About the Company :
Biophore started in 2007 as a generic industry, currently with 70 DMF files across EU,US & Canada, with 50 patents filed and 20 products in pipeline. The company has 2 US-FDA approved API facilities and 1 EUGMP approved solid oral manufacturing facility.
The portfolio of Biophore spread with 30 therapeutic segments with specialized oncology medications and diagnostic media. Company having state of art technology facilities with infrastructure from conceptualization to regulatory submission. The R & D centers is established in 80,000 square feet work place with advanced technology in hand to produce cost effective medicines.
Produces wide variety of products with vast scope of reducing diseases and available to all people. Their mission is to have continuous improvement and inclusive work culture with customer satisfaction is the DNA of Biophore.
About the Job
Experience : 1-5 years with Masters in Pharma
Location : Hyderabad / Secundrabad
Salary offered : 2-7 LPA
Roles
Timely preparation of Development strategy notes for Formulation development and obtained Data compilation (Formulation, Analytical & Stability) and interpretation during development work.
Planning and execution of R&D trials.
Ability to conduct the Pre formulation & Stability studies for development trail batches and Formula and process optimization by mini pilot batch manufacturing.
Plan and perform the Stability studies in different packing systems as per ICH guidelines.
Coordinating with the external and cross functional departments of AD, QA, QC and Production for the smooth
execution and Optimization of both the formulation and process variables for development of stable drug product comparable with the reference product.
Timely Implementation of QbD based approach and related advanced versions in product development and Preparation of LSR, DSR, DER, BOM, MFR, and PDR.