Walk in interview in FORMULATION DEVELOPMENT at Medreich | M.Pharm

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

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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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