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Candidates should have experience in Formulations regulated manufacturing company such as USFDA & MURA, EU with audit exposure.

Method Development, Method Validation, Method Verification of DS, DP as per In -House and monograph methods. Testing of analytical samples by using HPLC, GC, Dissolution, AAS, Titrations, Wet analysis.

Pre formulation studies of Pharmaceutical & Medicinal Devices and to check the compatibility of the API with different excipients. Formulation development of Pharmaceutical & Medicinal Devices

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.

B.Pharmacy, M.Pharmacy; ROW Market. Collaborate with Cross-Functional teams. Market Analysis. Conduct Market Research to understand industry Trends. Excellent Communication & Problem-solving skills. Data Management.

Candidates with hands on experience with Stability, finished products analysis of formulation products will be given preference. Handling of batch manufacturing and filling activity with regulatory exposure 3 Piece, BFS eye drops and Injectable in Sterile area. 

M.Pharm; Responsible for development and execution of complex injectable, suspension, emulsion, ophthalmic formulations solution, emulsion for regulated markets. Should be responsible for review of trials and stability data throughout product development.

To ensure timely completion of analysis and data completion for the same. To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems. M.Sc / BPharm or any relevant degree

Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coating, Capsule filling, Primary Packing and Secondary Packing. Expertise in e-BPR and e-log will be added advantage. 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.