Ph.D. in a science or engineering subject or MD, MS, MDS in medical science subject or ME, MTech, MPharm, MVSc with three years R&D experience as on the last date of application, evidenced from RAship or associateship or from date of registration of PhD.
Masters degree in Life Sciences, Biological Sciences, Allied, Pharmacy. and Two years experience in research and development in academic, industrial institutions.
Ph.D. in Biotechnology, Life Sciences with at least two years of research experience in zebrafish biology. Experience in performing zebrafish experiments and skills in molecular biology are required.
M.Sc, M.Tech in Microbiology, Biotechnology, Life Science with 4 years of Research experience of OR Doctoral degree in life science, Environmental science. OR Doctoral Degree in life science.
Experience in pharmaceutical research, experimentation, and data interpretation based on analytical results. Proficiency in laboratory techniques, equipment handling, and GMP knowledge.
Vendor Management, Contract testing laboratories qualification, Qualification and management of contract vendors and external service providers, QMS and compliance.
Experience in New Development, Product Life Cycle Management associated with regulatory function. Well versed with Product Development, Manufacturing and Sterility Assurance, Deficiency Management.
Centaur Pharmaceutical is the largest specialty of drug manufacturing Organization. We provide high quality affordable medicines trusted by healthcare professionals like USFDA and MHRA.
Health Sciences, Health Care Professional degree required e.g., BSc, MS, PhD, RN, BSN, MSN, NP, RPh, B.Pharm, Pharm D Advanced degree preferred. Minimum 7-12yrs of Pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities
Oversee and ensure all EMIA/APAC Regional PV Operations Hub Key Performance Indicators are completed in a timely manner, with high quality, and in compliance with worldwide regulatory and Global PV requirements.
Eugia Pharma receives a warning letter from FDA which summarizes significant violations of Current Good Manufacturing Practice (CGMP) regulations for finished pharmaceuticals.
U.S. Food and Drug Administration (FDA) inspected a drug manufacturing facility of Eugia Pharma Specialities Limited (Unit III), at Patancheru (Mandal), Sangareddy, Hyderabad, Telangana, from January 22 to February 2, 2024. It is a wholly owned subsidiary of the Aurobindo Pharma.
Indoco Remedies receives final ANDA approval from the USFDA for Lofexidine Tablets 0.18 mg with Competitive Generic Therapy designation, It is a generic equivalent of Lucemyra Tablets, 0.18 mg of USWM, LLC.
Institute of Nano Science and Technology, Mohali, Punjab, an autonomous institution of Department of Science and Technology, Government of India, has been established under the umbrella of NANO MISSION, initiated by DST to boost research and development in the field of Nanoscience and Nanotechnology in India. INST started its activities on 3rd January 2013, the date on which its first Director was appointed.
Ph.D., Masters degree, Bachelors Degree with First class in all the preceding degrees in the appropriate branch of Pharmacy, with an exemplary academic record throughout.
Government Primary Health Centers Government Medical College Hospital, Ariyalur and District Health Office, (Government Primary Health Centres) are inviting applications for the following vacancies on daily wages and salary basis under the National Health Group Scheme in Ariyalur District under District Siddha Medical Division.
The candidate should have a Masters degree MS, M.Pharm, M.Sc preferably in any stream of Pharmaceutical sciences preferably in pharmaceutics and pharmaceutical analysis. Candidate age should not exceed more than 28 years on the last date of the application.