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.

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