Pharma Facilities Engineer: cGMP Utilities & HVAC

BioSpace; Ireland (WV); On-site; USD 41,000 - 84,000; Full time

Job summary

Regeneron in Raheen, Limerick (Ireland) is seeking a Facilities Engineer to provide engineering support to the Facilities Operations, Utilities and HVAC teams. You will build and specify cGMP utilities and related equipment, and manage small-to-mid sized projects.

You will assist in design reviews, site acceptance, installation, QA validation documentation, investigations of utility systems, and implement corrective actions.

Qualifications

• BS/BA in Mechanical Engineering with 5 years of experience in Pharma/Biotech.
• Senior Engineer: BS/BA with 5+ years of experience.
• Engineer: BS/BA with 2+ years of experience.

Responsibilities

• Building and specifying cGMP utilities, HVAC equipment, piping, ducting and controls.
• Managing small-to-mid sized projects related to utilities & HVAC equipment & services.
• Troubleshooting plant equipment issues and recommending corrective actions.
• Assisting in design review, site acceptance and installation of equipment.
• Supporting QA Validation with design documents and protocol execution.
• Investigations of utility systems and control system anomalies and safety incidents.
• Implementing corrective/preventative actions for equipment and maintenance processes.
• Preparing evaluations and test plans for modification/change control documentation.
• Interpreting P&IDs, layouts, wiring diagrams and specifications for maintenance and repairs.
• Maintaining a clean and safe working environment by enforcing procedures.

Skills

Analytical skills

Interpersonal skills

Adaptability

Prioritisation

Education

BS/BA in Mechanical Engineering

5 years of relevant experience

Job description

Regeneron in Raheen, Limerick (Ireland) is seeking a Facilities Engineer to provide engineering support to the Facilities Operations, Utilities and HVAC teams. You will build and specify cGMP utilities and related equipment, and manage small-to-mid sized projects.

You will assist in design reviews, site acceptance, installation, QA validation documentation, investigations of utility systems, and implement corrective actions.