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B.Pharmacy / M.Pharmacy; Candidate should have Injectable experience and sound knowledge on manufacturing and packing activities of liquid and Lyo products. Aseptic process simulation, process validation, cleaning validation, Batch records review and batch release.

Diploma in Pharmacy from a recognized Institution and registered as Pharmacist under the Pharmacy Act, 1948 and Two years experience as Pharmacist in any recognized Hospital or Pharmacy after registration as Pharmacist under the Pharmacy Act, 1948.

B.Pharm with minimum 01 year of experience OR D. Pharm with minimum 03 years experience. Experience in Dispensary, Pharmacy of the Hospital having minimum 200 beds. Candidate should be prepared to work in shift duties, including night shift. Registration with State Pharmacy Council with duly allotted Registration Number is mandatory. Experience of working on computerized system desirable.

Knowledge of FDA, cGMP, ICH, DMF guidelines for regulatory submissions. Hands on experience in CMC submissions, supplemental applications. Experience working on labels will have added advantage. Excellent written and verbal communication skills; experience in Regulatory Affairs of Finished dosage formulations mainly for USFDA, EU. M Pharmacy / M. Sc. / B Pharm

M.Pharm / B.Pharm / M. tech / B. tech / B.E. / B.sc / Diploma / ITI; Tablet, Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. HPLC, GC, IR, UV, Dissolution and other QC Equipment, QC Method Validation and Transfer.

Bachelor of Pharmacy; Exposure in Pellets, Hard Gelatin Capsules, Soft Gelatin Capsules & Packing in OSD Formulation Manufacturing. Exposure in Pellets, Hard Gelatin Capsules, Soft Gelatin Capsules, Tablet & Packing

Surveillance of Foodborne Disease Pathogens in North-East India under funding of ICMR, Govt, of India. M.Sc in Life Sciences plus three years research experience in Microbiology.

To work on project entitled Biobanking in Multiple Myeloma. Graduation or Post Graduation degree in Science with PG Diploma in Clinical Research is mandatory.

HPLC, GC, IC method development, Validation and Transfer for API, complex OSD, complex generics products like long acting injectables, nasal sprays, peptide injections, peptide OSDs, oncology and Topical products etc using various analytical technique. Expertly in peptide characterization. Well versed with USP/EP/BP/IP and various current regulatory guidelines ICH/ EMEA/ FDA Hands on experience on Nitrosamine and Genotoxic impurities method development, M.Pharm / M.Sc