CSV Lead

Katalyst Talent Agency
Piscataway, NJ, United States
1 day ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
10 years minimum
Compensation
$35,360.0 - $42,120.0
Working hours
Regular working hours

Tech stack

Data Integrity Laboratory Information Management Systems SAP (Applications) System Testing Iq/oq/pq Enterprise Software Applications Test Scripts Computerised Systems Trackwise Hardware Asset Management Veeva GXP

Job description

  • Lead and manage Computer System Validation (CSV) activities across regulated Life Sciences projects.
  • Develop and review validation plans, protocols, test scripts, reports, and validation documentation.
  • Lead validation lifecycle activities including URS, FS/DS, IQ, OQ, PQ, UAT, and RTM.
  • Perform risk assessments and ensure systems are validated in compliance with GxP requirements.
  • Support validation of GxP computerized systems, laboratory systems, manufacturing systems, and enterprise applications.
  • Manage deviations, CAPA, change controls, and validation-related investigations.
  • Provide technical leadership and coordinate with QA, IT, Engineering, Manufacturing, and Business teams.
  • Ensure compliance with FDA regulations, 21 CFR Part 11, GAMP5, and data integrity requirements.
  • Support audits, inspections, and inspection-readiness activities.
  • Manage project timelines, deliverables, and validation documentation., Job Title: Stock/Logistics Engineer (Hardware Asset management Lead) Location: Piscataway, NJ (Onsite) Stock/Logistics Engineer Will form part of the asset inventory team ens…
  • 4 hours ago
  • Apply easily +

Requirements

  • 10+ years of experience in CSV / Computer System Validation within Pharma, Biotech, Medical Device, or Life Sciences.
  • Strong knowledge of GxP validation lifecycle and risk-based validation approaches.
  • Hands-on experience with URS, FS/DS, IQ/OQ/PQ, UAT, RTM, and validation reports.
  • Strong knowledge of 21 CFR Part 11, GAMP5, FDA, and data integrity requirements.
  • Experience with deviations, CAPA, change control, and risk assessments.
  • Strong technical documentation and project leadership skills.
  • Experience working with cross-functional teams in regulated environments
  • Experience with laboratory systems such as LIMS, CDS, ELN, or SDMS.
  • Experience with manufacturing systems, MES, ERP, or automation-related systems.
  • Experience with systems such as LabWare, Empower, TrackWise, Veeva, or SAP.
  • Experience with data integrity assessments and audit/inspection support.
  • Experience leading CSV teams and managing multiple validation projects.

Benefits & conditions

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