Post-Graduate degree in any branch of life sciences from a recognized University with atleast three years of post- qualification research experience in the field of biochemical and molecular biology.
Developed, implemented, and managed GMP quality systems to ensure regulatory compliance and Production operational. Continuous quality improvement Initiatives, driving enhancements in processes, product quality, and operational efficiency.
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.
M.Sc. in Natural or Agricultural Sciences, M.Pharm, MSc in Botany, Chemistry or Life Science or Bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent
The Regulatory Affairs and Policy Advocacy division within the Biotechnology Industry Research Assistance Council facilitates innovators in navigating regulatory approval pathways and advocates for policies impacting startups, SMEs, and young entrepreneurs.
Engineering M.Tech, M.Pharm in Life Sciences and related fields. OR Medicine : MBBS, BVSc, MD OR Design : M.Des. OR Business : MBA with Life Sciences or Engineering Minimum Two years of prior work experience related to medical discipline of our mentioned thrust areas on website.
Graduation in Science B.Pharm, Life Sciences. Biotech, Zoology, and Botany with PG diploma in Clinical Research with interest in monitoring of interventional clinical trials.
Masters Degree in Life Sciences, MVSC, Engineering or Medicine from a recognised university or equivalent With at least 1 years of R&D experience in academic institution or relevant industry with NET & GATE Hands-on experience in cell culture
Doctoral degree in science or masters degree in engineering or technology from a recognized University in a relevant discipline. Proteomics of medically important snakes of North-east India and development of diagnostic assays for the identification of snake bite at species level
Bleachers, Masters degree or equivalent in communications, journalism, public relations, science communication, or a related field.
PhD or additional qualifications in biotechnology or life sciences preferred.
PhD in Biology, Chemistry, Biotechnology or related fields. Relevant professional experience at the international level in public health management of antimicrobial resistance or related fields. Previous experience in infectious, communicable diseases or Biological Safety Levels 3 facilities would be advantageous.
Seeking a highly skilled and motivated Vaccine Formulation Scientist to join our innovative R&D team. The role involves designing and optimizing vaccine formulations, focusing on stability, immunogenicity, and scalability for various delivery platforms.
Bacterial Endotoxin testing for routine samples, and regular water testing. Analytical method validations related to the BET, MLT, and Bioburden testing. Plate reading for different microbiological analysis. Daily Observations of the sterility test canisters, tubes.
Hands-on experience in Handling of Granulation, Compression, Coating, and Capsule Filling equipment. Hands-on experience in Blister Packing and Bottle Packing areas.
Jodas is a Global, specialty, innovation driven, emerging, generic bio- pharmaceutical company, that is asserting itself among the worlds foremost pharmaceutical companies.
AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.
Post : International Associate Regulatory Affairs Director I
M.Pharm, M.Sc, Pharm.D candidates who completed a Diploma course in clinical research and with at least three-year experience in handling clinical trials