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ICON plc

Senior Validation Analyst, Veeva EDC

ICON plc

. Lead scientific operations tasks requiring technical depth, with a focus on quality and continuous improvement .

Posted 11/2/2026full-timeChennai • IndiaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in validation activities, regulatory compliance, and quality assurance within the healthcare and pharmaceutical sectors. Capable of leading cross-functional collaborations and providing training to junior analysts while ensuring adherence to best practices and standards.

Highest-signal resume keywords
Validation ActivitiesRegulatory RequirementsAnalytical SkillsCommunication SkillsCollaboration

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Validation PlansProtocolsRisk AssessmentsImpact AnalysesDocumentationQuality ImprovementAttention to Detail
Soft Skills
Problem-SolvingEffective Communication
Industry Keywords
GxPFDAEMAHealthcarePharmaceuticalClinical Research

About the role

Key responsibilities & impact
  • Lead scientific operations tasks requiring technical depth, with a focus on quality and continuous improvement
  • Develop and execute validation plans, protocols, and reports for software, systems, and processes
  • Collaborate with IT, QA, and operational teams to assess validation needs and establish best practices
  • Conduct risk assessments and impact analyses to identify potential issues and recommend validation strategies
  • Document validation activities and maintain accurate records for audits and inspections
  • Provide training and guidance to junior analysts
  • Ensure systems and processes comply with regulatory standards and internal quality requirements

Requirements

What you’ll need
  • Bachelor's degree in Life Sciences, Engineering, Computer Science, or a related field
  • Extensive experience in validation activities within the healthcare, pharmaceutical, or clinical research sectors
  • Strong knowledge of regulatory requirements (e.g., GxP, FDA, EMA) and validation best practices
  • Excellent analytical and problem-solving skills, with a keen attention to detail and accuracy
  • Effective communication skills, with the ability to collaborate with cross-functional teams and convey complex information clearly
  • Willingness to travel as required (approximately 5%)
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways