CSV Lead

Creative Solutions Services, LLC; Springfield (IL); On-site; USD 120,000 - 180,000; Full time

Job summary

Creative Solutions Services, LLC seeks an experienced Computer System Validation (CSV) Lead to oversee validation activities for GxP computerized systems. You will manage IQ/OQ/PQ, risk assessments, and regulatory alignment across IT, QA, and manufacturing teams.

The role requires 8–12+ years in CSV within pharma or life sciences, with strong GMP and FDA/EMA knowledge. You will mentor junior engineers and maintain lifecycle documentation per SOPs.

Qualifications

• 8–12+ years of CSV experience in pharma or life sciences
• Strong knowledge of GxP regulations and CSV lifecycle
• Experience validating enterprise systems (LIMS, MES, SAP, etc.)

Responsibilities

• Lead end-to-end CSV activities for GxP computerized systems.
• Develop and review Validation Plans, Protocols, Risk Assessments, Traceability Matrices, and Validation Summary Reports.
• Execute IQ, OQ, and PQ activities.
• Ensure compliance with 21 CFR Part 11, Annex 11, GAMP 5, FDA and EMA requirements.
• Review URS, FS, and DS documents.
• Perform risk assessments using GAMP 5 methodology.
• Manage deviations, CAPAs, change controls, and periodic reviews.
• Support software implementation, upgrades, migrations, and decommissioning.
• Coordinate validation activities with IT, QA, Engineering, Manufacturing, and Business teams.
• Support internal and regulatory audits and inspections.
• Mentor junior CSV engineers and provide guidance.
• Maintain validation lifecycle documentation per SOPs.

Education

Bachelors or Masters in CS/IT/Bio/Pharma/Engineering

Tools

LIMS

MES

ERP SAP

QMS

DMS

SCADA

PLC/HMI

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.

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).