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Valspec
Documentation / Data Lead
Career Insights for Validation Specialist
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Based on North Carolina data
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What they do
A Validation Specialist tests and documents the validity and accuracy of manufacturing systems and equipment. Tests processes and manages process validations. Provides technical support and implements operating procedures. May create documentation to show that a manufacturing or production process has consistent results and meets quality standards.
$88,298 / year median in North Carolina
+6% projected growth
Job Description
Documentation / Data Lead Valspec - 4.6 Raleigh, NC Job Details 5 hours ago Benefits Health insurance Tuition reimbursement 401(k) matching Employee stock ownership plan Qualifications Project reporting Data integrity assurance Performance dashboards Monitoring compliance data Resource planning methods Document control experience within manufacturing industry Metrics Reporting Data quality management Quality compliance management Data reporting support Senior level Process management Pharmaceutical manufacturing facility experience Full Job Description Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals. Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies. Documentation/Data Lead — East Coast (Greenfield Pharma/Biotech Program) About the Role Join a major greenfield pharmaceutical manufacturing program as Documentation/Data Lead, owning CQV documentation governance and data management across the project lifecycle. What You'll Do Manage document lifecycle processes Oversee turnover packages and readiness documentation Drive data integrity and reporting standards Support metrics, dashboards, and compliance tracking What We're Looking For Strong CSV management and deliverable governance experience Background in document review, resource planning, and quality systems oversight Experience on large capital pharma/biotech or advanced manufacturing projects