Mumbai

Doctorate in Pharmacy (Pharm.D) or equivalent qualification. Post-doctoral fellowship or experience in clinical pharmacy. Tata Memorial Hospital

Good knowledge in analytical instrumentation commonly used in pharmaceutical testing such as HPLC, UV, Dissolution, FTIR and Karl-Fisher.

Preferred certifications include pharmacovigilance or drug safety training from recognized industry bodies such as DIA or similar professional organizations.

Experience in solid oral dosage and liquid orals formulation & development department for regulated market. 

A minimum of a BA or BS degree in Pharmacy, Nursing, Life Sciences, or related scientific field (or equivalent experience) is required. Johnson & Johnson

Develop and implement effective regulatory strategies and pathways for Sanofi products to enable timely market authorization and product launches

Regulatory Affairs Manager II is a regulatory specialist with project management capabilities responsible for leading the end-to-end planning, coordination, and execution of assigned global deliverables in the maintenance Center of Excellence, as an individual contributor.

Serve as a subject matter expert in regulatory affairs and medical writing for life sciences projects applying deep regulatory domain knowledge to develop compliant documentation and optimize regulatory business processes.

First level manager of a work team that may comprise professionals, technical and/or administrative staff. Typically without budget or hire/fire authority.