VIVEK MORRIS PRATHAP

same as aforementioned

• Developed and maintained courteous and effective working relationships with sport federations at national and international level.
• Used strong analytical and problem-solving skills to develop effective solutions for challenging situations in case of collection of dope samples from athletes.
• Managed whereabouts failures of athletes and well versed in drafting notice to athletes.
• Deals with Therapeutic Exception for Use applications for those need according to their medical condition.
• Audited "Khelo India Games 2023" in Bhopal, Indore and Jabalpur.

• To build a database of Head_Neck Cancer and Lung Cancer radiology and pathology images linked to their clinical information.
• To annotate images and make annotations available as part of the database.
• To establish mechanisms to facilitate access to the database.
• To drive the AI based algorithm/application development using the Biobank infrastructure and data along with infrastructure.
• To jointly develop the website and the data portal.
• To jointly conduct training/ outreach program & popularize the Imaging Biobank.

• Handling and maintenance of animal cell line (suspension and adherent cell line).
• To carry out Biological testing of Therapeutic monoclonal antibodies and In-vitro potency assays for Therapeutic Monoclonal antibodies viz. Rituximab, Trastuzumab, Adalimumab, Pembrolizumab, Aflibercept, Natalizumab and Bevacizumab.
• Capillary Electrophoresis (CE-SDS[R & NR], CZE, cIEF)
• High Pressure Liquid Chromatography (SEC, CEX)
• Method Verification/Validation for the products which received first time in the laboratory.
• Participated in team-building activities to enhance working relationships.
• To contribute as part in Internal Audits of Laboratories, external audits being carried out by NABL, Drug Regulatory Authority and WHO.
• To carry out Intermediate checks of Equipment and coordinate with the vendors visit for its AMC program and calibration at regular intervals.
• Preparing SOPs and Work Instructions for various Q.C. Parameters of Biologicals being tested in laboratory and equipment’s respectively and other necessary administrative requirements for product testing Laboratories.
• Handling and preparation of schedule and plans for Internal Audits.
• Handling compliance to non-conformance for Corrective & Preventive Actions (CAP) and it verifications.
• Handling documentation of Inter collaborative studies with different Biologicals Testing Laboratories/ Manufacturer’s across India.
• Contributing as part in activities related to the implementation of ISO 9001: 2015, ISO 14001: 2015 & OHSAS 18001: 2008 standards.