ZipRecruiter

Log In

1

C&Q Engineer Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Scheduler (C&Q) Responsibilities: * Maintain integrated C&Q schedule (plan/actual/forecast)

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Scheduler (C&Q) Responsibilities: * Maintain integrated C&Q schedule (plan/actual/forecast)

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Scheduler (C&Q) Responsibilities: * Maintain integrated C&Q schedule (plan/actual/forecast)

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Project Scheduler (C&Q) Responsibilities: * Maintain integrated C&Q schedule (plan/actual/forecast)

PharmEng Technology Americas

PR · On-site

... Engineering, and Training to ensure that our clients can keep on providing the world with their ... URS, C&Q Plan, risk assessments), authoring protocols, execution of commissioning and qualification ...

Mentor Technical Group

Sr. C&Q Specialist

Juncos, PR · On-site

As a world leader in life science engineering and technical solutions, MTG has the knowledge and ... Collaborate with C&Q Engineers to develop and maintain commissioning and qualification procedures ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Support compliance activities related to pharmaceutical engineering and C&Q projects. * Partner with Project Execution and Engineering teams to support investigations and follow-up activities when ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Support compliance activities related to pharmaceutical engineering and C&Q projects. * Partner with Project Execution and Engineering teams to support investigations and follow-up activities when ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Familiarity with Commissioning & Qualification (C&Q) lifecycle methodologies. * Experience working with engineering contractors, design firms, and equipment suppliers. * Strong communication ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

... Validation (C&Q) activities within a GMP-regulated manufacturing environment. This role will ... Coordinate communication among Engineering, Quality, Manufacturing, Operations, and external ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

... Validation (C&Q) activities within a GMP-regulated manufacturing environment. This role will ... Coordinate communication among Engineering, Quality, Manufacturing, Operations, and external ...

JC Automation Corp

PR · On-site

$25 - $45/hr

You will work closely with engineering, automation, quality, and vendor teams throughout the ... Support Commissioning & Qualification (C&Q) activities for equipment and systems installed within ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Familiarity with Commissioning & Qualification (C&Q) lifecycle methodologies. * Experience working with engineering contractors, design firms, and equipment suppliers. * Strong communication ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... C&Q Specialist Position Summary The C&Q Specialist will support commissioning and qualification ...

next page

Showing results 1-20

All JobsC&Q Engineer Jobs

C Q Engineer information

See salary details

$10

$53

$86

How much do c&q engineer jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for c&q engineer in the United States is $53.13, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $75.96 per hour, depending on experience, location, and employer.

What are C&Q Engineers?

C&Q Engineers, or Commissioning and Qualification Engineers, are professionals who ensure that systems, equipment, and processes in industries like pharmaceuticals, biotechnology, and manufacturing meet regulatory standards and function as intended. They are responsible for planning, executing, and documenting commissioning (verifying that systems are installed and work correctly) and qualification (demonstrating that systems consistently produce results meeting predetermined criteria). Their work is critical for compliance with regulations such as Good Manufacturing Practice (GMP) and for ensuring product quality and safety.

What is the difference between C&Q Engineer vs Commissioning Technician?

AspectC&Q EngineerCommissioning Technician
CredentialsBachelor's degree in engineering or related field, certifications like PE or CQMTechnical diploma or associate degree, relevant certifications
Work EnvironmentDesign review, project planning, overseeing commissioning processesHands-on testing, equipment startup, field troubleshooting
Industry UsageUsed across industries like oil & gas, power, manufacturingPrimarily in field commissioning, installation projects

The C&Q Engineer typically handles planning, documentation, and oversight of commissioning activities, ensuring compliance and quality. In contrast, the Commissioning Technician focuses on executing testing, startup, and troubleshooting tasks on-site. Both roles are essential in the commissioning process but differ in responsibilities and level of involvement.

What is a C&I engineer job description?

A C&I (Control and Instrumentation) engineer designs, develops, and maintains control systems and instrumentation for industrial processes. They work with automation equipment, PLCs, and SCADA systems, often requiring knowledge of electrical and control engineering principles. The role involves troubleshooting, system integration, and ensuring safety and compliance standards are met.

What are the key skills and qualifications needed to thrive as a C&Q Engineer, and why are they important?

To thrive as a C&Q (Commissioning and Qualification) Engineer, you need a solid background in engineering or life sciences, with experience in commissioning, qualification, and validation in regulated industries such as pharmaceuticals or biotechnology. Familiarity with industry standards (like GAMP, ASTM E2500), validation protocols, and tools such as PLC/SCADA systems and document management software is crucial. Strong analytical thinking, attention to detail, and excellent communication skills help in problem-solving and collaborating with multidisciplinary teams. These skills ensure that facilities, systems, and equipment meet compliance requirements, supporting safe and reliable manufacturing operations.

How does a C&Q Engineer typically collaborate with cross-functional teams during commissioning and qualification projects?

As a C&Q Engineer, you'll work closely with process engineers, validation teams, project managers, and quality assurance personnel to ensure systems and equipment meet regulatory and client requirements. Collaboration often involves attending multidisciplinary meetings, aligning on project timelines, and sharing critical documentation. Effective communication is key, as you'll coordinate testing activities, resolve technical issues, and provide updates on project progress. This teamwork ensures that commissioning and qualification activities are executed efficiently and in compliance with industry standards.
More about C Q Engineer jobs
What job categories do people searching C&Q Engineer jobs look for? The top searched job categories for C&Q Engineer jobs are:
C Q Engineer jobs near you
Infographic showing various C&Q Engineer job openings in the United States as of May 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $110,519 per year, or $53.1 per hour.

Project Scheduler (C&Q)

Validation & Engineering Group, Inc

PR

Full-time

Posted yesterday

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.

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

  • Project Scheduler (C&Q)

Responsibilities:

  • Maintain integrated C&Q schedule (plan/actual/forecast).
  • Support schedule impact analysis for C&Q reporting.
  • Align with document preparation and execution phases and provide inputs for weekly/monthly forums.
  • Escalate any concerns or issues that may be impacting the C&Q schedule.
  • Work closely with the Project Integrator to ensure the latest updates on C&Q activities are captured and to stay current with changes in the overall project schedule.
  • Run schedule scenarios as needed and assess/communicate impacts to the C&Q schedule.

Qualifications:

  • Experience developing and maintaining integrated schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.
  • Proficiency with scheduling tools (e.g., Primavera P6 and/or Microsoft Project) and schedule controls practices (baseline management, progress updates, forecasting).
  • Ability to perform schedule impact analysis and communicate drivers/risks for C&Q reporting (weekly/monthly).
  • Strong coordination skills to align schedule with document readiness (protocols, test scripts, turnover packages) and field execution.
  • Clear written and verbal communication; able to support forums and produce schedule visuals/metrics as needed.

Additional Preferences:

  • Prior experience supporting CQV deliverables and turnover/handshake processes in GMP/regulated environments.
  • Familiarity with progress measurement for C&Q (e.g., protocol readiness, execution, deviations/punchlist closure) and dashboard reporting.
  • Experience working onsite and coordinating with construction, QA, engineering, and C&Q leads.

Qualifications:

  • Bachelor's Degree in Science or Engineering.
  • Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Technical Writing skills and investigations processes.
  • Available to work extended hours, possibility of weekends and holidays.

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.

#LI-ZL1