Commissioning and Qualification Program Lead - Pharmaceutical Site Build

Job Type
Location
Richmond, Virginia
Salary
US$120 - US$140 per hour + *negotiable
Job Ref
BBBH2321072_1774294965
Date Added
March 23rd, 2026
Consultant
rebecca schopfer

We are looking for an experienced Commissioning and Qualification Program Lead, to join our client's team in Richmond, Va for a long term project! Our client is a global leading pharmaceutical company building a new facility. This is 12 month+ contract set to go the length of the project, up to 5 years. Requirements include:

  • 15+ years developing and delivering C+Q programs for Greenfield sites
  • Managing scope, budget, schedule, hiring, performance of C+Q teams
  • Connecting cross-functionally with different groups (quality, EPCM firms, subcontractors)
  • Coming from pharmaceutical build background
We look forward to hearing from you!
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.

Responsibilities:

  • Lead and coordinate commissioning and qualification (C&Q) activities to ensure project scope, schedules, and budgets are delivered as planned.
  • Manage and support the C&Q team's daily execution, providing technical direction and problem‑solving as needed to meet project milestones.
  • Plan and oversee FAT activities, including test strategy development, documentation, and on‑site execution coordination.
  • Collaborate with construction, automation, quality, project management, and end users to align system requirements and execution expectations.
  • Ensure compliance with GMP, regulatory requirements, internal policies, and site safety standards throughout all phases of C&Q work.
  • Facilitate training for internal teams and vendors on C&Q processes, ASTM E2500 methodology, and use of electronic validation systems such as Kneat.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.

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