Medreich facilities have received the seal of approval from leading global regulatory bodies such as -UK MHRA, Australia TGA, SA MCC, Health Canada, and French AFSSAP, GCC, PIC, regulatory bodies of various countries in the African continent and independent bodies like UNICEF and MSF
Executive FORMULATION DEVELOPMENT
Carrying out the Literature search on APIs, patents, excipients, technologies for the development of Solids (Tablets. IR. DR & ER dosage forms & Capsules Powder and Pellets filled)
Should independently carry out the Formulation R&D and scale up activities. Experience m handing equipments like RMG. Fluid bed driers & Granulators, size reduction miBs. Blenders, compression, coating & capsule fiHing machines. Preparation and review of Stability. Scale up. Process validation protocols and reports. Specifications (Raw material. Packaging material & product) etc. Compilation, review and interpretation of product development results, drawing conclusions and way forward in formulation development. Sufficient knowledge of regulatory guidelines (EU. US & Emerging Markets) and requirements. Good Documentation Practices. Compilation of Hold time study reports. Product Development Reports. Quality overall summary (QoS). QbR for dossier preparation. Co-ordination with cross functional teams for the timely completion of assigned activities.
Candidate Profile
M Pharma (Pharmaceutics) / PhD with 2-8 years Experience
Date : 24th June 2017
Time : 9 00 am. -1 00 pm
Venue : Medreich Limited (R&D-Genovo)
Plot No 36. Bommasandra Industrial Area. Anekal Taluk. Bommasandra.
Bangalore - 560 099. Karnataka
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