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.
Expertise in Virus Propagation, Cell-Culture, Protein Purification, Immuno-analytical Methods, Microbial Fermentation, Molecular Biology. Experience in human vaccines development is a plus.
The purpose of the Quality Medical Reviewer role in Medical Affairs is to review and approve medical and promotional materials to ensure they are medically accurate and interpreted correctly based on the review of references, citations and data available.
D.Pharmacy, B.Pharmacy, Pharm.D ; Must be registered with Telangana Pharmacy Council. However, applicants can register their certificates with Telangana Pharmacy Council as on date of their application and should upload this certificate online.
Post graduate Degree or PhD in Life Sciences, Pharmacology and Biomedical engineering with experience three years in conducting large scale intervention studies.
National Institute of Pharmaceutical Education and Research (NIPER - Raebareli) is an autonomous body which has been established under the aegis of the Department of pharmaceuticals, Ministry of Chemicals and Fertilizers, in the Government of India, to provide leadership in pharmaceutical Sciences and other related areas. It admits students for M.S (Pharm), programmes in Medicinal Chemistry, Pharmaceutics, Pharmacology & Toxicology, Regulatory Toxicology and Biotechnology every year.
D.Pharm, B.Pharm. Candidates with Typing and Computer skills will be preferred. Appointment will be given only for pharmacists who have registered in the Tamil Nadu State Pharmacy Council and who have completed one year trainee ship in the Department of Pharmacy.
The candidates should possess M.Sc Life sciences, Toxicology, M.S. Pharm. or M.Pharm. in Pharmacology or Pharmacology and Toxicology, Biotechnology PG degree in other relevant branches of life sciences.
PhD, M.Sc, M. Tech Biochemistry, Biotechnology, Life sciences with 2 - 8 years hands-on experience in protein purification techniques like centrifugation, depth filtration, lab scale column purification, ultrafiltration, diafiltration.
Doctoral Degree in Biochemistry, Public Health, Human Genetics, Hematology, Molecular Biology, Biotechnology along with a minimum 5 years of experience in research projects involving population screening, and inherited disorders.
Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics. Globally renowned, vertically integrated pharmaceutical player engaged in Research and Development (R&D), manufacturing, and marketing of high-quality chemical and biologic medicines across diverse therapeutic areas.
Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting.
Prepare and compile DMFs in compliance with regulations for regulatory and semi-regulatory countries. Provide necessary documentation support to the Marketing department.
Market research and analysis of CDMO landscape, Biologics, Biosimilars and Small Molecules business. Refer databases, news, articles etc and generate leads for potential business, newer technologies etc. Reach out to leads and present about One Source Capabilities.