Srinath Bharade

Associate Consultant

Hyderabad, Telangana, India6 yrs 9 mos experience
Most Likely To SwitchHighly Stable

Key Highlights

  • Over 3 years of experience in regulatory affairs.
  • Expertise in Veeva Vault and regulatory submissions.
  • Strong project management and communication skills.
Stackforce AI infers this person is a Regulatory Affairs Specialist in the Healthcare industry.

Contact

LinkedIn

Skills

Core Skills

Regulatory AffairsProject Management

Other Skills

Common Technical Document (CTD)CommunicationData ManagementData MigrationData VisualizationDatabase AdministrationDocumentationElectronic Common Technical Document (eCTD)Maintaining Professional RelationshipsManagementMicrosoft ExcelMicrosoft PowerPointMicrosoft WordMultitaskingOPAL

About

Professional regulatory associate with 40 months experience in regulatory CMC submissions, VEEVA VAULT System, RIMS, SAP & QMS - CAPA's. I am currently working at Medtronic's in Shared services team as Associate Regulatory affairs specialist.

Experience

Medtronic

Associate regulatory affairs system specialist

Aug 2021 – Present · 4 yrs 7 mos · Gurugram, Haryana, India

Veeva VaultRegulatory CMC submissionsProject ManagementRegulatory Affairs

Frey

Regulatory Affairs Associate

Jun 2019 – Aug 2021 · 2 yrs 2 mos · Hyderabad, Telangana, India

Education

Osmania University

Master's degree — Pharmaceutical Sciences

Jan 2017 – Jan 2019

Jawaharlal Nehru Technological University

Bachelor of Pharmacy - BPharm — Pharmaceutical Sciences

Jan 2013 – Jan 2017

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