Amneal Pharmaceuticals, Inc is a global pharmaceutical company. Our team of 7,500+ colleagues helps make healthy possible through the development, manufacturing, and distribution of a diverse portfolio of 270+ high-quality medicines. Amneal is a global essential medicines company powered by a robust U.S. generics business. Amneal is a growing branded business with deepening portfolios in institutional injectables, biosimilars and select international markets including India.
Sun Pharma is the fourth largest specialty generic pharmaceutical company in the world. We provide high-quality, affordable medicines trusted by healthcare professionals and patients in over 150 countries.
MSc, M.Tech, M.Pharm. in relevant stream of Biological Sciences with 3-5 years of relevant experience in Analytical R&D, QC department of Biopharmaceutical industry.
Analytical Method Development of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical Method Validation of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray.
Accountable for regulatory transition activities to achieve relevant project turning points, as well as core business development operational activities including but not limited to running the green light process, preparation of documentation and risk, issue management.
As Regulatory Professional, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. Further responsibilities include Life Cycle Management.
BS, RN, MS, PharmD in life sciences or equivalent relevant scientific qualifications or professional training. Generate and file data for signal detection and safety data review. Demonstrated understanding of global pharmaceutical drug development and lifecycles.
Bachelor of Pharmacy from any institute approved by Pharmacy Council of India, AICTE. Master in Pharmacy, Masters in Pharmaceutical Technology M.Tech Master of Science in Pharmacy; Price Monitoring and Resource Society Unit under State Drug Control Directorate.
Overcoming the Inflammatory Cascade in Neonatal Sepsis, a Nanomedicine Approach. First class post-graduate PG degree including integrated PG degree such as M.S. Pharm, M.Pharm, M.Sc, M.Tech or Equivalent with specialization in Pharmacology & Toxicology, Regulatory Toxicology, Biotechnology, Life Sciences.
M.Pharm/ME/M.Tech; Lignin valorization via biomaterial development, depolymerization and green technology; project funded by Government of India at Institute of Nano Science and Technology, Mohali. Research experience in Tissue engineering/ Biomaterials / Synthetic Modification of biopolymers/ Proficiency in animal handling is preferable.
M.Sc. or M. Pharm. or M. Tech. in Basic or Applied Sciences, Engineering or related areas. Students who have appeared for the final year, semester examinations are also eligible, provided that the degree will be granted by the time of joining. WALK-IN-INTERVIEW FOR Ph.D. - August 2024 SESSION
Assistant Professor Pharmaceutical Management recruitment at NIPER; Ph.D. with 1st Class or equivalent at the preceding Degree in an appropriate branch with a good academic record throughout and at least 5 years of teaching/research, industrial experience with published works of high quality
Masters degree in Life Science / Biochemistry / Biotechnology / Molecular Biology / Botany or any other branch of life science are eligible to apply. Genetic dissection of 13-lipoxygenases to modulate JA biosynthesis for enhanced N, P, K deficiency tolerance in rice
Bachelors or Masters degree in Pharmacy, Pharmaceutical Sciences. Lead and manage the technology transfer of pharmaceutical formulations from R&D to manufacturing Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs
Bachelors or Masters in Pharmacy. Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave, Isolators and Lyophilization.
M. Pharm / M. Sc / B. Pharm / B. Sc; Experience in Method Validations and Verifications, Analytical Method Transfers with Brazil Regulatory exposure. Experience in Finished Product, In-Process, Stability and GLP activities