Haryana

Regional Centre for Biotechnology (RCB) is an institution of national importance established through an Act of Indian parliament by the Department of Biotechnology, Govt. of India under the auspices of UNESCO. The primary focus of RCB is to provide world class education, training and conduct innovative research at the interface of multiple disciplines to create high quality human resource in disciplinary and interdisciplinary areas of biotechnology. To this end, the Centre is offering the master's and doctoral degree programs in biotechnology, while other degree/diploma programs in niche areas of biotechnology are under development.

The Centre invites applications from suitably qualified, dynamic, and result-oriented scientists with flair for teaching, to fill up the following academic positions on direct recruitment / deputation or contract basis. The candidate should preferably have demonstrated research experience, and interest to pursue research and teaching in any of the following areas: (1) Synthetic Biology & Metabolic Engineering, (2) Fermentation, Scale-up & Downstream Processing, (3) Biocatalysis & Enzyme Engineering, (4) Metagenomics & Microbiome, (5) Antibody Engineering for Therapeutic Applications, (6) Cancer Biology & Therapy, (7) Infectious Disease Biology for Developing Prophylactics and Therapeutics, (8) Plant Biotechnology for Crop Improvements, and (9) Big Data Analytics, Computational Biology & Bioinformatics.

NATIONAL BRAIN RESEARCH CENTRE (NBRC) invites application for the position of “Junior Research Fellow (Project)” in DBT funded project entitled “CRISPRI system: A toolbox to investigate novel regulatory mechanisms of synapse formation by long non-coing RNAs”.

Over the years Sentiss Pharma (erstwhile known Promed group) has positioned itself as the No 3 Ophthalmic Company* in Russia and has expanded its foothold in the US and European markets.
Our key competitive advantage lies in having the R&D center together with the world class manufacturing facility that has enabled us to provide end-to-end solutions from product development to marketing. Our manufacturing facility at Nalagarh (India) is EU GMP certified and TGA (Australia) approved.

Clinical Development Services Agency (CDSA) has therefore been formed as a not-for-profit society to provide supportive and focused environment to host world class clinical translation through a collaborative network of clinical investigators and premier research institutions.  It will tend enterprises, particularly SMEs involved in new technology innovation, to facilitate translation of scientific know-how into viable products for public health diseases like malaria, tuberculosis and dengue among others.

Post : Senior Research Officer (Zinc Sepsis Study)

Clinical Development Services Agency (CDSA) has therefore been formed as a not-for-profit society to provide supportive and focused environment to host world class clinical translation through a collaborative network of clinical investigators and premier research institutions.  It will tend enterprises, particularly SMEs involved in new technology innovation, to facilitate translation of scientific know-how into viable products for public health diseases like malaria, tuberculosis and dengue among others.

Post : Clinical Research Associate

Established in the early 90's, this organization has emerged as an integrated pharmaceutical company offering products to the global market. Headquartered at Delhi NCR, India and plant in North India, the Company develops, manufactures and markets a wide range of quality products in diverse area of treatment.Over the years, the organization has positioned itself as a significant player in the Russian and CIS markets and has expanded its foothold in the US, Europe, India and other markets. The key competitive advantage lies in having the Research & Development centre together with the world class manufacturing facility that has enabled it to provide end-to-end solutions from product development to marketing. The manufacturing facilities are approved by many regulatory bodies including EUGMP and WHOGMP thereby allowing the company to reach International markets.

Post : Senior Research Scientist - Product Development

Indian Drugs and Pharmaceuticals Limited (IDPL) is a Central Public Sector Undertaking wholly owned by the Government of India engaged in manufacture of pharmaceuticals with plants at Rishikesh, Gurgaon & Hyderabad and two Subsidiary Units at Chennai and Muzaffarpur. IDPL was established with main objective of creating self-sufficiency in respect of essential life saving medicines, to free the country from dependence on imports and to provide medicines to the millions at affordable prices and not to make millions from the medicines. IDPL was basically conceived and established as a part of Healthcare Infrastructure and has played a pioneering infra-structural role in the growth of Indian Drug Industry base. Recently, the Company has entered in the field of OTC as well as Surgical Products.

Clinical Development Services Agency (CDSA) is an extramural unit of Translational Health Science and Technology Institute (THSTI) and has been established as a not-for-profit society to provide cost affective, high quality preclinical and clinical product development support services to meet the country’s growing healthcare needs. It will tend enterprises; particularly SMEs involved in new technology innovation and facilitate translation of scientific know-how into viable products.

Post : Research Officer (iKMC Study), 01 Position

Established in the early 90's, this organization has emerged as an integrated pharmaceutical company offering products to the global market. Headquartered at Delhi NCR, India and plant in North India, the Company develops, manufactures and markets a wide range of quality products in diverse area of treatment.Over the years, the organization has positioned itself as a significant player in the Russian and CIS markets and has expanded its foothold in the US, Europe, India and other markets. The key competitive advantage lies in having the Research & Development centre together with the world class manufacturing facility that has enabled it to provide end-to-end solutions from product development to marketing. The manufacturing facilities are approved by many regulatory bodies including EUGMP and WHOGMP thereby allowing the company to reach International markets.

Post : Senior Executive/Asstt. Manager- Regulatory Affairs