Thorough understanding of Quality Control investigations, including Lab Incidents, OOS, and OOT. Relevant experience in Oral Solid Dosage formulations and / or Active Pharmaceutical Ingredient processes.

Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world.

You will be embedded in our client's study team and have a dedicated ICON line manager to support you. Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports

Provide technology delivery leadership and domain expertise for Biological Studies product teams that enable in silico, in vitro and in vivo experimentation. Partner with Research and Technology leaders to create technology delivery strategy and prioritized agenda for Biological Studies.

Masters degree in pharmacy, life sciences, pharmaceutical management with relevant experience in the biopharma, healthcare, or market research sector is required.

U.S. Food and Drug Administration approval of a New Drug Application for KHINDIVI hydrocortisone Oral Solution as a replacement therapy in pediatric patients five years of age and older with adrenocortical insufficiency.

GSK plc announced that the US Food and Drug Administration (FDA) has approved Nucala (mepolizumab) as an add-on maintenance treatment for adult patients with inadequately controlled COPD and an eosinophilic phenotype.

Ph.D. from a recognized University in subject Pharma, Chemistry, Biochemistry, Biotechnology. Level 11 of Pay Matrix Rs.67,700-2,08,700, 7th CPC Scale.

The applicant needs to attend the Walk-in-interview on the scheduled date & time. Any delay will not be entertained any point of time.

To conduct situational analysis and field visits for enabling informed decision by the states in implementation of the initiative. To assist states and MoHFW in adoption, customization of the IT based Inventory Management system developed by CDAC and NIC e.g. e-Aushidhi, DVDMS etc.

PhD, MD, MS, MDS or equivalent degree or having 3 years’ experience of research, teaching and design and development experience after MSc, ME, M.Tech with at least one research paper in a Science Indexed (SCI) Journal

M.Tech., M. S.c., M. S. in Biomedical Engineering, Medical Devices, Bioelectronics, ECE, EEE, EIE, Instrumentation, Mechanical Engineering, Life Sciences, Pharmaceutical Science with a consistently good academic record.

Professionals having proven competency and success in their area of specialization, with at least 1 years of post-qualification experience and should possess minimum M.Sc / B.Tech / BE /MCA / MPH / B.Pharm/BAMS/ BSMS/ MD in AYUSH or equivalent qualifications in relevant subject.

Master degree in Life Sciences Molecular Biology, Biotechnology, Microbiology, etc. from a recognised university or equivalent. Candidates with prior experience in molecular parasitology and molecular biology techniques involving gene cloning and protein purification will be preferred.

Ph.D. in life sciences, Biological sciences, Botany, Plant Sciences, Biotechnology, Biochemistry. Experience in using tools and techniques of plant molecular biology, plant genetic transformation and Plant genome editing as evidenced by publication in peer reviewed journal.

Will be responsible for overall administration of Ind-CEPI activities at THSTI. This will involve coordinating the construction and usage of shared infrastructure facilities at THSTI, leading regional networking and capacity building with LMIC’s and CEPI support from the Project Management Unit in oversight of the RFPs selected for funding etc

Institute of Nano Science and Technology, Mohali invites applications from prospective candidates with independent source of fellowship for admission to its Ph.D. Programme in the following three units Energy Environment unit, Quantum Material and Devices unit, Chemical biology unit. 

M.Pharm, B.Pharm, MSc ; Environmental Monitoring activities in a sterile/aseptic manufacturing facility. Conduct and supervise non-viable particle monitoring and line clearance operations.

M.Sc in Chemistry, B.Pharma ; Analysis of Raw Material / Finished Product / Intermediates / Stability / Sampling.