January 2026

Masters degree in Biological Sciences with expertise in Molecular Biology and Genomics. Hands-on experience in basic laboratory protocols and techniques like DNA extraction, quality check, qPCR, sequencing.

To support for commercial troubleshooting/remediation/Market complaints for Non-Oral manufacturing sites. To support for timely investigation/execution and to resume commercial manufacturing and to meet market/ sales requirement.

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

Dissolution apparatus, GC, IR and AAS and Documentation related to QMS. To review respective GMP Documents of QC department such as analytical / worksheet of In Process and Finished Product.

M.Pharm/B.Pharm/M.Sc/B.Sc Review of BMR/BPR and process validation reports, in process testing, sampling and line clearance, Media Fill. Emcure

clinical data cleaning and reconciliation activities performed with high accuracy and in accordance with GCP, SOPs/WPDs, and study protocols. experience in RAVE / Veeva EDC

Post - graduate in Science / B.Tech / M.Tech / M.Pharm with experience of working (PhD will be considered as 4 yrs experience) in R&D, Working in Govt research scheme

Diploma (State Paravaidyak Certificate of registration with Council is mandatory)

Masters / Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences / MVSc / Animal Sciences. Doctoral Degree in Science / Pharma.