Masters degree in biomedical sciences, medicine, biotechnology, bioengineering or related field with a strong track record from bachelor throughout master.
Global contract development and manufacturing organization (CDMO) Lonza has announced a major expansion of its highly potent active pharmaceutical ingredient (HPAPI) and payload-linker manufacturing capabilities at its Visp, Switzerland facility. The investment aims to strengthen the company's integrated support for the rapidly growing antibody-drug conjugate (ADC) market.
Glenmark Specialty S.A, a wholly owned subsidiary of Glenmark Pharmaceuticals Ltd. (Glenmark) announced the advancement of its multi-country Phase 3 clinical trial for Trastuzumab rezetecan (SHR-A1811), a HER2-targeted antibody drug conjugate (ADC), for patients with platinum-resistant ovarian cancer (PROC).
PESU Institute of Pharmacy is organising 7th International Conference on Translating AI into Healthcare Practices on 18 & 19 September 2026 at the PES University, EC Campus, Bengaluru. It is a multidisciplinary conference for Engineering, Medical, Nursing and Pharmaceutical Sciences.
Doctorate (PhD/MD/MS/MDS) or equivalent degree OR having 3 years of research, teaching and design and development experience after MVSc/MPharm/ME/MTech
BSC (nursing) in experience in Pediatrics/ OBG, GNM, BSc/ Bcom/ B pharm /BE Familiarity with smartphones and data file management. Willing to work in chitradurga district.
Bachelors Degree in Life Sciences / Genetics/Genetics Counselling with minimum 03 years relevant experience. OR Post Graduate Degree in Genetic Counselling.
Post Graduate degree (MSc) in Life Science/Chemistry/Biochemistry /Biotechnology or equivalent selected through a process described through any one of the following : a. Scholars who are selected through National Eligibility Tests – CSIR- UGC NET including lecturership (Assistant Professorship) or GATE.
The Sr Manager is accountable for ensuring regulatory compliance, driving operational excellence, and enabling strategic transformation of literature review processes, including screening, quality management, search strategy governance, systems, and ancillary operations.
Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness
Responsible for identifying and developing new business opportunities in Pharmaceutical Contract Manufacturing (CMO), Loan License Manufacturing (LLM), and R&D services for USA, CANADA, EU, UK and ROW Market.
Perform analysis of ointment, cream, gel, solution, raw material, and stability samples. Hands-on experience with HPLC, UPLC, GC, UV, IR, pH, viscosity, and assay testing.
This role focuses on managing post-approval regulatory activities, including variations, renewals, and compliance with country-specific requirements. You will partner with cross-functional teams to ensure timely submissions and maintain regulatory dossiers.
Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world.