Hyderabad

GCP Subject Matter Expert, Provide independent and objective quality advice in support of clinical trial activities and in line with current standard methodology. Experience in Quality Management, Quality Assurance. pharmaceuticals

Master or PhD of pharmaceutical. Perform statistical analyses of data from the laboratories using R and possibly other languages SAS or standard statistical software used in Sanofi, JMP, SIMCA, internal tools. Sanofi

Masters in life sciences. Certifications in Incubation and Entrepreneurship, Regulatory Affairs, Business Models, Digital Marketing. Centre for DNA Fingerprinting and Diagnostics

Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts, Clinical Research Associate at Sun Pharma

Your responsibilities include authoring process validation protocols and reports, conducting risk assessments, utilizing tools like Continued Process Verification (CPV), PAT Tools, and statistical analysis tools

Must have an Experience in Method Development & Method Validations. Should have Exposure on HPLC, GC, GC-HS, LC, LCMS, UV,IR

Masters Degree in Pharmaceutics or Pharmaceutical Sciences from a recognized university. The candidate will be eligible to apply for the Ph.D. position next semester. PhD candidates are encouraged to apply.

Line Clearance, Batch records review, Online Process Monitoring, Investigations, Audit Trail, Recipe Review, Risk / Impact Assessments, Material Managements DS Shipments.

M.Pharmacy/ B Pharmacy/ B.Tech. Having Injectable Experience in filtration, Filling, Sealing, Stoppering, Garment Washing, Vial Washing, Autoclave, Ophthalmic, Suspensions, Lyophilizes. Operations and Training. Aspiro Pharma