Validation Engineer - GMP Pharma Equipment Mapping

Ellab; Limerick; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Benefits dieser Stelle

Company Pension - Employer matches 5%

Employee Assistance Programme

Professional development opportunities

Zusammenfassung

Ellab Ireland is seeking a Validation Engineer for our Limerick area. You will set up equipment, author and review validation documents, and perform temperature mapping in a sterile manufacturing environment.

The role requires 2–5 years of validation experience, a 3rd level qualification in Engineering/Pharmaceutical Science, and fluent English. Training is provided, with strong GMP exposure and a collaborative culture.

Qualifikationen

• 3rd level qualification in Engineering/Pharmaceutical Science or similar.
• 2–5 years of relevant Validation experience.
• Fluent spoken and written English.
• Knowledge of GMP.
• Be able to work on your own initiative.
• Attention to detail with a common-sense approach to problem solving.

Aufgaben

• Set up of Ellab equipment.
• Author, review, approve and execute validation documentation including protocols, summary reports, procedures, other lifecycle documents.
• Perform temperature mapping and validation of equipment such as autoclaves, fridges, freezers, incubators, stability cabinets in a sterile manufacturing environment.
• Analyse and interpret data from qualification studies and determine if it meets acceptance criteria.
• Troubleshooting customer and Ellab equipment.
• Reading P&ID’s effectively and following SOP’s.

Kenntnisse

Attention to detail

Self-motivation

Problem solving

English proficiency

Ausbildung

3rd level qualification in Engineering/Pharmaceutical Science

Jobbeschreibung

Ellab Ireland is seeking a Validation Engineer for our Limerick area. You will set up equipment, author and review validation documents, and perform temperature mapping in a sterile manufacturing environment.

The role requires 2–5 years of validation experience, a 3rd level qualification in Engineering/Pharmaceutical Science, and fluent English. Training is provided, with strong GMP exposure and a collaborative culture.