3-4

Demonstrating a good degree of competence in regulatory affairs and understanding of dossier technical requirements within the region, this role provides technical subject matter expertise to support Country RA teams with their local publishing and agency submission transmission needs.

A Phase-lV, single-arm, multicentric study to assess the safety of SIIPLs qHPV vaccineCERVAVAC when administered in a two-dose schedule to girls and boys aged 9-14 years and in a three dose schedule to women and men aged 15-26

Dossier and document preparation as per CTD,ACTD and country specific guidelines, Review of dossiers, DMF and Technical documents, Answer query raised from regulatory authority, package insert, SmPC, PIL & MSDS preparation

M.Pharm / M.Sc. jobs; Analysis of Finished product, Method development, validation, Documentation as per GLP Stability analysis of finished products, calibration of instruments

Assists Head-Bioanalytical in the smooth running of the bioanalytical section through efficient project and quality management in conformance to GLP guidelines.

B.Pharma, M.Pharma - IPQA; B.Tech, B.E Any stream in Nutraceuticals, Chemical, Pharma devices, Pharma equipments, FMCG, API, Packaging.

2-6 Years of experience in Finished Product, RM, QMS, Stability and AMT, AMV

M.Pharm, B.Pharm, M.Sc; RM, Stability, In-process, FG, AMV and AMT, QMS, AQA, IPQA, Validation

B.Pharmacy, M.Sc, M Pharmacy ; IPQA, QMS, Validation, AQA, Stability, RM, IP, FP, Granulation, Compression, Coating, Packing