Project Manager (CSV, Validation and Pharmaceuticals)

New York, NY, US • Posted 2 hours ago • Updated 2 hours ago
Contract Independent
Contract Corp To Corp
Contract W2
No Travel Required
Able to Sponsor
On-site
Depends on Experience
Fitment

Dice Job Match Score™

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Job Details

Skills

  • MES
  • GMP
  • GDP
  • Pharmaceuticals
  • quality
  • Validation
  • Computerized System Validation
  • SCADA
  • Regulatory Compliance
  • Traceability Matrix
  • Project Delivery
  • Pipeline Management
  • PMO
  • Continuous Improvement
  • FOCUS
  • Programmable Logic Controller
  • Documentation

Summary

Job Title: Project Manager  (Pharmaceuticals, CSV and Validation, MES/Scada/PLC/Automation)

Duration: 12 Months + Possible extension

Location: 100% onsite- Rensselaer, NY

Project Details:
Our client is undergoing modernization of their automation systems while aligning their IT and OT strategy, creating a need for stronger project management leadership within the Automation function.
They are seeking a Project Manager to lead and deliver multiple computerized system projects while also improving how projects are structured, managed, and executed. This individual will own project pipeline visibility, support the development of PMO frameworks, and drive greater consistency across project delivery.
The role includes drafting, reviewing, and approving validation and qualification documentation such as plans, specifications, protocols, traceability matrices, and summary reports. These efforts will support both new system implementations and enhancements to existing systems on a global scale.
This person will work cross-functionally with Automation, Quality, IT, and Engineering teams, acting as a bridge between technical and compliance functions to ensure successful, compliant, and scalable project outcomes. The position requires a strong balance of technical execution and quality oversight, along with a focus on continuous improvement and adoption of CSA principles.

Musts:
  • Experience leading computerized system or automation projects within regulated environments
  • Strong validation experience (plans, protocols, traceability matrices, summary reports)
  • Proven ability to work cross-functionally across Quality, IT, Engineering, and Automation teams

Pluses:
  • Experience supporting IT/OT integration or automation modernization initiatives
  • Exposure to PMO development, project pipeline management, or process standardization
  • Familiarity with CSA (Computer Software Assurance) principles
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10427688
  • Position Id: 8931265
  • Posted 2 hours ago
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