Job Title

• CSV Analyst Job Location
• WestPoint, PA (Hybrid, 3 days/week need to be on site) Mandatory Skills
• CSV ( Manufacturing Systems
• DeltaV,Rockwell,MES,PI etc),KNEAT,MEDS Job Description
• Hands-on experience supporting validation and compliance activities for computerized manufacture ng systems in a regulated pharmaceutical environment.

Provide CSV compliance support for Capital and Strategic Projects to ensure continuity of compliance oversight and project delivery. Develop, review, and approve validation lifecycle deliverables in accordance with GxP requirements, internal SOPs, and regulatory expectations. Provide compliance guidance to project teams on

SDLC, CSA

(Computer Software Assurance), qualification, risk-based validation, and change control processes. Strong experience in Computer System Validation (CSV) within GMP-regulated pharmaceutical/manufacturing environments. Knowledge of Validation Lifecycle, CSA, SDLC, Qualification (IQ/OQ/PQ), Change Control, CAPA, and Risk Management. Experience reviewing and approving validation documentation and compliance deliverables. Familiarity with GxP regulations, Data Integrity, FDA, EMA, and industry compliance requirements. Exposure to one or more manufacturing automation platforms including: Delta

V DCS PLC

systems (Rockwell and/or Siemens) Process Historians Laboratory Automation Systems Experience with validation, qualification, change control, risk assessments, and lifecycle compliance activities associated with manufacturing and laboratory computerized systems. Understanding of GxP, Data Integrity, CSV/CSA, and SDLC requirements for manufacturing automation platforms