Karnataka

This role serves as a key contributor to regulatory operations by ensuring the accuracy, integrity, and compliance of regulatory information used for global submissions, registrations, product maintenance, and post-market activities.

Basic knowledge on TEVA product portfolio, their therapeutic areas expertise, mechanism of actions and its product/patient safety index.

MSc./ Integrated M.Sc in any branch of Science (e.g. Biology, Chemistry, Physics), MTech., MPharm, M.B.B.S., four-year Bachelors degree or equivalent qualification as per the norms of RCB and from a recognised University or institution. 

M.Pharm (Pharmaceutics or related specialization) with experience in formulation development and evaluations. OR PhD in Pharmaceutical Sciences or related area. Manipal Academy of Higher Education

Collaborate with lab staff to gather study requirements, test article information, and study design details necessary for study initiation, laboratory assignment, and resource planning.

Manage and deliver a wide range of medical writing tasks to a consistently high standard and take the role of Clinical Reporting Project Lead or Medical Writing Lead.

Bachelors or Masters degree in Pharmaceutical Sciences, Life Sciences, Chemistry, Engineering, Sciences, or a related discipline

Demonstrated ability to operationalize local, EU, and global regulatory expectations into fit-for-purpose bioanalytical plans, including inspection readiness, data integrity, and documentation standards.

Retail Business Division of HLL Lifecare Limited has set up AMRIT Pharmacies at NIMHANS Hospital, Bengaluru, Jana Sanjivini Generic Drug Stores (JSGDS) At KC General-Hospital, Sri. Chamarajendra Hospital Premises, Hassan, Victoria Hospital, Bangalore, CV Raman Hospital, Karnataka,