Ph.D, MD, MS, MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc, M.Pharma, ME, M.Tech with at least one research paper in Science Citation Indexed journal.
Masters in Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelor’s degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement.
Masters in Natural or Agricultural or Pharmaceutical Sciences, Animal Sciences OR Bachelor degree in Engineering or Technology or Medicine from a recognized University or equivalent
M.Sc, M.S. Pharm.,M.Pharm. in Biochemistry, Microbiology, Biotechnology, Life Sciences. Minimum CGPA of 6.75 for General category, OBC, 6.25 for SC. ST, 5.75 for persons with disability candidates on a 10 point scale in the qualifying examination.
Masters in Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelor degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement
Masters Degree in Science with specialization in Biotechnology, Genetics and Plant Breeding, Molecular Biology, life sciences from a recognized University or equivalent.
Torrent Pharma, the flagship Company of Torrent Group is one of the leading pharma companies of the Country. The Company was a pioneer in initiating the concept of niche marketing in India and today is ranked amongst the leaders in therapeutic segment of cardiovascular (CV), central nervous system (CNS), gastro-intestinal (GI) and women healthcare (WHC). The Company also has significant presence in diabetology, pain management, gynaecology, oncology and anti-infective segments.
Execution and review of Qualification, Re-Qualification and Validation activity of Equipment, System, Facility and Plant utilities.
Preparation and review of Validation, Qualification protocol and report.
Batch release and associated documents - preparation and review. Understanding of QMS elements and IPQA. Internal and external Regulatory team coordination.