CSV Consultant

Piper Companies is seeking an CSV Consultant for a 3‑month contract supporting a rapidly growing pharmaceutical company in Greenville, NC
. This organization is investing heavily in cutting‑edge manufacturing technology
, and this role plays a critical part in supporting and validating high‑tech automated systems across their GMP operations.

This position offers an opportunity to contribute immediately to impactful automation and validation initiatives, with standard onsite hours Monday–Friday, 8:00 AM – 5:00 PM EST.

• Troubleshoot, maintain, and support manufacturing equipment controlled by PLC and SCADA systems (Rockwell/Allen‑Bradley strongly preferred).
• Interpret ladder logic and support minor logic modifications under formal change control.
• Support building automation systems and environmental monitoring platforms.
• Author and execute CSV deliverables including Validation Plans, Risk Assessments, IQ/OQ/PQ protocols, and summary reports.
• Ensure alignment with GAMP, cGMP, data integrity standards, and site SOPs.
• Lead or support change control activities for automation and software systems.
• Provide technical oversight for MES (E ) applications and QMS tools (training provided if needed).
• Work independently, providing clear shift handovers and mentoring peers on troubleshooting best practices.

• 3–5 years of automation validation and CSV experience in a regulated pharma/biotech environment.
• 5+ years of experience in process/equipment qualification or controls engineering preferred.
• Strong hands‑on background with Rockwell/Allen‑Bradley PLC/HMI systems.
• Familiarity with SCADA systems and automation lifecycle development.
• Ability to interpret ladder logic and troubleshoot high‑speed automated equipment.
• Full CSV lifecycle understanding (requirements → testing → reporting).
• Risk‑based validation experience and solid knowledge of change control fundamentals.
• Preferred:
  Exposure to MES (E ), QMS applications, and cross‑functional engineering environments.

• Competitive salary range: $140,000 – $190,000 ($67/hr-$91/hr).
• Full benefits available (medical, dental, vision, 401(k)).
• Opportunity to support a high‑growth pharma company investing in state‑of‑the‑art technology.
• 3‑month contract
  , with potential for extension based on performance and project needs.

Automation Engineer, CSV Engineer, Computer System Validation, PLC, SCADA, Rockwell, Allen‑Bradley, MES, E , QMS, GAMP, cGMP, High‑Speed Equipment, Validation Engineer, Automation Lifecycle, Pharmaceutical Manufacturing, Greenville NC, Onsite Role, Contract Position

Applications will be open for at least 30 days from the posting date of 1/14.