Gujarat

Review of various formulation and packing development, technology transfer documents like but not limited to Master Formula, Master Formula Card, Product Development Report, Dissolution Development report, Elemental Impurity Risk Assessment Report, Stability plan, QbD based Risk Assessment report, Failure Mode Effect Analysis, Process Validation Protocol

Use technical knowledge to perform in-depth review of API drug master file as per current US FDA expectations; identify deficiencies and formulate strategies to resolve them. Close coordination with Packaging material and Excipient vendors, placing orders, arranging technical documents to Analytical and Regulatory teams.

Finished, Stability Section, knowledge of Instrument - HPLC, GC. Preferably know-how of Chromeleon Software.

After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

Junior Research Fellow to work under the research project entitled Wastewater to biofuel and bio products : Cyanobacterial bio refinery through a green circular bio-economy.

Candidate who can have good command in English language, Reading, Writing, Speaking.

Looking for a Research Scientist to join our dynamic research and development team. As a scientist, you will assist with research and formulation of final products. This role is an excellent opportunity for someone looking to develop expertise in formulation research and development.

HPLC, GC, IC method development, feasibility, verification, equivalency, validation for API, complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated & India markets

Experience in analysis of Solid Oral - FP, In-process or Stability samples. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation, Transfer Solid Oral. Experience of GC, ICPMS and or LCMS operation.