Life Sciences

The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.

As an Associate Global Scientific Advisor, you will Provide timely, accurate and credible scientific and medical input for a variety of projects pertaining to scientific communication around Novo Nordisk’s products. Collaborate closely and communicate effectively with various cross-functional stakeholders including colleagues from the US affiliate, global medical affairs, and other functional areas. Engage in dialogue with Key Opinion Leaders (KOLs) in different settings with focus on medical and scientific information. Prepare presentations for Novo Nordisk standalone events and international medical congresses.

Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.

You will be responsible for executing or assigning in-process activities during shifts, conducting line clearances, material verification, overseeing start-up of machines, and coordinating sampling activities to ensure product quality and compliance.

Support the Quality vision and mission for Amgen India aligned with Amgen’s mission to serve patients. Support Amgen India Quality Team Lead in the development and implementation of a multi-year Quality technological plan aligned with Amgens standards and overall strategic imperatives.

Development of a nanostructured graphene oxide, polydopamine coated PDMS nano-biosensor monitoring GPC1 for the early diagnosis of pancreatic cancer.

Identification of key regulators and their controlling Mechanism in a combinatorial amyotrophic lateral sclerosis Network : an integrated bioinformatics analysis. Experience in computational tools, Network Biology, Molecular modeling and Simulation, Knowledge of computer programming languages with good command in oral and written communication skills in English will be given preference.

Ph.D. in Biotechnology, Life Sciences or any of the allied subjects. For the first position, research experience in cell culture techniques, transfections, and biochemistry and molecular biology is required. Prospective candidates with experience in malaria parasite biology, chimeric mouse studies and other infectious diseases shall also apply.

Phase 2 Pilot Study to test the efficacy of Ayurvedic oral cannabis preparation in the peri-operative Period in oral cavity squamous cell cancer. Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, etc with PG Diploma in Clinical Research is mandatory, with one year experience in relevant filed is preferred.