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.
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.
M.Sc Chemistry from a recognized University, Institute.
Sound knowledge of marker analysis by HPTLC and HPLC. Method development and validation by HPTLC and HPLC
Skills of drafting, editing of scientific documents/ articles, technical reports etc.
Method validation, verification and transfer to Quality control lab for OSD and PFOS formulations. Development, optimization and validation of analytical methods to support OSD formulation ANDA.