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C&V Lead

Job in Mobile, Mobile County, Alabama, 36624, USA
Listing for: i-Pharm GxP
Full Time position
Listed on 2026-07-27
Job specializations:
  • Engineering
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 165312 - 247968 USD Yearly USD 165312.00 247968.00 YEAR
Job Description & How to Apply Below

Job Title

Commissioning & Qualification (C&Q) Lead

Location

Fully on-site - Alabama

Initial 12-month contract, with potential for extension based on performance Competitive W2 hourly rate plus reimbursable expenses Role Summary

The C&Q Lead is responsible for overall management of Commissioning & Qualification (C&Q) delivery, ensuring scope, schedule, budget, and quality standards are met. This role leads an integrated C&Q program throughout the project lifecycle from design through system handover using an ASTM E2500 Verification methodology and electronic validation tools such as Kneat.

Key Responsibilities
  • Manage the C&Q program, including scope, schedule, budget, and team performance.
  • Provide technical oversight and guidance to C&Q team members.
  • Plan and manage FATs, test case development, and field execution logistics.
  • Collaborate with project leadership, construction, automation, QA, and end-user teams to align on project scope and delivery strategy.
  • Ensure compliance with GMPs, regulatory requirements, and project safety procedures.
  • Train project teams and service providers on C&Q processes, ASTM E2500 Verification, and Kneat electronic validation systems.
  • Source and manage test equipment and craft support for field testing.
  • Report progress and metrics to project leadership.
  • Escalate unresolved issues promptly to maintain project momentum.
Requirements
  • BS in Engineering or equivalent experience.
  • 15+ years of C&Q experience in major pharmaceutical project delivery.
  • Experience managing Brownfield or Greenfield facility projects through full lifecycle.
  • Strong leadership, team management, and communication skills.
  • Knowledge of GMPs, regulatory requirements, commissioning, qualification, and ASTM E2500 Verification.
  • Hands-on experience with Kneat electronic C&Q/validation system.
Preferred Skills
  • Demonstrated ability to influence cross-functional teams and facilitate issue resolution.
  • Experience implementing integrated C&Q programs in pharmaceutical projects.
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