Pharma Jobs

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.

To create an awareness regarding antibiotic resistance. Postgraduate degree in basic science or graduate/ post graduate degree in professional course

Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy, safety profiles to support on-label prescribing for appropriate patients.

Bachelors, Master degree or PhD in science, math, engineering or related discipline; The Principal, Regulatory Affairs, Intelligence, Materials is expected to perform with minimal supervision and is an experienced and detail-oriented professional with expertise in materials and with an understanding of the interplay of materials and medical devices, pharmaceuticals and combination products.

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

M.Pharm, M.Sc, M.Tech Bioinformatics, Pharmaceutical Chemistry or Biotechnology. Experience in Molecular Modelling, Computer-aided drug design, ML, AI skills with experience in various tools

B. Pharm, B.Sc. for BA BE and For clinical B. Pharma or M.Sc. Or M.B.B.S.B. V. Sc. and A.H is compulsory. M. V. Sc. Pharmacology and Toxicology is desirable for preclinical; Check CROs for conducting preclinical/ clinical/ bio equivalence studies by site feasibility/ selection visits or evaluation for ensuring adequate facility, skill and experience for conducting the studies as per requirements

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