Sound knowledge of analytical method development and Method validation using HPLC as per guidelines. Knowledge of calibration and operations of all equipment like balance, ph meter, in analytical operation.
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
Responsible to perform, review the investigations arising from incidents, out of specifications, out of trends, product failures, market complaints to identify the root cause and implement appropriate corrective and preventive actions.
The MSL recognises and communicates feedback and insights of strategic importance from their interactions with scientific experts to better inform Lilly's strategic direction for research and commercialization.
M.Pharm or M.Sc. in Chemistry, Biochemistry, Pharmaceutical Chemistry, Sciences with five years research experience. PhD in Chemistry / Analytical Sciences / Instrumentation / studies related to tobacco and tobacco products.
Masters degree in Pharmacology from a recognised university, Institute with 2 years of experience in pharmacological studies of Drugs, Research, Testing laboratory.
Systems medicine approach to tackle the problems of early diagnosing and prognostic stratification of mycosis fungoides. Post Graduate Degree in Basic Science OR Graduate, Post Graduate Degree in Professional Course.
The candidates should have PhD degree Botany, Life Science, Biotechnology, Biochemistry, Biosciences, Plant Science, Plant Molecular Biology or any related Held from Indian University, Institutes with NIRF ranking of upto 20 overall or in respective arears or those who have done PhD from abroad will be eligible.
B.Pharm, M.Sc, M. Pharm with 3-8 years of experience in IPQA and manufacturing, packing QMS related activities in oral solid dosage form tablets, capsules, soft gelatin capsules, pellet Dosage form manufacturing facilities.
As a Senior Specialist, Expert Medical writer , you will support the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional/local levels. Independently prepares of clinical and regulatory documents such as Protocols, Clinical Study Reports, or Investigator Brochures.
Biological E. Limited started during a time when the nation sought access to critical healthcare products. Founded and led by Dr. DVK Raju, Biological E. Limited commenced its operations in 1953 as a biological products company manufacturing liver extracts and anti-coagulants.
Eminent College of Pharmaceutical Technology (ECPT), under the Eminent Group of Colleges, was set up by the Trust, Nirmala Foundation, West Bengal. The institute is approved by Pharmacy Council of India, New Delhi as well as affiliated to MaulanaAbulKalam Azad University of Technology, West Bengal, India. ECPT started its journey in the year 2017 with a purpose and mission of providing students of the districts and the peri-urban areas with high-quality pharmacy education.
B.Pharma with minimum 1-year experience OR D.Pharma with minimum 3 years working experience in Dispensary, Pharmacy of the Hospital having minimum 200 beds. Registration with State Pharmacy Council with duly allotted Registration Number is mandatory.
Post Graduate Degree Life Sciences from a recognized institution, university with two years experience in R&D, Academic, Science and Technology Institutions after obtaining essential qualification.
As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight.
M.Sc. in the field of Biology, Molecular Biology, Human Genetics, Cell Biology, Biochemistry, Microbiology. Candidates with UGC-CSIR, NET, GATE, ICMR-JRF, DBT-BET qualification will be preferred.
The position will be working in a matrix organization with extensive communication and collaboration with stakeholders from various functions within or outside Global Regulatory Affairs. The role will have to enable the preparedness of the employees to work on different projects and roles, to facilitate communication within the matrix organization, to ensure efficient and scalable resourcing supporting the business priorities.
Coordinate with cross functional teams e.g. Medical monitor, Regulatory Affairs, supply chain, statistics, Data management, QA and QC, CRO, vendors etc.Works cross-functionally and with external vendors to proactively manage the execution of the clinical trials