Diploma course in Pharmacy from an institution recognized by Government of India and the Pharmacy Council of India. Must have registered with Assam Pharmacy Council and should possess valid professional Pharmacist License. Minimum 02 years post qualification relevant work experience as Pharmacist.
Must possess D.Pharma, B.Pharma from recognized university and registered in the AP Pharmacy Council. If the applicant possesses an equivalent qualification to prescribed qualification in this notification, applicant shall enclose a copy of the Government orders to that effect to the application, failing which their application will be rejected.
PhD Chemistry, Biochemistry, Biomedical Engineering, Biology, Physics, Biotechnology, Computer Science, Information Technology, Life Sciences Degree Awarded, MD, MS,MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc, M.Pharm, ME, M.Tech with at least one research paper in Science Citation Indexed journal.
Phase Ilb, III study to determine efficacy of curcumin and metformin to reduce the incidence of second primary tumors of aero-digestive tract in patients with history of head and neck squamous cell carcinoma
M.Pharmacy in Pharmaceutics or M.Tech Pharm. Technology, 1-2 years of research, industrial experience in formulation and Development with research publication.
Ph.D in the area of biological sciences or equivalent. Experience in organizing scientific workshops for school children, delivering popular scientific lectures, articles on science in leading dailies etc.
Officers under the Central, State, U.T. Governments, Universities, Statutory Bodies or Autonomous Bodies or Research and Development Organizations Holding analogous posts on regular basis, or With 6 years regular service in the grade of Pharmacist Grade II in the Grade Pay of Rs. 2800
Act as a Project Lead for the assigned clinical trials while supervising CRAs in their functions of monitoring and administration of clinical trials. To manage service providers, CRO and Vendors, collect quotes budget proposals, summarize and present the same to the management team.
Working in aseptic process area for supervision and operation of filling and manufacturing activity. Handling of Complex of Microsphere formulation. Handling of Dry powder filling machine.
Knowledge of Production Planning, Co-ordination with Corporate Planning Team for smooth function, Scheduling of Manufacturing, Follow-ups with Inter-Departments for production activity.
M.Pharm, M.S Pharmaceutics, Pharmaceutical Technology, with GPAT, GATE, any National Eligibility test. Should have experience in formulation development of solid orals, semi-solids research. Experience in PAT tools, continuous manufacturing is highly desirable. Candidates with industrial experience will be given preference.
Graduation in Biotechnology or B.Pharmacy from Govt. recognized University and Boards. Computer course in office software.
Knowledge of Biostatistics. Research Methodology workshop training and Good clinical laboratory Practices
Project titled Phytopharmaceutical Mission. Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences Or Bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent
First Class Post Graduate Degree, including the integrated PG degree in Bioinformatics, Biotechnology, Computational Science, Pharmaceutical Chemistry, Computational chemistry or equivalent from a recognized university.
Masters in Life Science, Microbiology, Zoology, Earth Science, Biochemistry, Biotechnology, Bioinformatics, Clinical Research, Public Health etc. ENVIROENMENT AND OCCUPATIONAL HEALTH; prepare a comprehensive annual plan of activities/ work as well as Strategic Plan for the forthcoming year in consultation with the Programme Coordinator and will be responsible for implementing the same. The activities will include development of value added information products, conducting GSDP courses, organizing mega, regional events and other outreach activities.
Provide comprehensive statistical support across all phases of research studies, including clinical trials and epidemiological investigations, from design and sample size estimation to data analysis, interpretation, and reporting. Expertise in Clinical Research Methods, including study design, biostatistics, research ethics, and regulatory requirements.
responsible for overseeing day-to-day operations, ensuring compliance with regulatory standards, and driving continuous improvement across all processes. Oversee daily QC and microbiology operations, ensuring CGMP and regulatory compliance.