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GSK

Develops medicines, vaccines, and consumer health

Principal – LabWare LIMS

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listed

About the Job

Requirements

  • A bachelor's or master's degree in engineering, Computer Science, Information Technology, Life Sciences, or a relevant technical discipline, or equivalent practical experience.
  • At least 7 years of hands-on technical experience with LabWare LES and preferably LabWare LIMS version 8, including configuration and scripting.
  • A proven track record delivering and supporting QC laboratory systems in a GxP-regulated environment.
  • Experience designing and configuring LES workflows.
  • Experience integrating instruments and systems such as LIMS, ERP, and middleware.
  • Experience with incident, problem, and change management processes.
  • Hands-on experience with calculations and parsing queries to handle BAU requests.
  • A good understanding of QC laboratory processes and terminology.
  • Experience with global or multi-site QC system deployments.
  • Hands-on experience applying automation, DevOps, and AI.
  • Knowledge of Computer System Validation, 21 CFR Part 11, Annex 11, and data integrity principles.
  • Familiarity with ITIL or similar service management frameworks.
  • Experience working with external vendors and offshore teams.

Responsibilities

  • Lead the design, configuration, and implementation of LabWare LES solutions for QC laboratories.
  • Translate QC laboratory processes and methods into robust LES workflows and electronic work instructions.
  • Define and maintain LES standards, templates, and best practices across projects and sites.
  • Own technical quality for the assigned scope, including specifications, design documentation, configuration records, and technical validation evidence.
  • Drive engineering lessons learned and cross-team continuous improvement.
  • Provide technical oversight and guidance to Technical Engineers and vendors on LES configurations.
  • Lead the design and implementation of new LES functionality and review Technical Engineers’ configurations.
  • Lead integration activities with LIMS, instruments, and other QC systems.
  • Participate in requirements gathering, configuration, unit testing, and user acceptance testing.
  • Use LES automation capabilities, including custom calculations, processing workflows, scheduling, and scripts or macros where applicable, to streamline QC operations.
  • Identify opportunities to automate repetitive tasks and standardise workflows.
  • Contribute to the design and execution of LES Citrix-to-Azure migration, including environment build, cutover planning, testing, and rollout.
  • Use AI-assisted development, agent-based workflows, and prompt templates for engineering, testing, documentation, and support.
  • Act as the technical subject-matter expert for BAU requests, including static data changes, incidents, and problems related to LabWare LES.
  • Troubleshoot complex issues, perform root cause analysis, and drive permanent fixes.
  • Deliver small changes and corrective enhancements following change management processes.
  • Monitor system performance, stability, and data integrity, and propose continuous improvements.
  • Ensure LES solutions comply with GxP, data integrity (ALCOA+), and regulatory expectations.
  • Support Computer System Validation activities, including risk assessments and test evidence.
  • Maintain current technical and support documentation for LES configurations and changes.
  • Work closely with QC and site users, business analysts, validation teams, and infrastructure teams.
  • Share knowledge within the team and contribute to continuous improvement of LES support processes.
  • Adhere to agreed service-level agreements, priorities, and service management practices.

Desired Qualifications

  • Strong analytical and structured problem-solving skills.
  • Ability to translate architecture and product direction into clear technical designs and implementation activities.
  • Clear technical writing and disciplined maintenance of specifications, designs, test evidence, and configuration records.
  • Understanding of interfaces, workflows, data, environments, monitoring, and operational support.
  • Awareness of security, quality, validation, data integrity, resilience, and change controls.
  • Ability to collaborate across global business, site, engineering, architecture, product, service, and supplier teams.
  • A continuous-improvement mindset emphasizing standardisation, reuse, automation, and knowledge sharing.
  • Technical leadership and the ability to challenge designs constructively.
  • Coaching and knowledge-transfer capability.
  • Confidence communicating technical risk and recommendations to governance and senior stakeholders.

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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