CQV Lead (cGMP - Pharmaceutical)

Sorry, this job was removed at 03:02 p.m. (UTC) on Tuesday, Jul 28, 2026
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2 Locations
In-Office
146K-205K Annually
Expert/Leader
Other • Professional Services • Consulting
Building Value Through Expertise
The Role
Lead commissioning, qualification, and validation activities for GMP capital projects. Develop and approve C&Q and validation documentation, oversee contractors and automation/computerized systems, drive risk-based qualification strategies, and coordinate deliverables across engineering, QA, automation, and operations to ensure regulatory alignment and operational readiness.
Summary Generated by Built In

At Cumming Group, you will work on some of the world's most exciting projects in a dynamic environment where your success is measured by the impact you make. We are one of the fastest-growing project and cost management consultancies in the United States, as reflected in our top 10 rankings in ENR. With over 60 offices globally, an extremely diverse project portfolio, and double-digit year-over-year revenue growth, the opportunities to make your mark are limitless!

We are currently looking for a Commissioning and Qualification Lead in the Greater Boston, MA area. This role will support complex GMP capital projects, with a focus on C&Q strategy, validation execution, automation systems, and operational readiness.

This is a strong opportunity for someone with deep pharmaceutical C&Q experience who enjoys leading technical workstreams, coordinating contractors, and helping bring highly regulated manufacturing facilities and systems online.

Responsibilities:

  • Lead commissioning, qualification, and validation activities for GMP capital projects.

  • Develop, review, and approve C&Q plans, validation plans, protocols, reports, and related technical documentation.

  • Oversee C&Q contractors and technical workstreams supporting facilities, utilities, process equipment, automation, and computerized systems.

  • Drive risk-based qualification strategies, including acceptance criteria, testing requirements, documentation approach, and regulatory alignment.

  • Coordinate C&Q deliverables across engineering, QA, automation, IT, MS&T, construction, vendors, and site operations.

  • Support project schedules, budgets, milestone tracking, change controls, deviations, investigations, and CAPA activities.

  • Serve as a C&Q / validation subject matter expert during project reviews, audits, and stakeholder updates.

Technical Requirements:

  • Bachelor’s degree in Engineering, Life Sciences, Computer Science, or a related technical discipline required.

  • 10+ years of pharmaceutical, biotechnology, life sciences, or GMP manufacturing experience.

  • Strong background in commissioning, qualification, validation, and GMP project execution.

  • Experience in cell and gene therapy, biologics, advanced therapy manufacturing, or other highly regulated environments preferred.

  • Experience supporting large capital projects involving GMP facilities, utilities, process equipment, automation, and/or computerized systems.

  • Knowledge of PLCs, SCADA, DCS, MES, CSV, data integrity, 21 CFR Part 11, and GAMP 5.

  • Familiarity with ASTM E2500, FDA, EMA, ICH, Annex 11, and Annex 15 requirements.​

#LI-JB1

Cumming Group is committed to providing Equal Employment Opportunity in its personnel policies and practices. It is Cumming Group’s policy to recruit, hire, train and promote Team Members and applicants for employment without regard to race, color, creed, religion, age, sex, marital status, registered domestic partner status, genetic information, sexual preference, sexual orientation, gender (including gender expression and gender identity), pregnancy (including childbirth or related medical conditions, including breastfeeding), military service, national origin, ancestry, citizenship, physical disability, mental disability, veteran status or any other protected classification under federal, state, or local law. All such decisions are based on (1) individual merit, qualifications, and competence as they relate to the particular position, and (2) promotion of the principle of equal employment opportunity.

All other terms and conditions of employment, such as compensation, benefits, transfers, layoff, return from layoff, training, education, and social and recreational programs, are administered without regard to the characteristics described above. To this end, Cumming Group complies with all provisions of Title VII of the Civil Rights Act of 1964 as amended, all of the rules, regulations and relevant orders of the Secretary of Labor, and all similar state and local laws.


The salary range for this full-time role is $146,400.00-$204,933.36 per year. Ranges are determined based on the position, geography, client and industry experience and level, and represent a good faith effort to provide a fair and equitable salary. This range reflects base salary only, and not the total compensation package. Cumming Group reserves the right to pay more or less than the posted range, depending on a candidate’s experience, skills, and qualifications, including client requirements.

In addition to base salary, Cumming Group offers a comprehensive benefits package including:

  • Medical
  • Dental Insurance
  • Vision Insurance
  • 401(k)
  • 401(k) Matching
  • Paid Time Off
  • Paid Holidays
  • Short and long-term disability
  • Employee Assistance Program

Skills Required

  • Bachelor's degree in Engineering, Life Sciences, Computer Science, or related technical discipline
  • 10+ years pharmaceutical, biotechnology, life sciences, or GMP manufacturing experience
  • Strong background in commissioning, qualification, validation, and GMP project execution
  • Experience in cell and gene therapy, biologics, advanced therapy manufacturing, or other highly regulated environments
  • Experience supporting large capital projects involving GMP facilities, utilities, process equipment, automation, and/or computerized systems
  • Knowledge of PLCs, SCADA, DCS, MES, CSV, data integrity, and 21 CFR Part 11
  • Knowledge of GAMP 5
  • Familiarity with ASTM E2500, FDA, EMA, ICH, Annex 11, and Annex 15 requirements

Cumming Group Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cumming Group and has not been reviewed or approved by Cumming Group.

  • Healthcare Strength — Medical, dental, and vision insurance are core offerings, with mental-health support and HSA/FSA options also listed. The breadth of coverage is presented as a strong element of the package for a professional-services firm.
  • Wellbeing & Lifestyle Benefits — An employee assistance program, mental-health resources, commuter benefits, discounts, flexible scheduling, and team activities are included. These additions extend value beyond base pay and core insurance.
  • Parental & Family Support — Parental and family medical leave are explicitly part of the benefits. This support complements standard health coverage for employees with caregiving needs.

Cumming Group Insights

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The Company
HQ: New York, NY
Year Founded: 1996

What We Do

Cumming Group is an international project management and cost consulting company that delivers creative, customized solutions to a vast portfolio of clients worldwide.

Why Work With Us

Cumming Group’s mission is to be the most trusted team in the built environment. We maximize the value delivered to our clients by attracting team members who match our drive and client-centric focus. Our team members are exceptional problem-solvers who appreciate Cumming Group’s entrepreneurial culture that empowers them to achieve both personal

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