~19d ago

Commissioning & Qualification (C&Q) Specialist / Engineer

OtherEngineer
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Quick Summary

Key Responsibilities

Support commissioning, qualification, and validation activities for equipment, utilities, facilities, systems, and processes. Develop, review, and execute C&Q documentation, including URS,

Requirements Summary

Support commissioning, qualification, and validation activities for equipment, utilities, facilities, systems, and processes. Develop, review, and execute C&Q documentation, including URS,

Technical Tools
OtherEngineer

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.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • 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.

Location & Eligibility

Where is the job
United States
On-site within the country
Who can apply
US

About this job

Who can apply
United States
Posted
19 days ago
Employer
has 203 open jobs on Jobera in 2 countries.

Listing Details

First seen
September 26, 2026
Last seen
October 15, 2026

Posting Health

Days active
18
Repost count
0
Trust Level
25%
Scored at
October 15, 2026

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Commissioning & Qualification (C&Q) Specialist / Engineer