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.
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.