CSV / Validation Specialist BMS

Prev CSV / Validation Specialist - BMS#26-06364 Lebanon, IN All On-site Job Description Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting services. We are in search of a highly motivated candidate to join our talented Team.

Job Title:

CSV / Validation Specialist - BMS

Location:

Lebanon, Indiana

Duration:

Contract

Role Summary:

Domain (Industry): Life Sciences & Pharma

Total Experience:

7-10 years Lead validation lifecycle activities for automation and control systems at LMF, including DeltaV, PI Historian, Rockwell PLC/HMI, and Metasys platforms. Develop and execute validation plans (VP), user requirement specifications (URS), functional specifications (FS), design specifications (DS), and configuration specifications (CS) for automation systems. Author and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Generate and maintain requirements traceability matrices (RTMs) linking requirements through design, testing, and acceptance. Author validation summary reports (VSR) documenting validation oues, deviations, and acceptance rationale. Perform 21 CFR Part 11 gap assessments for electronic records, electronic signatures, and audit trailpliance across all in-scope automation systems. Conduct risk assessments (including GAMP 5 categorization and functional risk assessments) for automation and control systemponents. Manage validation change control by assessing the impact of system changes, patches, and upgrades on the validated state and determining revalidation requirements. Support periodic review activities to confirm that automation systems remain in a validated state and that validation documentation is current. Define and execute the CSV/validation scope for the ServiceNow platform in collaboration with the ServiceNow Process Owner. Validate system integrations between automation platforms and ServiceNow, including event connectors, CMDB connectors, API interfaces, and access provisioning workflows. Draft and maintain standard operating procedures (SOPs) related toputer systems validation for automation systems. Support audit readiness by ensuring validation documentation is inspection-ready and aligned with FDA, EMA, and Lilly corporate quality standards. Provide support for data integrity assessments across automation and historian systems. Assist withmissioning and qualification (C&Q) activities for new automation equipment. Support remediation of validation findings from internal audits or regulatory inspections. Advise on validation strategy for future automation system upgrades and expansions.

Relevant Experience:

7-10 years Mandatory skills: Demonstrated experience inputer systems validation (CSV) for automation and control systems in a pharmaceutical/GMP-regulated environment. Strong knowledge of GAMP 5 methodology, V-model lifecycle, and risk-based validation approaches. Experience with 21 CFR Part 11pliance, including assessment of electronic records, electronic signatures, and audit trail requirements. Proficiency in developing validation deliverables across SDLC Life cycle. Experience with DCS, PLC/HMI, and/or historian systems in a manufacturing environment. Strong understanding of FDA and EMA regulatory expectations forputerized system validation. Desired skills: Direct experience validating DeltaV, PI Historian, Rockwell FactoryTalk, or Metasys platforms. Experience with ServiceNow platform validation or ITSM system validation in a GxP context. Familiarity with data integrity principles (ALCOA) and data governance frameworks. Experience with Kneat, ValGenesis, or similar electronic validation management systems. Ampcus is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, national origin, age, protected veterans or individuals with disabilities.