Job Description

Department- LAPS Development

Company- Novo Nordisk Global Business Services (GBS)

Lead the end-to-end delivery of a mission-critical laboratory platform that touches every corner of our global QC and R&ED operations – and ultimately, the patients who depend on our medicines.

Your new role

As a Senior/Lead Technical Project Manager for globalLIMS, you will lead hands-on delivery of LabVantage LIMS programs in a GxP-regulated environment – covering integrations, releases, upgrades, change coordination and validation readiness. You will also champion IT DevOps automation and emerging AI capabilities to accelerate releases, improve quality and strengthen operational stability across environments.

Day-to-day your responsibilities will include:

• Owning end-to-end delivery of LIMS implementation and upgrade programs, ensuring alignment with laboratory operations, business goals and regulatory requirements
• Creating and maintaining comprehensive execution plans aligned with project timelines, budgets and our Quality Management System (QMS)
• Acting as the voice of Quality in cross-functional teams, driving CSV strategy and standards across all project phases
• Reviewing and approving technical documentation, risk assessments, CSV protocols, test scripts and deviations in line with Novo Nordisk quality standards
• Leading requirement analysis, design and development discussions with Line of Business and end users to deliver feasible, compliant solutions
• Supporting the globalLIMS AM team on critical incidents, root cause analysis and deployment activities for planned and unplanned releases
• Adopting AI and automation technologies to enable faster releases, and upholding data integrity processes by proactively identifying and escalating risks
• Supporting internal audits and regulatory inspections with summarised validation data and coordinated regulatory responses

Your new department

In Enterprise IT & Quality, you will be part of a business area that drives impact across the full Novo Nordisk value chain. We strive to stay close to our stakeholders in the business to ensure we deliver on their needs, helping reach millions of people living with serious chronic diseases. Our focus is on being at the forefront within our three areas; ensuring the highest quality for patients, being a trusted tech leader and an environmentally responsible business.

You will join LIMS, Planning & Ecosystems, based in our Global Business Services (GBS) hub in India. The team is responsible for the development, operation, maintenance and support of QC lab systems, with globalLIMS as our flagship platform used across QC and R&ED worldwide. Working closely with stakeholders at HQ and across regions, you will operate in a truly global environment where cultural awareness, collaboration and technical excellence come together.

Your skills & qualifications

We are looking for an experienced technical leader who combines deep LabVantage LIMS expertise with a strong quality mindset and the ability to influence stakeholders across geographies. To succeed in this role, you will bring:

• A Bachelor's degree in Computer Science, Information Technology or a related field
• 12+ years of professional experience in software development, including a minimum of 6+ years as a Technical Project Manager working with LabVantage LIMS (v8.5 or higher) in a regulated Life Sciences environment
• Significant experience in the pharmaceutical industry with a focus on Computer Systems Validation (CSV); deep experience with LIMS or MES implementation is highly preferred
• Strong knowledge of GxP, GAMP 5 and 21 CFR Part 11, with familiarity in automation test management tools and data integrity, change control and validation expectations
• Extensive experience in LIMS development and system integrations using RESTful APIs, SOAP services and middleware platforms (e.g. MuleSoft) for scalable, secure and compliant integrations with enterprise applications
• Proven stakeholder management skills, working across laboratory users, Quality, IT, vendors and integration partners – with the ability to translate business needs into effective technical solutions
• Excellent verbal and written communication skills in English, coupled with strong interpersonal, decision-making and coordination abilities across diverse cultures and time zones

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

Deadline- 23 June 2026

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.