via Career pages·Yesterday
Research Associate
Cadila Pharmaceuticals
Full-timeOn-siteliterature reviewnew product developmentregulatory compliance
Location:Dholka, IndiaType:Full-timePosted:Yesterday
"JOB RESPONSIBILITIES
- Review of Literature summary report, patent summary report and development protocols.
- New product development, Planning and Resource allocation for Domestic, ROW, US, EU, CMO Market.
- Alternate source development for API and Excipients, GC improvement of existing products.
- Timely execution of scale up/ exhibit/process validation of allotted projects.
- Process improvement and troubleshooting of existing commercial products.
- Overall review of Formulation Development data during stage gate clearance.
- Execution of allotted projects in stipulated timeline & within budget.
- To check feasibility of manufacturing and costing of all new projects for UID.
- Timely review of LNB and project files for allotted projects.
- To coordinate with CFT team like AR Lab, Production, Manufacturing, QA/QC for timely
completion of project.
- Ensure timely address of regulatory deficiencies for Domestic, ROW, US, EU, and CMO Products.
- Compilation and review of the FnD data, interpretation and summarize the recommendations.
- Preparation and Review of technical documents such as MFC, SOP, PDR, TTD protocol, MMD, FPS and development protocol.
- Ensuring the availability of manufacturing and analytical requirements/documents and resources before execution of batches at plant.
- To evaluate the deviations noticed during technology transfer at shop floor and perform root cause analysis and rectification after consultation with the concerned department.
- Ensure adherence to guideline in various product development activities during development"
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