To work on project entitled Biobanking in Multiple Myeloma. Graduation or Post Graduation degree in Science with PG Diploma in Clinical Research is mandatory.

The scheme supports high level innovation in Life Sciences and related areas and is not meant for basic research projects.  Supports post proof‐of‐principle, prototype, process optimization/ product validation aimed at affordable product, process development addressing societal needs. 

HPLC, GC, IC method development, Validation and Transfer for API, complex OSD, complex generics products like long acting injectables, nasal sprays, peptide injections, peptide OSDs, oncology and Topical products etc using various analytical technique. Expertly in peptide characterization. Well versed with USP/EP/BP/IP and various current regulatory guidelines ICH/ EMEA/ FDA Hands on experience on Nitrosamine and Genotoxic impurities method development, M.Pharm / M.Sc

Should demonstrate a strong understanding of B2B business dynamics and have independently managed and traveled across these regions. A solid grasp of business contracts, along with excellent negotiation skills, is essential.

Execute the production planning in Liquid manufacturing block and ensure the production plan achievement as per plan. Responsible to ensure the entry and exit, gowning and personnel hygiene procedures are followed in liquid manufacturing block.

possess a Bachelors degree and a Post-graduate degree in Pharmacy, with first class or equivalent either in Bachelors Degree or a Post-graduate degree obtained from any of the Universities or an Institution established or incorporated by an Act of the Parliament or State Legislature in India or any other educational institution recognised as such by Government or an institution declared to be deemed as University under section 3 of the University Grants Commission Act, 1956

Development of antibiotic nano formulation for the prevention and treatment of udder infection in dairy animals. First class in M.Pharm with specialization in Pharmaceutics, Drug Delivery Technology, Pharmaceutical Technology or equivalent from a recognized University. GPAT. GATE. NET qualified.

Possess a post-graduate degree with first class in the appropriate branch of specialization in Pharmacy, as may be specified by the Government, the educational qualification shall have been obtained from any of the Universities established or incorporated by or under the Central or State Act in India, or any other educational institution recognized as such or deemed as a University under section 3 of the University Grants Commission Act, 1956 or possess an equivalent qualification recognized as such by the Government

Centre of Excellence on Phytopharmaceuticals and Herbal Products; Ph.D. in Pharmaceutical Sciences or Analytical Chemistry, Pharmaceutical Analysis with first class post- graduation in M.Sc. Analytical Chemistry, Organic Chemistry or M.Pharm, MS.Pharm Pharmaceutical Analysis, Quality Assurance, Natural Products, Medicinal Chemistry; Hands on experience for operation and analysis of HPLC and different chromatographic instruments.

To provide technical, regulatory, liaison, administrative and organizational support within the Incubator, working in conjunction with incubatees, innovators and researchers; Ph.D. in Life Sciences / MBBS / First class in BTech / M.Sc degree in Life Sciences. Experience in business management, or management of the intellectual property, or project management.

Pragmatic strategies for the delivery of phytodrugs across BBB through plant derived exosomes for the management of neuroinflammatory diseases. Experience mammalian cell culture, toxicological assessments, molecular techniques PCR, Western Blotting, immunoassays, and neurodegenerative disorders preferred. Knowledge of animal handling, and neurobehavioral techniques like Open field and Morris water maze also preferred.

The ideal candidate should be proficient in working with mouse brain, mammalian and stem cell culture, as well as basic and advanced molecular biology techniques such as cloning, transfection and epigenetic analysis. Additional skills include confocal, fluorescent microscopy. Masters degree in Science from a recognised university

Potential stemness genes knockout through CRISPR- Cas9 technology in triple-negative breast cancer cells via multitalented nano-hybrids. Experience in CRISPR-Cas9 gene editing system, Animal cell culture, RT-PCR, In vivo, Animal handling, Nanoparticle synthesis and characterization, SELEX technique. Willingness to enroll in the PhD programm at ARI. Post Graduate in Biotechnology/ Life Science. 

Applications are invited from in-service contractual employees working under NHM in the same post in other districts of Odisha to fill up various posts under NHM Nabarangpur district. Fresh candidate need not apply.

In this role, the Senior Scientist-I will work on isolation, purification of known and unknown impurities, compounds by preparative HPLC and characterization of molecules using various analytical technique. Prepare, execute, and complete IQ/OQ/PQ of new instruments. Indent the required glass ware, chemicals, and columns for the ARD projects.

Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies

Seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other groups. Master degree in pharmacy/ life science/Biology/Biotechnology/ Biochemistry/Diploma in Clinical Research

Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system.