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Merck

Makes medicines, vaccines and animal treatments

Business System Validation Senior Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWarsaw, PolandNo salary listed

About the Job

Requirements

  • A non-degree candidate must have at least 8 years of relevant experience in system validation or a testing lead role.
  • An associate's degree candidate must have at least 7 years of relevant experience in system validation or a testing lead role.
  • A bachelor's degree candidate must have at least 5 years of relevant experience in system validation or a testing lead role.
  • A master's or doctoral degree candidate must have at least 2 years of relevant experience in system validation or a testing lead role.
  • Have deep understanding of compliance and documentation standards, including GxP, 21 CFR Part 11, and audit traceability practices.
  • Have deep knowledge of validation lifecycle management, risk-based testing, and regulatory compliance frameworks.
  • Be proficient in enterprise test management tools and automation platforms.
  • Have experience implementing AI-augmented validation frameworks and model governance practices.
  • Prioritize independently and escalate issues with context, impact, and recommendations.
  • Translate technical topics for non-technical stakeholders and build alignment on trade-offs.
  • Manage difficult conversations constructively and negotiate timeline and quality expectations.
  • Deliver clear status updates, decisions, and blockers, and maintain decision logs.
  • Identify and understand problems and opportunities by gathering, analyzing, and interpreting quantitative and qualitative information; solve complex problems and apply knowledge of business challenges; and weigh multiple options and implications.
  • Communicate effectively, promote teamwork and open discussion, engage and motivate teammates, and inspire performance aligned with the organization's purpose and strategic framework.
  • Build self-insight, recognize personal strengths, development needs, and impact on others, adapt behavior accordingly, and serve as a resource, coach, and guide for colleagues.

Responsibilities

  • Lead end-to-end execution of complex system validation activities with end users across multiple system releases, aligned with program-level requirements, platform standards, and regulatory expectations.
  • Develop validation strategies, risk assessments, coverage models, and test approaches for large-scale system implementations and cross-functional platform initiatives.
  • Support cross-functional system readiness planning by evaluating validation impacts of new features, integrations, platform releases, and automation workflows.
  • Oversee test execution for multiple systems or releases, manage issue resolution, escalate risks, and ensure timely delivery of validation milestones.
  • Ensure traceability across requirements, design specifications, test cases, and objective evidence throughout the validation lifecycle; identify gaps and drive remediation.
  • Lead root cause analysis and corrective/preventive action activities for complex testing issues; guide teams on risk mitigation and quality improvements.
  • Review, guide, and provide final approval for validation deliverables, including validation plans, test plans, test scripts, and test summaries.
  • Drive adherence to standard operating procedures and regulatory requirements, and contribute to authoring, updating, and harmonizing validation processes, templates, and standards.
  • Monitor and report validation key performance indicators across projects, identify systemic issues, and lead continuous improvement to enhance validation quality, efficiency, and audit and inspection readiness.
  • Serve as a validation subject matter expert during audits and inspections by preparing and presenting validation packages, responding to auditor questions, and ensuring complete, traceable documentation is available.
  • Mentor junior validation staff through training, technical guidance, and quality oversight to promote consistent validation best practices.
  • Lead day-to-day activities, drive issue triage to closure, and coordinate stakeholders.
  • Mentor junior analysts on tools, checks, documentation quality, and best practices.

About the Company

Merck

Makes medicines, vaccines and animal treatments

Merck develops prescription medicines, vaccines and veterinary treatments for patients, health systems and animal owners worldwide. Its vaccine portfolio includes Gardasil 9, which helps prevent cancers and other diseases caused by several types of human papillomavirus. The company takes potential treatments through laboratory research and clinical trials, then manufactures and sells approved products to drug distributors, hospitals, physicians and governments. Its animal health division sells medicines and vaccines to veterinarians, farmers and pet owners, while selected drug partnerships also earn shared profits or royalties. Founded in 1891, Merck is headquartered in Rahway, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Rahway, NJ
Founded
1891

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