Medical Devices (CSV

Trusting your profile quality, we accept Only 2 Relevant profiles from each of our partner, ensure budget is not exceeded. Unless TAG SPOC look for additional profiles, please don’t Supply additional Profiles. Note: Profiles without tracker will not be consider for evaluation. Candidates details can shared to TAG SPOC directly with the details filled in below tracker format; mandatorily me in CC. If You need any further clarification on JD, please reach TAG SPOC before supplying profile itself. Max Margin can be 18% Only . Margin will be on Markup Model Only, please don’t supply Profile if you cannot disclose CTC & Margin to us. TAT for this Supply Valid for 24 hrs Only. Please do not Supply any beyond the timeline. Any Profiles, which does not get submit thru TAG and VMT, Credits, will not be given to respective partner. Any Non-Adherence to the above shall lead us to stop supplying any further requisitions to you. Please find the Detailed JD & SPOC details below. TAG SPOC: Dilip Gomathinayagam P dilip_gomat@hcltech.com S.No Date Vendor CV ID Customer Skill Name Phone No E-mail Id Qualification with Stream Total Exp Rel Exp Relevant skill Relevant skill exp Current Company Deployed Company CTC E.CTC Current Location Preferred Location N.P Vendor Margin Final Bill Rate Approved TP SR DBS/DBS/2026/2817525 BR 1647522BR Total Open Positions 20 Band E2.1 & E2.2 Experience 4 – 10 Yrs Skill CSV in Medical Devices related IT system and Experience in handling quality management in Merger and Acquisition Bill Rate 230000 SOW signed Yes / No No Billing Start Date 2nd March Customer J&J Customer BGV Yes / No Yes Tentative Project Timeline 6 Months Work Location Pan India Detailed JD Experience in validating Medical Devices related IT system and Merger and Acquisition 3+ years’ experience with System Development Lifecyle 7+ years’ experience in Computer System Validation (Based on the role selected) Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs. Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures. Preferred tools knowledge and experience: JIRA, ServiceNow, XRAY and Change Record review Experience in Acquisition, Separation and Divestiture Experience in Infrastructure Qualification Should be experienced in Test scripts, executions, and defect reviews. Strong verbal and written communication skills. Ability to work as a team player, lead a team or accomplish tasks without supervision. Ability to work with remote teams and support several changes/projects simultaneously. Ability to provide Validation guidance, timely reviews, and escalations to TQ management.