W2 Role :- Commissioning and Qualification Program Lead

Richmond, VA, US • Posted 2 days ago • Updated 2 days ago
Contract Independent
Contract W2
No Travel Required
On-site
Depends on Experience
Fitment

Dice Job Match Score™

🛠️ Calibrating flux capacitors...

Job Details

Skills

  • Automated Testing
  • Clarity
  • Logistics
  • Communication
  • Leadership
  • Performance Metrics
  • Management
  • Pharmaceutics
  • Project Delivery
  • Project Management
  • Sourcing
  • System Requirements
  • Team Building
  • Test Cases
  • Test Equipment
  • Commissioning and Qualification Program Lead
  • C+Q programs
  • pharmaceutical
  • ASTM E2500

Summary

Commissioning and Qualification Program Lead

Location: Richmond, Virginia (ONSITE) (RELOCATION OPEN)

Interview: Virtual

Multi-year project

 

MANAGER NOTES:

15+ years developing and delivering C+Q programs for greenfield sites
Managing scope, budget, schedule, hiring, and performance of C+Q teams
Connecting cross-functionally with different groups (quality, EPCM firms, subcontractors)
Coming from a pharmaceutical background

 

Primary Responsibilities

  • Provide strategic leadership for all C&Q activities, ensuring scope, timelines, and budgets are consistently met.
  • Direct day‑to‑day performance of the C&Q team and offer technical guidance to support successful project delivery.
  • Develop and oversee FAT planning, test case creation, and all field execution logistics.
  • Partner closely with construction, automation, QA, project management, and end‑user groups to maintain alignment on system requirements and delivery expectations.
  • Maintain adherence to GMPs, regulatory standards, internal procedures, and overall project safety practices.
  • Lead training sessions for internal teams and external vendors on C&Q methodology, ASTM E2500 processes, and Kneat system usage.
  • Coordinate the sourcing, readiness, and deployment of test equipment and field support resources.
  • Communicate progress, risks, and performance metrics to project leadership with clarity and consistency.
  • Drive timely escalation and resolution of technical issues to keep projects moving efficiently.

 

Qualifications

  • Bachelor’s degree in Engineering or equivalent practical experience.
  • 15+ years of experience delivering C&Q efforts for large pharmaceutical programs.
  • Proven track record supporting full‑lifecycle delivery of both Greenfield and Brownfield facilities.
  • Strong team‑building, leadership, and communication skills.
  • Expertise in GMPs, regulatory frameworks, commissioning, qualification, and ASTM E2500 practices.
  • Hands‑on proficiency with Kneat or similar electronic C&Q/validation platforms.
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: 91143216
  • Position Id: 8927326
  • Posted 2 days ago
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