vacancies

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.

M.Sc in Plant Biotechnology, Biochemistry, Botany, with Three Years Research Experience OR Doctoral Degree in Biotechnology, Biochemistry, Botany. Experience of working in plant tissue culture and transformation, molecular biology techniques and plant genome editing.

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.

Develop strategy to configure, distribute, and collect, and review and approve, high quality country specific and or site specific documents or essential regulatory documents and any updated or amended regulatory documentation.

Project Managers provide business and technical leadership for one or more projects within a business unit, leading project teams through the identification, justification, prioritization, initiation, development and implementation processes. This Sr. Specialist position will act as a Project Manager leading commercial launches in US and Global markets within the Pharmaceutical Business segment.

First class Post Graduate degree including the integrated PG degrees such as MS Pharm, M.Pharm, M.Tech Pharm or with specialisation in Pharmaceutics, Pharmaceutical Technology Formulation Drug delivery or equivalent. 

Evaluation and submission of application on online portal for getting domestic manufacturing and marketing permission from DCGI. Evaluation and submission of applications on online portal for import registration, import license of drugs and medical devices in India. 

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.

Ph.D degree in relevant field and first class or equivalent at either Bachelors or Masters level in the relevant branch. AND Minimum of 10 years of experience in teaching, research, industry out of which at least 3 years shall be at a post equivalent to that of an Associate Professor.