IT Application Architect, Laboratory Information Management System, LIMS

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Pune, Mahārāshtra, IND
In-Office
Senior level
Healthtech • Pharmaceutical
The Role
The IT Application Architect will design and implement technical solutions for LIMS, manage technical delivery and platform roadmaps, and support compliance in a regulated environment.
Summary Generated by Built In

Edwards Lifesciences is expanding its global technology capabilities with the launch of a new IT Innovation Hub in Pune, India. The Hub strengthens the technology foundation that supports our business worldwide, working in close partnership with teams across regions to deliver reliable, high-quality solutions at scale. Designed as a long-term investment, the Pune Hub will advance newer digital capabilities such as automation, data, AI, and cloud, and will include roles spanning end user services, application development, and enterprise platform teams. Together, these teams will help Edwards operate more efficiently and accelerate innovation in support of our mission of advancing patient care.

The IT Application Architect, LIMS, will serve as the technical owner of our enterprise Laboratory Information Management System (LIMS) reporting to the Director, IT Business Partner of Global Quality and Lab Technologies. As the IT Application Architect, LIMS, you will be a key member of a global quality technical transformation team implementing and guiding the technical evolution and optimization of LIMS across a global organization. 

How you’ll make an impact:

  • Design and implement LIMS technical solutions to meet business requirements. 
  • Oversee all technical delivery for LIMS and assume technical ownership of the system. 
  • Define and implement IT LIMS standards, ensuring alignment with global IT and industry best practices for software development and system implementation.
  • Manage the technical platform roadmap, including regular platform updates and prompt resolution of IT security vulnerabilities within established SLAs.
  • Advocate for remediation of technical debt and continuous system improvements to drive business growth and development.
  • Partner with business leaders to understand organizational needs and assess implementation complexity for both in-house and project-funded initiatives.
  • Act as a steward for LIMS integrity, making informed recommendations to minimize unnecessary customization and preserve system purpose.
  • Execute a shift-left strategy for support and maintenance, transferring Level 2 (L2) support to the global team while retaining Level 3 (L3) support, problem management, and change management within the transformation team.

What you’ll need (Required):

  • Bachelor’s degree with 8+ years of hands-on experience designing, configuring, implementing, and maintaining enterprise LabWare and/or LabVantage LIMS.
  • Experience working with 21 CFR part 11.
  • Experience working in a regulated environment, and strong understanding of GxP concepts and regulatory compliance in a pharmaceutical/medical device setting.
  • Experience with commercial off the shelf applications and a solid understanding of the importance master data structure plays in a scalable enterprise solution.
  • Experience writing and executing validation deliverables (e.g., IQ/OQ/SDD) in the software development life cycle (SDLC) for validated, regulated, applications.

What else we look for (Preferred):

  • Strong background in server-client and/or web hosted application architecture, integrations to applications and equipment; preference for experience with laboratory instruments and enterprise systems (such as ERP and MES).
  • Experience with server administration required to support an enterprise application.
  • Experience with structured query language (SQL) and relational databases.
  • Experience / knowledge with remote desktop and other web hosting platforms.
  • Experience working with application vendors, and 3rd party consulting companies on technology implementations and delivery.
  • Experience working in a global, highly matrixed, and team-oriented IT environment.
  • High energy, self-motivation, and results-driven mindset with an excitement to learn new technologies.
  • Have a passion for our mission at Edwards Lifesciences.
  • Comfortable communicating and presenting ideas/recommendations to a senior leadership level.

If you are passionate about advancing laboratory information management, thrive in collaborative global teams, and want to make a significant impact on business and IT transformation, we invite you to apply.

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Skills Required

  • Bachelor's degree with 8+ years of hands-on experience designing, configuring, implementing, and maintaining enterprise LabWare and/or LabVantage LIMS
  • Experience working with 21 CFR part 11
  • Experience working in a regulated environment, and strong understanding of GxP concepts
  • Experience writing and executing validation deliverables (e.g., IQ/OQ/SDD) in the software development life cycle for validated applications

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Retirement Support Retirement programs include a 401(k) match complemented by a separate profit‑sharing contribution. These elements add meaningful long‑term value to total compensation.
  • Equity Value & Accessibility An employee stock purchase plan with a discount and look‑back feature, alongside stock awards for eligible roles, provides notable upside. Program expansions indicate continued accessibility.
  • Leave & Time Off Breadth Time‑off policies include generous PTO, company holidays, and a year‑end holiday shutdown. These offerings enhance work‑life support when available at the site.

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The Company
Draper, Utah
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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