CSV Specialist

JobDiva, Inc.; Madison (WI); On-site; USD 75,000 - 110,000; Full time

Job summary

Creative Solutions Services, LLC is seeking a CSV Specialist to support validation efforts for GxP systems in the pharmaceutical, biotechnology, or medical device sectors. The role emphasizes ensuring systems meet regulatory and company standards throughout the lifecycle.

The ideal candidate holds a relevant Bachelor's degree and has 3+ years of CSV experience, with strong documentation and communication skills.

Qualifications

• Bachelor's degree in engineering, life sciences, pharmacy or related field.
• 3+ years of CSV experience in regulated environment.
• Knowledge of GAMP 5, FDA 21 CFR Part 11, GMP, and Data Integrity (ALCOA+) principles.
• Experience with validation documentation and testing activities.
• Familiarity with electronic quality management and document management systems.
• Strong technical writing and communication skills.

Responsibilities

• Execute CSV activities for GxP systems.
• Develop and maintain validation documentation (URS, FS, IQ/OQ/PQ, etc.).
• Perform system impact assessments and risk-based validation.
• Support testing activities and defect tracking.
• Ensure compliance with FDA 21 CFR Part 11, GAMP 5, GMP, Data Integrity.
• Collaborate with Business, IT, QA, and Engineering teams.
• Support change controls, deviations, CAPAs, and reviews.
• Maintain validation records in electronic document management systems.
• Participate in internal audits and regulatory inspections.

Skills

Technical writing

Communication

GxP awareness

Regulatory knowledge

Education

Bachelor's degree in engineering, life sciences, pharmacy or related field

Tools

TrackWise

Veeva

SAP

LIMS

MES

Empower

SharePoint

ServiceNow

Jira

Job description

Job Description

We are seeking a CSV Specialist to support Computer System Validation (CSV) activities for GxP-regulated systems in the pharmaceutical, biotechnology, or medical device industry. The ideal candidate will be responsible for ensuring computerized systems are validated and compliant with regulatory requirements, company procedures, and industry standards.

Responsibilities

• Execute and support Computer System Validation (CSV) activities for GxP systems.
• Develop, review, and maintain validation documentation, including:
  • Validation Plans
  • User Requirements Specifications (URS)
  • Functional Specifications (FS)
  • Risk Assessments
  • IQ/OQ/PQ Protocols
  • Validation Reports
• Perform system impact assessments and risk-based validation activities.
• Support testing activities, including protocol execution and defect tracking.
• Ensure compliance with FDA 21 CFR Part 11, GAMP 5, GMP, and Data Integrity requirements.
• Collaborate with Business, IT, QA, and Engineering teams throughout the system lifecycle.
• Support change controls, deviations, CAPAs, and periodic reviews.
• Maintain validation records within electronic document management systems.
• Participate in internal audits and regulatory inspections.

Requirements

• Bachelor's degree in engineering, Computer Science, Life Sciences, Pharmacy, Biotechnology, or related field.
• 3+ years of CSV experience in a regulated pharmaceutical, biotechnology, or medical device environment.
• Knowledge of GAMP 5, FDA 21 CFR Part 11, GMP, and Data Integrity (ALCOA+) principles.
• Experience with validation documentation and testing activities.
• Familiarity with electronic quality management and document management systems.
• Strong technical writing and communication skills.

Preferred Qualifications

• Experience with CSA (Computer Software Assurance) methodologies.
• Knowledge of systems such as:
  • TrackWise
  • Veeva
  • SAP
  • LIMS
  • MES
  • Empower
  • SharePoint
  • ServiceNow
  • Jira
• Experience supporting regulatory audits and inspections.