D.Pharm, B.Pharm. Desirable, Experienced candidates in hospital sector will get preference.  Registration Certificate issued by State Pharmacy Council. 

managing life sciences projects, preferably in the areas of bioprocess technology/ biotherapeutics/ biopharma. Proven track record of successfully coordinating interdisciplinary teams to deliver complex projects within scope and deadlines.

Research experience in Plant Virology, Molecular Plant Pathology, Molecular Biology and Biotechnology with knowledge of Computer and bioinformatics, NGS data analysis having high quality publications in SCI journal Higher degree in relevant subject and research experience All India Network Project on Emerging Pests AINP-EP-Sub component-1, Plant Virus- Identification and evolution of emerging plant viruses infecting economically important fruits, vegetables and legumes crops, diagnostics, interaction with hosts and management

Ph.D in Life Sciences, Applied Biology, Genetics, Biotechnology. Candidate having 01 year experience in Molecular Biology and or Immunology

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

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.

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. 

Qualification as per norms of UGC, State Govt, Concerned Regulatory Body. Pharmacology, Pharmaceutics, Pharmaceutical Chemistry, Pharmacognosy.

Bachelor of Pharmacy B.Pharma degree with at least 02 years of experience in AYUSH Hospitals, Clinics. In case B.Pharma candidate is not available, Diploma in Pharmacy D.Pharma candidates with at least 02 years of experience will be considered. Should have computer knowledge.

The Engagement shall be made through a process of Walk in Interview against Academic performance Index- 100 marks and Interview - 10 marks- Moreover, 5 marks wilt be given to the Degree holder in pharmacy, in addition.

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.