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August 2024

 

 

academics

 

Clinical research courses

Vacancy for Project Staff under externally funded Projects at IITR

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.
Aurobindo Pharma looking for Formulation Research Associates, Scientists - M.Pharm Apply
Experience in pharmaceutical research, experimentation, and data interpretation based on analytical results. Proficiency in laboratory techniques, equipment handling, and GMP knowledge.
Enzene Bioscience's Walk-in Drive for M.Pharm, MSc, MTech in Quality Assurance, Bio-Bulk Manufacturing
Vendor Management, Contract testing laboratories qualification, Qualification and management of contract vendors and external service providers, QMS and compliance.
Job for M.Pharm in Regulatory Affairs at Anthea Pharma
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 Hiring Research Associate
Centaur Pharmaceutical is the largest specialty of drug manufacturing Organization. We provide high quality affordable medicines trusted by healthcare professionals like USFDA and MHRA.
Work as Senior SERM Scientist at GSK
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
Work as Pharmacovigilance Manager at Teva
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 warning letter from FDA

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 ANDA approval from USFDA for Lofexidine

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.

Career for Ph.D or M.Pharm, MSc, MTech as Research Associate at Institute of Nano Science and Technology

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.