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4.0 - 8.0 years
0 Lacs
gujarat
On-site
As the leader of the DQA department, your role is to ensure the implementation of CGMP rules and regulations in Research & Development. Your responsibilities include: - Reviewing the Lab validation Protocol and Report of CRD. - Reviewing the Process Development report for DMF filing. - Reviewing the Specification and STP of Key Raw Material, In-Process, Intermediate stage, and Finished Product. - Reviewing the Method Development Report, Method Validation Protocol/Report, Method Transfer Protocol of ADL. - Reviewing the stability protocol and Report. - Preparing SOP, Formats / Annexures, Log books, and ensuring RA and GLP Compliance. - Interacting and communicating with R&D, ARD, QA, and Regu...
Posted 1 month ago
5.0 - 10.0 years
7 - 12 Lacs
Vadodara
Work from Office
Experience in Literature search, Process Development, Lab Validation and Documentation as per regulatory requirement, should be aware of characterization
Posted 3 months ago
5.0 - 10.0 years
3 - 8 Lacs
Vadodara
Work from Office
Responsibilities: * Develop processes through lab validation * Conduct R&D synthesis with API focus * Collaborate on miscellaneous industry projects * Ensure compliance with safety standards Annual bonus Provident fund Office cab/shuttle
Posted 3 months ago
3.0 - 8.0 years
3 - 6 Lacs
Bharuch, Ankleshwar
Work from Office
Review the Lab validation Protocol and Report of CRD Review of Process Development report for DMF filing. Required Candidate profile Lead the DQA department to implement CGMP rules and regulations in Research & Development.
Posted 5 months ago
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