JOB RESPONSIBILITIES To support ISBU through new and renewal dossier submission, pre-registration recommendation response preparation and share with Customer for new and renewal dossier submission, update dossier as per post approval change...

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To assure Quality and cGMP compliance of the products being manufactured and Packed for Cephalosporin Block. • To review MMD-I / BPR and release of the batches for further processing stage like Granulation, compression, coating, inspection,...

Name Ashish Shah Level Function: Purchase Sub Function Capex / Projects Location: Bhat Estimated total of direct and indirect reports 4 Reporting to (Administrative Manager) HOD - Purchase Reporting to (Functional Manager) HOD - Purchase Ma...

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"• Ensure the c-GMP Compliance and schedule M compliance in production. • Ensure the completion of production targets with zero quality issue. • Ensure the compliance of inspection /Audit in coating area and follow of procedures/SOPs. • To ...

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Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator etc. by following test procedure. • To attend the training as pe...

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"Aseptic Filling : • To plan daily Manufacturing activity per norms of cGMP. • To supervise Vial decartoning, Vial washing, Vial Sterilization, Vial filling and packing activity as per requirement in Cephalosporin block. • To check cleaning...

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To perform the in process checks for control on production for the process / product being manufactured. To ensure Quality and cGMP compliance of the products being manufactured. Parenteral Manufacturing : • To give Area /Equipment clearanc...

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Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Procedur...

Planning and Execution of all MMD-I & BPR preparation activity pertaining to Main Pharma Block, Cephalosporin Block, Penicillin Block & Rifampicin Block of Dholka, as well as Contract Manufacturing & Herbal. • Preparation and review of MMD-...

"• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Proce...

"• Compliance to cGMP and other regulatory requirement. • To perform the daily packing activities in central packing department in accordance with cGMP norms. • To execute packing as per the plan. • Ensure and maintaining proper housekeepin...