Applicants must be licensed to practice pharmacy in a State, the District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States.
Knowledge of the methods and procedures involved in the proper handling, dispensing and storing of pharmaceutical materials; Knowledge of basic labeling, measuring and weighing devices; Ability to take accurate arithmetical computations; Ability to understand and carry out oral and written instructions; Ability to keep accurate records; Ability to lift and move heavy objects.
The conference is aimed to highlight the latest developments in the field of drug discovery & development and health care. The program will feature discussions on various aspects of pharmacy like drug discovery, pharmaceutical industrial revolution, artificial intelligence, digital transformation with technological changes, pharma engineering and clinical research. The meeting will bring together the senior executives of pharma industry and academicians paving the path for a high-level strategic deliberations that will help in shaping the future of the drug discovery, and research.
Conclave - Drug Industry, Medicine, Discovery Research and Regulation Good Manufacturing Practices : Opportunities and Challenges of Revised Schedule M
Assist in management of Biotechnology laboratories. Maintain and coordinate use of scientific equipment and infrastructure. Preparation of scientific reports. Maintenance of data-bases. Preparation of technology related policies, IPR and legal issues. Perform any other duties assigned to him, her by the Executive Director from time to time.
Candidates having a Ph.D degree in Life Sciences, Biotechnology, Plant Molecular Biology or having three years of research experience after MV.Sc, M.Pharm, ME, M.Tech with good academic record and research experience in plant molecular biology field with at least one research publications in peer-reviewed SCI journals.
Project Research Scientist conducts monitoring visits for assigned trial protocol and trial sites. Overall responsibilities are to ensure that the trial is being conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
First Class Post Graduate Degree, including the integrated PG degrees in life sciences, biotechnology, biochemistry, Applied biology. Second Class Post Graduate Degree including the integrated PG degrees with PhD in life sciences, Applied biology, biotechnology, biochemistry.
Comparative analysis of two different techniques for evaluation of HLA gene haptotypes in patient with celiac disease. Post graduate degree in any branch of Life Sciences, Biochemistry, Biotechnology, Molecular Medicine or allied sciences with strong academic record.
Candidates having Ph.D. degree in Life Sciences, Biotechnology, Molecular Biology or a related field or having M.Tech. in Biotechnology, Bioinformatic with three years of research experience and one research publication.
Masters degree in Natural Sciences or Bachelors Sciences in Engineering or Technology or Medicine from recognised University And, OR Scholars who are selected through National eligibility tests CSIR-UGC NET including lectureship or GATE or selection process through National level examinations conducted by central government department and their agencies and institutions.
Management and performing periodic observation of retain sample & identified the deviation through periodic observation. Review of Temperature, RH data in retained samples area.
Should maintain R Vs C Vs A metrics with actuals and Gap and shall populate the data with all CFT in weekly meet.
Should be able to handle procurement plan through SAP with good knowledge to carry out MRP process in SAP, knowledge of Kinax is will be additional advantage.
The Regulatory Affairs Manager II is fully proficient in applying established standards and performs regulatory affairs management for moderately to highly complex international market submissions in all regions with minimal coaching. They are expected to facilitate strategic input, provide proactive contribution to submission planning, identify areas for continuous improvement, and lead cross-functional activities. They participate in the continuous improvement of processes and tools, systems.
Ph.D. in Science, Engineering, Technology, Veterinary Science, Pharmacy. Candidate must possess certificate, marksheet of basic knowledge of Computer from training institute or should have results with computer as a subject in degree or diploma curriculum from Government approved University or should have passed 10th or 12th examination with computer as a subject as prescribed by GAD in Government Resolution
MSc. with 1st Class in Genetics,Human Genetics, Life Sciences, Biochemistry from recognized university and suitability bases on CSIR, UGC, ICMR, DBT, etc.