Find a jobRecruiters

CQV Engineer

Exclusive opportunity

Onsite

CQV Engineer

Stark Pharma Solutions Inc

CQV Engineer

2 months ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

Important information


Contract type:

Freelance / Contract

Location:

Charlotte, NC, USA

Work mode:

Onsite

Published on:

5 September 2026

What they need


About The Company Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Position: CQV Engineer

Location: North Carolina

Duration: Long Term

Job Overview We are seeking a CQV Engineer with strong experience in pharmaceutical manufacturing and regulated environments to support commissioning, qualification, and validation activities for facilities, utilities, equipment, and systems.

Key Responsibilities Develop, execute, and document commissioning and qualification protocols.

Perform IQ, OQ, and PQ activities for equipment, utilities, and systems.

Support commissioning and qualification of pharmaceutical manufacturing facilities and equipment.

Prepare and maintain CQV protocols, reports, and validation documentation.

Support FAT, SAT, commissioning, and qualification activities.

Work with Engineering, Quality, Manufacturing, and Project teams to resolve CQV issues.

Support deviations, investigations, change controls, and CAPA activities.

Ensure CQV activities comply with GMP, FDA, and GxP requirements.

Support continuous improvement and project execution activities.

Required Qualifications Bachelor s degree in Engineering, Life Sciences, or a related technical field.

3+ years of experience in CQV, Commissioning, Qualification, or Validation within the pharmaceutical or biotech industry.

Hands-on experience with IQ/OQ/PQ activities.

Experience with pharmaceutical facilities, utilities, equipment, or systems.

Knowledge of GMP, FDA, GxP, and validation requirements .

Experience preparing and executing CQV protocols and reports.

Strong documentation, analytical, communication, and problem-solving skills.

Ability to work effectively with cross-functional teams.

How To Apply Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse

backgrounds.

Other offers great for you!

These companies are also looking for great profiles

Futurwork

Cloud engineer

550 - 600€

Freelance

Brussels, Belgium

Hybrid

Skills

IBM CloudAnsibleTerraform

21 hours ago

Quick apply

Kalytech Consulting

Automation Engineer

540€

Freelance

Leuven, Belgium

Hybrid

Skills

PythonAnsibleautomationpowershell

20 hours ago

Quick apply

Espace Freelance

AI Engineer confirmé

Freelance

Paris, France

Hybrid

Skills

Google Cloud PlatformPythonVertex AIRAGLangChainAI agents

3 hours ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools