Rajnarayanan Seenu

About Rajnarayanan Seenu

11+ years of industrial experience in the Life Science domain which includes R&D and cGMP regulated environments from pre-clinical to the Manufacturing stage • Having experience in Design, Development, Configuration, and Support of BIOVIA Workbook (Accelrys ELN), BIOVIA Notebook (Contur ELN), LabWare LIMS, LabWare ELN• Having an overall understanding of Lab applications’ ecosystem as well as the integrations that can assist in tracking the end-to-end lifecycle of studies revolving around various groups, lessening human errors through automation projects, and improving data integrity and Quality Assurance.• Working knowledge in enterprise architecture of Lab Systems such as Labware LIMS, BIOVIA Workbook, and BIOVIA Notebook.• Preparing automated and ad-hoc Reports with the help of tools such as BIOVIA Pipeline Pilot, and SAP Crystal Reports• Coordinating with IT teams on activities such as Periodic Infrastructure Maintenance checks, Disaster Recovery tests, Infrastructure Migration, Root Cause Analysis, and Resolution of incidents• Participated in migration of Biovia ELN from On-Premises to Cloud (AWS) infrastructure• Having experience in Change management, Deviation management, and CAPA effectiveness checks using Change Management Systems like TrackWise and ServiceNow. • Good listening and communication skills with the capability to breakdown technical aspects of an issue into a more understandable form for regular business users• Closely collaborating with Developers, Business Analysts, and the Validation team throughout the Software Development Lifecycle and Validation Lifecycle to provide seamless and scalable solutions• Working knowledge of Document Lifecycle Management systems like Veeva Vault Quality Doc• Having experience in authoring Technical Design Specifications, Configuration Specifications, and Work Instructions. Also have experience assisting team to maintain Business Enabling Documents, Training Materials, Traceability Matrix, Installation, and Operation Qualification documents.• Good Understanding of FDA regulations that govern Computer System Validation. • Working knowledge of Lab Information Systems in regulated environments, FDA cGxP, and 21 CFR Part 11 regulations, cGxP Computerized System Validation• Having experience in training and leading 3-6 member teams in the Administration and Support of Lab Applications

Experience

1. R & d Info Systems Analyst Iii

   Gilead Sciences

   Jan 2023 — Present · Foster City, CA, US

   Responsible for installation, configuration and administration of BIOVIA Workbook product (formerly known as Accelrys ELN and Symyx Notebook)2. Providing ELN administration and technical support in a GMP regulated environment3. Providing end-user support including troubleshooting problems at the application level (includes working with vendors to resolve issues)4. Coordinating with Infrastructure, IT, and Database Administrators to ensure continuous system availability5. Interacting frequently with System Owner, Technical Lead, and Business Process Owners to provide technology solutions6. Developing strong relationships with vendor partners and staff to develop solutions7. Providing architectural solutions for interface developments8. Owning system configuration and oversee maintenance activities9. Ensuring system performance for large number of simultaneous users10. Participating in development of long-range system roadmap

Education

• Jawahar Hr Sec School, Neyveli

  Higher, Education-Computer science

  2005 — 2007

• St.Joseph's College of Engineering

  B.E, Electrical and Electronics Engineering

  2007 — 2011

Skills

• Mysql
• Plc
• Crystal Reports
• Biovia Eln
• Html
• Labware Lims
• Lims
• Javascript
• Jsp
• Labware Eln
• Java
• Sql
• Pl/Sql
• Hp Quality Center
• Oracle
• Requirements Analysis
• Microsoft Sql Server
• Openlab
• Lims Basic
• Hp Alm
• Crystal Reports 10.0