• Planning and execution of formulation development activities such as development batches, scale up batches and GMP batches.
• Interpretation of test results, compilation and report writing.
• Preparation of formulation development, stability protocols and reports.
• Sending weekly report about projects to Clients.
• Able to participate and conduct telecon with Clients.
• Preparation and review of SOPs, EOPs, ECCs, Guidelines, etc.
• Maintenance of laboratory note books as per SOP.
• Maintenance of all facility documents and project specific documents as per SOP.
• Coordination with other support teams like Stores, QC, QA, Engineering etc.
• cGMP document preparation such as BMR, BPR, etc.
• Strict adherence to Quality compliance as mentioned in SOPs and lab systems.
• Any other task assigned by team leader or HOD.
Qualification : M.Pharm
Location : India
Industry Type : Pharma
Functional Area : R&D
End Date : 15th June, 2018
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