Faculty who can successfully execute R&D and consultancy will be considered. Faculty who can promote patents, Industry Interaction, and other value-added courses will be preferred.

Must have worked in regulated plants having approvals of USFDA, MHRA. etc. Hands-on experience in handling and implementing cGMP Current Good Manufacturing Practice practices and Good Documentation Practices

Execute Analytical method Validation activities of drug substances API by using HPLC,GC and Spectroscopic techniques as per regulatory guidelines. Execution and coordination for Analytical method transfer activities of drug substances.

This project will involve cloning, expression and purification of recombinant proteins and their biophysical characterization. Cell culture and animal model experiments. Synthesis and characterization of small molecules.

Expertise in the synthesis of inorganic and hybrid halide materials. Expertise in single crystal growth and solving crystal structure. Extensive research experience in the field of Materials Chemistry.

Targeting Malaria Parasite Heme Synthesis – A New Intervention Strategy for Malaria Transmission, Liver stage Prophylaxis and Relapse . Ph.D. in Biotechnology, Life Sciences or any of the allied subjects. Research experience in cell culture techniques, transfections…

A Phase 3, Multicenter, Open-label, Rater-blind, Active-controlled Study to Evaluate the Efficacy and Safety of Bedaquiline for the Treatment of Multibacillary Leprosy When Combined with Rifampicin and Clofazimine.

Ph.D. in any branch of Life Sciences. Prior experience in molecular biology techniques, cell culture assays, expression and purification of proteins, and cellular signaling are required. Hands-on experience with X-ray crystallography or cryo-EM is preferred…

The Technical Consultant will work as a Project Manager, driving implementation of key schemes including the Departments Production Linked Incentive schemes by effectively liaising between the Project Management Agencies, scheme participants, the Department…

Centaur Pharmaceuticals one of the rapidly growing Pharmaceuticals Company in India. Centaur Pharmaceuticals is USFDA and MHRA approved plant is seeking deserving candidates having experience working in Oral Solid Dosage Manufacturing facilities for regulatory…

Analysis and processing of In process and Finished product and handling of HPLC, UV, FTIR, K/F, AAS, IC, Dissolution. Analysis of Raw material and Excipients and handling of HPLC.

D-Pharmacy or B-Pharmacy. Registered with pharmacy Council Certificate. The minimum age is 18 years and the maximum age is 46 years in terms of G.O.Ms.No.30 dated 08-02-2024 of General Administration Department, Government of Telangana.

Timely compile documents for license renewals, update and re-registrations. Review of technical documents like BMR. Stability protocol & report, specification and method of analysis, process validation protocol and report required for dossier compilation.

HLL Lifecare, a Schedule B, Mini Ratna Central Public Sector Enterprise under the Ministry of Health and Family Welfare is Indias leading manufacturers and marketers of Contraceptives, Healthcare and Pharma products and services.

Contribute to preparation including authoring where relevant and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and/or regional perspective.  Good understanding of regulatory guidelines…

RM, PM, FG, Dispensing, Dispatch, Documentation. After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

M.Sc, M.Tech Zoology ,Medical or Human Genetics, Biochemistry, Molecular Biology, Botany, Microbiology, Biotechnology, Life Sciences, Applied Biology, Cytogenetics. Candidates should have minimum six months experience in Cytogenetics

Candidate with project management experience in Discovery Sciences along with Commerical or Product launch, Product strategy experience would be preferred; should be adept at managing project milestones, budget and stakeholders.

General injectable, Sex Hormones, Cyto Parenteral, SKID, QMS, GMP Documentation. Sun Pharma is the fourth largest specialty generic pharmaceutical company in the world.