C

CAI

Operational readiness consulting for pharma

Automation Equipment Support Engineer

Controls & Automation EngineeringConfirmed live in the last 24 hours
Full-timeLimerick, IrelandNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Automation Engineering, Electrical Engineering, Mechatronics, Computer Systems Engineering, or a related discipline.
  • Approximately 3-6 years of experience in a pharmaceutical, biotechnology, medical device, or other regulated manufacturing environment.
  • Experience supporting automated process equipment in a production environment.
  • Working knowledge of programmable logic controller, human-machine interface, and supervisory control and data acquisition systems.
  • Experience with one or more of the following platforms: DeltaV; Siemens PCS7 or TIA Portal; Rockwell or Allen-Bradley; FactoryTalk; or Wonderware.
  • Familiarity with current good manufacturing practice requirements, deviations, corrective and preventive actions, and change control processes.
  • Ability to troubleshoot and solve problems in a fast-paced manufacturing environment.
  • Ability to work cross-functionally with operations, maintenance, engineering, and quality teams.

Responsibilities

  • Provide day-to-day automation support for good manufacturing practice manufacturing equipment and process systems.
  • Troubleshoot and resolve programmable logic controller, human-machine interface, supervisory control and data acquisition, and controls-related issues to minimize production downtime.
  • Support operations, maintenance, engineering, and quality teams during investigations, deviations, and technical escalations.
  • Execute and support automation changes through established change control processes.
  • Participate in root cause investigations and implement corrective and preventive actions.
  • Support equipment upgrades, system enhancements, and continuous improvement initiatives.
  • Assist with commissioning, qualification, and validation activities for new and existing equipment.
  • Maintain automation documentation, system lifecycle records, and technical specifications in compliance with good manufacturing practice requirements.
  • Contribute to improving equipment reliability, performance, and operational efficiency.

Desired Qualifications

  • Biologics, vaccine, or large-scale pharmaceutical manufacturing experience.
  • Exposure to commissioning, qualification, and validation activities.
  • Experience supporting process equipment such as bioreactors, cleaning-in-place and steam-in-place systems, chromatography skids, filtration systems, utilities, or filling equipment.
  • Understanding of Good Automated Manufacturing Practice 5 and data integrity principles.

About the Company

CAI

Operational readiness consulting for pharma

CAI Technical Consulting Malaysia SDN (brand cagents.com) provides operational readiness consulting for pharmaceutical, biotech, and healthcare firms. It helps clients prepare for full-scale production through quick operational readiness assessments, gap-tailored plans, and hands-on implementation support in areas like project planning, production operations, asset management, reliability, and sustainability, plus Digital Pathology Validation for Leica Biosystems to meet regulatory standards. The firm differentiates itself by combining rapid assessments with practical, cost-effective strategies, ongoing industry collaboration, and global delivery that informs tailored solutions. Its goal is to help clients accelerate their path to compliant, scalable operations and successful production scale-up.

Company size
1,001-5,000
Company stage
Pre-seed
Total funding
$3.4M
Headquarters
Indianapolis, IN
Founded
1996

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