M.Pharm, B.Pharm, M.Sc, B.Sc. Experience of QC documents, Specification and STP Preparation. Experience of method development, method validation and documentations
To facilitate the Change Controls to be logged for various reasons. To initiate the Change Controls due to revision in BMR / BPRs and other PD related changes
Prepare, compile, review, and submit product registration dossiers in CTD I eCTD format as per country-specific requirements and EAEU Unified Registration Procedure.
Evaluation of regulatory documents, compilation of dossier and submissions to CDSCO-HQ/CDSCO-Zonal offices for regulatory approval of drug substance and drug products.
Macleods is one of the fastest growing pharmaceutical company, having strong presence in various therapeutics segments. Ranked amongst the top 10 companies.