CQV Engineer
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Job Location:
Monthly Salary:
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job Summary
Argo-X
ArgoX is a specialist consultancy that delivers flexible highimpact staffing to pharma biotech medicaldevice and diagnostics companies worldwide. Our consultants operate in GxP environments helping clients accelerate product development while staying fully compliant with evolving regulations.
Tasks
Develop and execute qualification and validation plans for instruments utilities and production lines.
- Author and review protocols test scripts and final reports ensuring traceability and compliance.
- Perform risk assessments define acceptance criteria and manage change control.
- Support auditors during inspections and provide evidence of validated state.
- Mentor client staff on best practices and maintain validation documentation libraries.
Requirements
BSc/MSc in Engineering Chemistry Biotechnology or related field.
- Minimum 4years of handson CQV experience in GMPregulated environments.
- Strong familiarity with EU Annex15 FDA 21CFR211 and riskbased validation concepts.
- Proficient in writing IQ/OQ/PQ protocols reports and deviation investigations.
- Ability to travel to client sites (Europe) and work under tight timelines.
Join Us! Why ArgoX
Join a network where your expertise is matched to highvisibility projects that shape the future of healthcare. Enjoy flexible assignments competitive rates and continuous professional development.
Key Skills
- ASP.NET
- Health Education
- Fashion Designing
- Fiber
- Investigation
