Macrophage infection experiments, Cell biology experiments, Immunofluorescence, Western blotting, RT PCR and Cloning. IISER Berhampur, Odisha

M.Sc. in Biochemistry/Biotechnology/Molecular Biology/ Zoology with 60% marks or equivalent CGPA. IASST, Assam

PhD in Life sciences/ Biostatistics. Experience in Research and Development related to Biomedical Sciences.  ICMR, Headquarters

BSc / Msc in Life Science or B.Pharm / M. Pharm. with Post Graduate Diploma in Clinical Research (PGDCR) or MSc Clinical Research

Master’s degree from a recognized University/Institute in Life Sciences/Agricultural Science/Biotechnology or allied subjects; alternatively, the specified Master’s degree with selection through CSIR-UGC-NET/GATE or relevant national-level examinations conducted by Central Government departments/agencies. BRIC-NABI

Doctoral Degree in Biotechnology / Microbiology / Life Sciences. As per norms of the funding agency for research projects. North-Eastern Hill University, Shillong

Masters degree in Biochemistry/Biotechnology/ Microbiology from a recognized university with minimum four years research experience or PhD in Biological Sciences from a recognized university. IASST, Guwahati (Assam)

In this role you are required to solve routine problems, largely through precedent and referral to general guidelines

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations in its WHO GMP approved production facility and GLP qualified stringent quality control.

Supervising in aseptic area and exposure of machine qualification activity will be added advantage. Zydus Lifesciences

Hands-on experience with OSD process development equipment. Knowledge of ICH, BCS, and QbD principles. Experience in development, pilot, and clinical batches in a GMP environment. Piramals Discovery Solutions

Otsuka Pharmaceutical India Private Limited is primarily manufacturing IV and parenteral nutrition products across multiple markets and therapeutic segments.

Bachelors degree in pharmacy, life sciences, or a related field. Basic understanding of pharmacovigilance principles and regulatory guidelines is desirable but not required; relevant training will be provided. ICON plc

Advanced degree in Engineering, Biomedical Engineering, Life Sciences, Regulatory Affairs, or a related field. Demonstrated experience supporting regulatory submissions, registrations, compliance activities, and regulatory lifecycle management. Medtronic

Applications are invited for the above positions having the relevant experience as GLP study director/study personals in reputed CRO companies.

Write CMC regulatory dossiers for Drug Substance filing (small and Large API Molecules) using source documents, ensuring accuracy, completeness, and compliance.

The Medical Information Specialist (MIS) position is part of the ProPharma Medical Information Contact Center and follows all corresponding regulations, industry standards, and client/internal policies regarding medical information and the collection and documentation of adverse events, special situation events, and product complaints.

Aurobindo Pharma Limited has announced that the United States Food and Drug Administration (USFDA) has classified its Raleigh plant in North Carolina, USA, as Voluntary Action Indicated (VAI) following an inspection conducted at the facility in 2025. The Raleigh plant is owned by Aurolife Pharma LLC, a wholly owned step-down subsidiary of Aurobindo Pharma Limited, and is established for the manufacturing of inhalers, dermatology and transdermal products.