CQV Engineer

Stark Pharma Solutions Inc

Charlotte (NC)

On-site

USD 90,000 - 130,000

Full time

6 days ago
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Job summary

Stark Pharma Solutions Inc. is 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.

The role collaborates with Engineering, Quality, Manufacturing, and Project teams to develop, execute CQV protocols (IQ/OQ/PQ) and ensure compliance with GMP, FDA, and GxP requirements, while driving continuous improvement projects.

Qualifications

  • 3+ years of experience in CQV, commissioning, qualification, or validation in pharmaceutical/biotech.
  • Hands-on IQ/OQ/PQ experience.
  • Experience with CQV protocols and reports.
  • Knowledge of GMP, FDA, GxP regulations and validation.
  • Strong documentation, analytical, and communication skills.
  • Ability to work with cross-functional teams.

Responsibilities

  • Develop, execute, and document commissioning and qualification protocols.
  • Perform IQ, OQ, 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.

Skills

Documentation
Analytical skills
Communication
Problem solving
Cross-functional collaboration

Education

Bachelor's degree in Engineering, Life Sciences, or related technical field

Job description

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.

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

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