Life Sciences

Master Degree in Biotechnology, Biochemistry from a recognized university. Research / working experience in regulatory framework, and having the experience of handling small laboratory animals, etc. Analysis of Micro- Nanoplastics in food matrices; Micro and Nanoplastics as emerging food contaminants : Establishing validated methodologies and understanding the prevalence in different food matrices

Post Graduate degree in Life Science, Pharmacy, including the integrated PG degrees. Candidate with a Ph. D degree with specialization in Pharmaceutics, Pharmacology and Toxicology, Biotechnology, Life Sciences, Pharmacy and or significant experience in the formulation and development of nanotechnology-based drug delivery systems, clinical research, In vitro and In vivo models and molecular biology. 

The candidate will be responsible for performing a range of wet-lab based analyses, which include routine semen analysis, sperm DNA Fragmentation Index assessment, Y-chromosome microdeletion testing, RNA extraction, DNA extraction, protein extraction, PCR analysis, and ELISA assays. These tasks will be carried out as part of the broader study objectives, ensuring high standards of accuracy and consistency.

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.