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.
A masters degree on a point scale wherever the grading system is followed with Ph.D. in a concerned, relevant, allied subject from an Indian University or an equivalent degree from an accredited Foreign University.
Ph.D. degree and First class or equivalent at either Bachelors or Masters level in the relevant branch. At least two successful Ph.D. guided as Supervisor, Co-Supervisor and minimum 8 research publications in SCI Journals, UGC, AICTE approved list of Journals
Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.
Infusion bags processing activities, In-process checks and Line Clearance activities, Handling of shift activities and manpower. Preparation of QRM, Incident and Investigation, OOL and OOS investigation, CC and CAPA, Protocols and CAPA closure reports.
UC Riverside scientists have developed a nanopore-based tool that could help diagnose illnesses much faster and with greater precision than current tests allow, by capturing signals from individual molecules.
An inter-departmental research team at the LKS Faculty of Medicine of the University of Hong Kong has conducted the world’s first analytic real-world cohort study on the association of clozapine, a highly efficacious antipsychotic drug, with the incidence of blood cancer.
Diploma in Pharmacy from a recognized Institution and registered as Pharmacist under the Pharmacy Act, 1948. Bachelor Degree in Pharmacy from a recognized Institution and registered as Pharmacist under the Pharmacy Act, 1948.
M.Sc, M.Tech, Biotechnology, Life Sciences, Botany, Zoology, Biotechnology, Microbiology. Having hands on knowledge in animal cell culture, molecular and cellular biology work.
Graduate in Life Science or B.Pharma. P.G. Diploma in Clinical Research is mandatory. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India.
M.Sc. in life sciences with NET, DBT-JRF, INSPIRE, GATE or equivalent exam cleared. Minimum 60% marks in Masters or equivalent degree. Hands-on experience in basic molecular biology techniques such as DNA & RNA isolation, protein purification, routine PCRs and cloning is required.
Masters degree in Science from a recognised university and 2 years research experience in a laboratory setup. Who studies brain development in health and disease. 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.
Experience in Yeast Biology not limited to culture methods, strain modification, transformation and expression studies. Experience in Molecular Biology and Biochemical techniques, preferably in Saccharomyces Biology.
Demonstrated success in project management & experience with mentoring and coaching junior team members. Ability to act independently with a solutions-oriented and balanced approach to the grey areas.
Good exposure require in IPQA - OSD and Sterile, Qualification OSD and Sterile. Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.
Responsible for guiding and coaching employees, monitoring their productivity, and overseeing regular equipment safety and maintenance. Responsible for performing batch execution in Sterile Injectable lines manufacturing and packaging.
Provides the labeling, artwork strategy, regulatory intelligence and knowledge which are required to develop, market, and maintain products. Provides strategic labeling input and support for global development projects and, or marketed products