Senior/Lead Technical Project Manager – Global LIMS

Novo Nordisk

Senior/Lead Technical Project Manager overseeing LabVantage LIMS delivery in a regulated environment at Novo Nordisk. Leading quality and integration efforts across laboratory operations worldwide.

Posted 7/9/2026full-timeBangalore • 🇮🇳 IndiaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in LIMS implementation and upgrades, ensuring compliance with regulatory standards and alignment with laboratory operations. Proficient in stakeholder management and communication, driving effective project delivery in a regulated Life Sciences environment.

Highest-signal resume keywords

LIMS ImplementationComputer Systems Validation (CSV)GxP ComplianceStakeholder ManagementRESTful API Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Software DevelopmentLIMS DevelopmentSystem IntegrationAutomation Test ManagementRisk AssessmentTechnical Documentation ReviewChange ControlData IntegrityMiddleware PlatformsValidation Protocols

Soft Skills

Verbal CommunicationWritten CommunicationInterpersonal SkillsDecision-MakingCoordination Abilities

Tools & Technologies

LabVantage LIMSMuleSoftSOAP ServicesQuality Management System (QMS)AI Technologies

Industry Keywords

Life SciencesPharmaceutical IndustryGAMP 521 CFR Part 11Regulatory Inspections

Tech Stack

Tools & technologies

SOAP

About the role

Key responsibilities & impact

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, while upholding data integrity processes by proactively identifying and escalating risks
Supporting internal audits and regulatory inspections with summarised validation data and coordinated regulatory responses

Requirements

What you’ll need

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.

Benefits

Comp & perks

Opportunities to learn and develop
Unique culture