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Validation & Engineering Group, Inc
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Validation & Engineering Group, Inc

Commissioning & Qualification (C&Q) Specialist / Engineer

TX, United States
OH, United States
NC, United States
SC, United States
GA, United States

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Job details

Experience: 3+ years of experience in commissioning, qualification, validation, engineering, or a related field.
Posting language: English
Posted: Sep 18, 2026

Original job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

This posting is for future opportunities which could be onsite or hybrid. While this is not tied to an immediate opening, we actively review submissions and connect with candidates as project needs arise.

Commissioning & Qualification (C&Q) Specialist / Engineer

We are seeking Commissioning & Qualification (C&Q) Specialists and Engineers with experience in pharmaceutical, biotechnology, medical device, or other regulated life sciences environments.

Responsibilities:

Support commissioning, qualification, and validation activities for equipment, utilities, facilities, systems, and processes.
Develop, review, and execute C&Q documentation, including URS, risk assessments, FAT/SAT, IQ/OQ/PQ, protocols, and reports.
Support equipment/system startup, troubleshooting, testing, and turnover.
Work closely with Engineering, Quality, Validation, Manufacturing, Automation, and Project Management teams.
Ensure activities comply with GMP, FDA, ISO, and applicable industry standards.
Support deviations, change controls, and other project documentation as needed.

Qualifications:

Bachelor's degree in Engineering, Life Sciences, or related technical field preferred.
3+ years of experience in commissioning, qualification, validation, engineering, or a related field.
Experience in pharmaceutical, biotech, medical device, or GMP-regulated environments.
Knowledge of IQ/OQ/PQ, FAT/SAT, risk assessments, and validation documentation.
Strong technical writing, communication, and problem-solving skills.
Ability to work effectively in cross-functional project teams.

Experience with manufacturing equipment, process systems, utilities, facilities, automation, laboratory equipment, or computerized systems is highly valued.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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More about this job

Skills

Biotechnology
Documentation
SAP IQ
Troubleshooting
Project management
Good manufacturing practices
Technical writing
Communication skills
Problem solving
Laboratory equipment

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