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GSK

Develops medicines, vaccines, and consumer health

Lead Analyst - Design Assurance & Product Management, Operations

Security Governance, Risk & CompliancePosted on Nov 9
Full-timeBengaluru, Karnataka, IndiaNo salary listedHybrid

About the Job

Requirements

  • 10+ years of experience in cybersecurity, technology governance, or programme coordination, with a focus on Design Assurance Operations.
  • Experience running Design Assurance intake and triage, including scope and specification checks, allocating requests to the correct domain analyst, and managing the review calendar.
  • Experience owning Design Assurance tooling and templates, including GRC systems, SharePoint, review packs, and automated intake, reminders, and reporting.
  • Experience administering a Design Assurance Committee, including agendas, minutes, and actions, and maintaining the Design Assurance knowledge base and requestor onboarding.
  • Experience using AI and automation to streamline Design Assurance intake, triage, and reporting, and routing AI tool reviews to the appropriate specialist.

Responsibilities

  • Run Design Assurance intake in ServiceNow by logging and scope-checking review requests and routing them to the appropriate domain reviewer across Network and Zero Trust, Platform Security and MDR, Application Security, Data Security and Cloud, OT Security and Vulnerability and Configuration Management, and Cryptography, PQC and AI Security.
  • Confirm that the architecture specification exists and is current before a review starts, and reject requests that arrive without one.
  • Maintain the review calendar and reviewer allocation against capacity, and publish turnaround commitments to requesting programmes.
  • Administer and version-control Design Assurance templates and tooling, publish approved updates, and withdraw superseded versions.
  • Produce practice reporting in Power BI covering throughput, first-time-pass rate, turnaround against SLA, domain coverage, and bypass rate.
  • Prepare governance forum packs and supporting evidence trails to GxP record-keeping standards.
  • Track findings and time-bound conditions to closure, follow up on stalled items, and escalate aged items by name.
  • Maintain the assurance register as the record of what was reviewed, by whom, and with what outcome, so coverage can be evidenced for internal audit and regulatory inspection.
  • Assemble audit and regulatory evidence requests, including the decision trail demonstrating that a review operated.
  • Improve the intake and coordination process and automate manual steps.
  • Use approved AI tools to improve individual and team productivity, validate outputs, and follow GSK Responsible AI, privacy, and security requirements.

Desired Qualifications

  • Experience with GRC tooling such as ServiceNow and SharePoint or equivalent repository management.
  • Experience with Power BI or equivalent tools for Design Assurance performance and governance reporting.
  • Experience with workflow automation or low-code tooling for intake and reminders.
  • Exposure to security architecture and GxP-compliant documentation practices.
  • Experience operating a controlled records environment with retention, version history, and approval trails that can withstand inspection without reconstruction.
  • A Bachelor's degree in a relevant discipline, or equivalent professional experience.

About the Company

GSK

Develops medicines, vaccines, and consumer health

GSK is a global healthcare company focused on three main areas: Pharmaceuticals, Vaccines, and Consumer Healthcare. It develops medicines, vaccines, and consumer health products to improve health outcomes worldwide. Its products address diseases in respiratory, HIV, oncology, and immuno-inflammatory areas; vaccines for influenza, shingles, and COVID-19; and over-the-counter wellness products. The company relies on substantial R&D and strategic partnerships to bring new products to market and to address health needs. Revenues come from sales of medicines, vaccines, and consumer health items, often complemented by patient support programs and collaborations with governments and biotech partners.

Company size
10,001+
Company stage
IPO
Headquarters
London, United Kingdom
Founded
1891

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