CSV Lead

Fives DyAG Corp.; Tulsa (OK); On-site; USD 110,000 - 160,000; Full time

Job summary

Fives DyAG Corp. is seeking an experienced Computer System Validation (CSV) Lead to oversee validation activities for GxP computer systems and ensure compliance with FDA and global requirements.

You will drive IQ/OQ/PQ execution, author validation plans and reports, mentor junior engineers, and coordinate with IT, QA, and manufacturing to maintain robust validation lifecycle documentation.

Qualifications

• 8–12+ years of CSV experience in pharma or life sciences.
• Strong knowledge of GxP regulations and 21 CFR Part 11.
• Experience with IQ, OQ, PQ validation activities.
• Experience with regulatory inspections and audits.

Responsibilities

• Lead end-to-end CSV activities for GxP systems.
• Develop and review validation plans, protocols, and reports.
• Execute IQ/OQ/PQ testing and documentation.
• Coordinate with IT, QA, Engineering, and Manufacturing.
• Mentor junior CSV engineers.

Skills

CSV lifecycle management

Regulatory compliance

Risk assessments

Cross-functional collaboration

Documentation practices

Education

Bachelor's degree in Computer Science / IT / Biotech / Pharmacy / Engineering

Tools

LIMS

MES

ERP (SAP)

SCADA

PLC/HMI

QMS

DMS

Job description

Job Description:

We are seeking an experienced Computer System Validation (CSV) Lead to oversee validation activities for computerized systems used in regulated GxP environments. The ideal candidate will have extensive experience in CSV lifecycle management, FDA and global regulatory compliance, validation documentation, risk assessments, and cross-functional collaboration to ensure validated systems meet business and regulatory requirements.

Responsibilities:

• Lead end-to-end Computer System Validation (CSV) activities for GxP computerized systems.
• Develop and review Validation Plans, Validation Protocols, Risk Assessments, Traceability Matrices, and Validation Summary Reports.
• Execute and oversee IQ, OQ, and PQ activities.
• Ensure compliance with 21 CFR Part 11, Annex 11, GAMP 5, FDA, EMA, and other global regulatory requirements.
• Review User Requirements Specifications (URS), Functional Specifications (FS), and Design Specifications (DS).
• Perform risk assessments using GAMP 5 methodology.
• Manage deviations, CAPAs, change controls, and periodic reviews.
• Support software implementation, upgrades, migrations, and decommissioning projects.
• Coordinate validation activities with IT, Quality Assurance, Engineering, Manufacturing, and Business teams.
• Support internal audits, customer audits, and regulatory inspections.
• Mentor junior CSV engineers and provide technical guidance.
• Maintain validation lifecycle documentation according to company SOPs.

Requirements:

• Bachelor's or Master's degree in Computer Science, Information Technology, Biotechnology, Pharmacy, Engineering, Life Sciences, or a related field.
• 8–12+ years of Computer System Validation experience in the pharmaceutical, biotechnology, medical device, or life sciences industry.
• Strong understanding of GxP regulations and computerized system validation.
• Experience validating enterprise systems such as:
  • LIMS.
  • MES.
  • ERP (SAP).
  • Laboratory Systems.
  • SCADA.
  • PLC/HMI.
  • Manufacturing Execution Systems.
  • Electronic Batch Records (EBR).
  • Quality Management Systems (QMS).
  • Document Management Systems (DMS).