Automation Engineer

Qcs Staffing

The Role

Overview

Support downstream process automation DeltaV in a cGMP pharma facility

Key Responsibilities

  • kneat docs
  • automation design
  • document review
  • lifecycle docs
  • capex delivery
  • project meetings

Tasks

-Support generation of Kneat documents. -Initiate design and provide input on Automation requirements for one or multiple process areas -Review and approve Kneat documents including: DeltaV software FATs, Automation Commissioning Test Protocols, software OQs, and Automation Change Assessments. -Review life cycle documentation -Initiate and drive delivery of Automation changes in support of CAPEX project requirements -Attend regularly scheduled project status meetings with Automation engineers and the System Integrator

Requirements

  • cgmp
  • fda
  • automation
  • kneat
  • communication
  • teamwork

What You Bring

-Experience in a cGMP pharmaceutical facility working with FDA regulations is required -Ability to own and implement Automation change controls independently -Excellent organizational, oral, and written communication skills and fluency in English with the ability to effectively communicate within cross-functional teams and to management -Excellent interpersonal skills and ability to work effectively and efficiently in a team-based environment with employees at all levels -Working knowledge of Kneat validation software is required

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