owned subsidiaries (collectively “Lilly”) are committed to helping individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request accommodation as part of the application process. Any other correspondence will not receive a response.

ŪLilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability, or any other legally protected status.

Global Regulatory Affairs – Intern Lilly opportunity for all Lifesciences candidates at the Bangalore location Lilly apply here

Lilly - Global Regulatory Affairs – Intern opportunity for all lifesciences candidates at Bangalore
Lilly – Global Regulatory Affairs – Intern opportunity for all lifesciences candidates at Bangalore

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