M.Pharm

Ph.D. with first class or equivalent grade at the preceding degree in the appropriate branch with very good academic record. Preference will be given to the candidates having Post Graduate Degree in Pharmaceutical Analysis.

Post Graduate Degree, including the integrated PG degrees or PhD. Experience in clinical research or public health research, Hands-on experience with data.

Looking for candidates with relevant experience in Injectable regulated plant for Manufacturing, Packing & Store & Warehouse Department at SEZ Matoda Location

Specifications, Method Validations / Transfers, Investigations, Audit Trail, Stability, Batch Release, Analytical, Molecular & Bioassay Techniques.

Invoice Entries, Billing Entries, take care of material weighing, go down Stock checking. Loading, Unloading Checking, Handling of storage checking and issuing of material from Go down.

Analytical method development of finished dosage forms. Stability studies of finished dosage forms. Analytical method validation Analytical method transfer.

Strong knowledge of country-specific labeling regulations and guidelines across the US, EU, Canada, Australia, and Switzerland, combined with hands-on experience in label development, including CCDS, USPI, and packaging components. 

The Manager, Regulatory Affairs – CMC is responsible for developing and implementing regulatory strategies related to Chemistry, Manufacturing, and Controls (CMC) for pharmaceutical or biologic products.

Qualification of equipment & Documentation, IPQA, QMS-Ohange Control CAPA, Deviation, Process Validation, Cleaning Validation, APQR, Audit Compliance.