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Senior Validation Specialist (Boston)
Senior Validation Specialist (Boston)Compliance Group Inc • Boston, MA, United States
Senior Validation Specialist (Boston)

Senior Validation Specialist (Boston)

Compliance Group Inc • Boston, MA, United States
15 hours ago
Job type
  • Full-time
Job description

Job Title : Sr. Quality Engineer CSA (VMS Site)

Duration : 24 Months

Work Arrangement : Hybrid (3 days per week onsite in Boston)

Hours / Week : 40

Managers Note :

Seeking a candidate with strong GMP and Laboratory Quality experience.

Position Overview :

The Sr. Quality Engineer will support the Quality Information team, collaborating with cross-functional business, operations, and QA groups to ensure compliance and quality oversight of computerized systems across GMP and GxP-regulated environments. The role is responsible for leading and performing quality activities related to system validation, change control, regulatory assessments, and lifecycle management, with a primary focus on applying Computer Software Assurance (CSA) principles to ensure risk-based, compliant validation of laboratory and manufacturing quality systems.

Key Responsibilities :

  • Provide quality oversight for enterprise-level computerized systems such as ServiceNow , QMS , ERP , Veeva EDC , Compass , RIM , Data Analytics , Lab , and Manufacturing Systems .
  • Apply CSA and GAMP 5 principles to drive efficient, risk-based system validation and ensure compliance.
  • Serve as Quality Owner for projects involving new implementations, upgrades, releases, periodic reviews, and CAPA / deviation management .
  • Review and approve project deliverables including validation plans, test scripts, execution results, reports, and traceability matrices.
  • Lead quality discussions, issue resolution, and ensure adherence to GMP and laboratory compliance standards .
  • Demonstrate strong understanding of Lab Quality Systems, Data Integrity , and regulatory expectations.
  • Communicate effectively with cross-functional teams to ensure systems align with business and compliance needs.
  • Identify quality risks, propose mitigation strategies, and support continuous improvement initiatives.
  • Ensure comprehensive quality assurance throughout system development, implementation, and maintenance phases.

Minimum Qualifications :

  • Bachelors degree in Computer Science, Information Technology , or a related field.
  • 8+ years of experience working with computerized systems in GMP-regulated environments.
  • Proven expertise in CSA / CSV activities across Enterprise and Lab systems.
  • Strong background in Lab Quality, GxP compliance , and risk-based validation.
  • Familiarity with ITIL and GAMP 5 validation lifecycle principles.
  • Excellent analytical, documentation, and problem-solving abilities.
  • Skilled in creating audit-ready documentation , process records, and test evidence.
  • Strong communication skills with the ability to translate complex compliance data into actionable insights.
  • Preferred Qualifications :

  • In-depth understanding of computerized system structures and module design.
  • Demonstrated experience managing projects and user acceptance testing .
  • Ability to design innovative, compliant, and risk-based validation strategies under CSA and GMP frameworks.
  • Advanced proficiency in technical writing for regulated environments.
  • Experience with Agile validation methodologies .
  • Working knowledge of Veeva Vault QMS, ServiceNow, and Application Lifecycle Management (ALM) systems with e-signature functionality.
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    Validation Specialist • Boston, MA, United States

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