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CQV Engineer

Job in Charlotte, Mecklenburg County, North Carolina, 28245, USA
Listing for: Stark Pharma Solutions Inc
Full Time position
Listed on 2026-09-10
Job specializations:
  • Engineering
    Validation Engineer, Pharma Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

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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