Ph.D./MD/MS/MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc/M. Pharm/ME/M. Tech with at least one research paper in Science Citation Indexed journal.

Candidates with a master degree in Chemistry, Chemical Sciences, Pharmaceutical Chemistry with excellent academic record. CDRI-Research Internship Program supported by Cipla Foundation

M.Sc. in Biotechnology/ Biochemistry/ Microbiology/ Zoology from a recognized University or equivalent. Knowledge of the basic molecular and microbiology techniques

Candidates having a doctorate degree in Life Sciences or equivalent with a good publication record and fulfilling the norm/guidelines of DST Office Memorandum number DST/PCPM/Z-06/2022 dated June 26, 2023 are eligible to apply.

Post Graduate degree in Microbiology or Molecular Biology or Virology or Biotechnology from any Govt, recognized University. 

Post-graduate degree in Microbiology, Biochemistry, Laboratory Hematology, Laboratory Medicine, Anatomy, Physiology, Dermatology, Hematology, Radiotherapy, Endocrinology, Ophthalmology, Oncology, or any other clinical / paraclinical specialty/Superspecialty

First-class Masters degree or integrated masters degrees in Life Sciences, Biotechnology, Biochemistry, Molecular Biology, Genetics, Zoology from a recognized University.

Post Graduate Degree Biotechnology, Physics, Biochemistry. Collection of fresh glioma tissue from the Neurosurgery theatre and subjecting it to snap-freezing.

Masters Degree in Natural Sciences / MVSc or bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent; and 2 years of experience in Research and Development in Industrial and Academic Institutions or Science and Technology Organisations and Scientific activities and services.

B.Sc./M.Sc./B.Pharm/M.Pharm Chemistry ; Analytical Method Validation RM/PM, SPEC/STP/Protocol & Report Preparation

B.Sc, B.Pharma & M.Sc with relevant experience, Compression, Granulation, Coating, Stability/ FP / HPLC/ CC

To drive end-to-end execution of new product launches for assigned geographies, ensuring timely delivery, commercial success, and alignment with revenue targets.

Blister & Bottle Packing, Liquid Manufacturing Filling, Sachet filling. Diploma, BSc, B.Pharm, M.Pharm

Experience in granulation, compression, capsule & coating oral liquid manufacturing areas of regulated markets. FDA approved personnel in tablet manufacturing would be preferred.

Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift.

Pharma domain. Experience with different data assets, sales reporting/commercial analytics team in healthcare/pharma/life science would be a plus

Must have broad understanding of the development of pharmaceutical products, regulatory and patent law globally. Patent and regulatory databases in different countries

Line clearance during dispensing of raw material and packing material. QA Verification during dispensing of raw material and packing material.

Lead Commissioning, Qualification & Validation activities for equipment, utilities, and computerized systems. Develop & approve IQ, OQ, PQ, cleaning validation, process validation, and CPV documentation.