
CQV Engineer
Qcs Staffing
The Role
Overview
Execute CQV testing for small equipment in a sterile drug facility.
Key Responsibilities
- regulatory testing
- cqv documentation
- commissioning testing
- project documentation
- safety management
Tasks
-Responsible for ensuring GMP equipment are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations. -Development and execution of CQV testing documentation for benchtop, mobile, analytical, PAT, incubators, BSCs, and TCU equipment for the Sterile Drug product facility.( 100%) -Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation/electronic records for equipment, utilities assigned. -Responsible for ensuring that all equipment, is tested in compliance with project related standards from a commissioning perspective.
Requirements
- cqv
- automation
- project lifecycle
- teamwork
- safety
- budget
What You Bring
-Experience in CQV of Drug Substance/Drug product small equipment with integrated automation. -Demonstratable capacity to effectively execute the CQV testing approach for assigned from initiation to completion. -CQV project lifecycle experience from design through to C&Q and handover. -Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget.
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The Company
About Qcs Staffing
-Founded with the aim of providing top-tier staffing solutions for diverse sectors. -Focus on long-term partnerships with clients, ensuring the right talent for specialized roles. -Expert in recruiting for both large-scale projects and niche, high-demand sectors. -Has become a trusted partner in sectors such as Industrial, Energy, and Infrastructure. -Notable for a rapid response to market demands and changing industry trends. -Experience in delivering recruitment services for large infrastructure and energy projects. -Specializes in sourcing skilled professionals for both permanent and temporary roles. -Recognized for working on complex and large-scale projects with a diverse client base.
Sector Specialisms
Life Sciences
Renewable Energy
Data Centres
IT
Pharmaceutical
Biotech
Medical Device
Manufacturing
Science & Technology
IT / Automation
Pharmacovigilance / Regulatory / Medical Affairs
Construction / HSE
PMO / Project Controls
Compliance / Quality Assurance
Commissioning, Qualification and Validation (CQV)
Capital and Startup Projects
