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CSV Specialist

Katalyst Healthcares & Life Sciences

Harrisburg, PA

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JOB DETAILS
SKILLS
Atlassian JIRA, Biology, Biotech and Pharmaceutical, Bug Tracking/Defect Management, Change Control, Code of Federal Regulations, Communication Skills, Computer Science, Computer Skills, Computer Software, Computer Systems, Data Quality, Document Management, Electronic Document and Records Management System (EDRMS), FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), GxP, Industry Standards, Information Technology & Information Systems, Internal Audit, Laboratory Information Management System (LIMS), Maintain Compliance, Medical Equipment, Microsoft SharePoint, Pharmacy, Process Validation, Quality Assurance, Quality Management, Record Keeping, Regulations, Regulatory Requirements, Risk, Risk Analysis, SAP, ServiceNow, System Lifecycle, System Validation, Systems Analysis, Technical Writing, Validation Documentation, Validation Plan, Validation Testing, Writing Skills
LOCATION
Harrisburg, PA
POSTED
10 days ago
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.


About the Company

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Katalyst Healthcares & Life Sciences