Technical Lead
Ireland
Job Description
Technical Lead
Others, Munster

Job Summary

Computerized System Validation (CSV)

Job Roles/Responsibilities: 

  • Act as Validation and Qualification Lead on a large laboratory remediation projects, with specific focus on Laboratory Standalone COTS systems
  • Author the typical validation, qualification, and testing documentation such as Validation Plans/Summaries, Test Plans/Summaries, User Requirements, Configuration Specifications, Trace Matrix, Qualification Protocols (IQ/OQ/PQ) and Scripts, Testing Defects, etc.
  • Assist systems users with defining, authoring and documenting system use in user, admin, and maintenance SOPs
  • Coordinate alignment of systems users from various company groups on validation and qualification documentation
  • Proactively communicate with various company organizations and systems vendors to ensure the project hurdles are overcome quickly and effectively
  • Provide tactical guidance and coaching in support of systems testing efforts with the stakeholders
  • Act as validation task lead: take ownership of related tasks, work under minimal supervision, utilize the industry experience and best judgment to make tactical decisions, stay proactive, etc.
  • Support the review & approval of key quality deliverables including SDLC, Change control, Deviations, CAPAs.  Etc. 
    Attend periodic review meetings, cutover migration, hyper care support, any enhancements planning, design and/or implementation meetings as required.
  • Good at customer handling and liaising with all stakeholders. 

 

Qualifications & Education:

  • 5+ years of Lab Systems validation experience is required. 
  • Specific hands-on experience with validating, qualifying, and/or using Pharmaceutical QC Lab Standalone COTS systems are required, including the authoring end to end of life cycle documents (including systems use and administration procedures)
  • Understanding of Data Integrity concepts is required
  • Excellent communication and written skills required
  • You have strong analytical skills and an aptitude for decision-making
  • You show resilience when faced with challenges
  • You believe in continuous learning and growth

Key Responsibilities

Computerized System Validation (CSV)

Job Roles/Responsibilities: 

  • Act as Validation and Qualification Lead on a large laboratory remediation projects, with specific focus on Laboratory Standalone COTS systems
  • Author the typical validation, qualification, and testing documentation such as Validation Plans/Summaries, Test Plans/Summaries, User Requirements, Configuration Specifications, Trace Matrix, Qualification Protocols (IQ/OQ/PQ) and Scripts, Testing Defects, etc.
  • Assist systems users with defining, authoring and documenting system use in user, admin, and maintenance SOPs
  • Coordinate alignment of systems users from various company groups on validation and qualification documentation
  • Proactively communicate with various company organizations and systems vendors to ensure the project hurdles are overcome quickly and effectively
  • Provide tactical guidance and coaching in support of systems testing efforts with the stakeholders
  • Act as validation task lead: take ownership of related tasks, work under minimal supervision, utilize the industry experience and best judgment to make tactical decisions, stay proactive, etc.
  • Support the review & approval of key quality deliverables including SDLC, Change control, Deviations, CAPAs.  Etc. 
    Attend periodic review meetings, cutover migration, hyper care support, any enhancements planning, design and/or implementation meetings as required.
  • Good at customer handling and liaising with all stakeholders. 

 

Qualifications & Education:

  • 5+ years of Lab Systems validation experience is required. 
  • Specific hands-on experience with validating, qualifying, and/or using Pharmaceutical QC Lab Standalone COTS systems are required, including the authoring end to end of life cycle documents (including systems use and administration procedures)
  • Understanding of Data Integrity concepts is required
  • Excellent communication and written skills required
  • You have strong analytical skills and an aptitude for decision-making
  • You show resilience when faced with challenges
  • You believe in continuous learning and growth

Skill Requirements

Other Requirements

Information at a Glance

Why HCLTech?

At HCLTech, you'll supercharge your potential. You'll find your career. And you'll find your spark. All at a place that knows that helping its customers stay on top starts by putting its people first.

HCLTech is a global technology company, home to more than 223,000 people across 60 countries, delivering industry-leading capabilities centered around digital, engineering, cloud and AI, powered by a broad portfolio of technology services and products. We work with clients across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, Technology and Services, Telecom and Media, Retail and CPG, and Public Services. Consolidated revenues as of 12 months ending June 2026 totaled $14.8 billion.