CSV Lead

Katalyst CRO; Tulsa (OK); On-site; USD 120,000 - 160,000; Full time

Job summary

Katalyst CRO in Tulsa, OK is seeking an experienced CSV Lead to oversee validation activities for GxP computer systems. The role requires extensive CSV lifecycle management, strong FDA and global regulatory compliance, and the ability to develop validation documentation, risk assessments, and validation plans that meet business needs.

You will coordinate with IT, Quality Assurance, Engineering, and Manufacturing; mentor junior CSV engineers; and support internal and regulatory audits and

Qualifications

• 8–12+ years of CSV experience in pharma or life sciences.
• Strong knowledge of 21 CFR Part 11 and Annex 11.
• Experience with IQ/OQ/PQ validation activities.
• Ability to mentor junior CSV engineers.

Responsibilities

• Lead end-to-end CSV activities for GxP systems.
• Develop and review validation plans, protocols, and reports.
• Ensure compliance with global regulatory requirements.
• Coordinate with IT, QA, and Manufacturing teams.
• Support internal audits, customer audits, and regulatory inspections.
• Mentor junior CSV engineers and maintain lifecycle documentation.

Skills

CSV lifecycle management

FDA compliance

GxP validation

Cross-functional leadership

Education

Bachelor's or Master's degree in a related field

Tools

LIMS

MES

ERP (SAP)

SCADA

DMS

QMS

EBR

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.

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).