PAS-X MES Engineer — Pharma Manufacturing & Compliance

Horizon Controls Group; Swords; Vor Ort; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

HorizonControls Group in Ireland seeks a Werum Pas-X Engineer to implement, configure, and maintain the Pas-X MES for client production sites. You will ensure compliant, efficient manufacturing processes and participate in validation activities.

The ideal candidate has strong MES expertise, pharma manufacturing knowledge, and experience with regulatory standards such as FDA, GMP and GAMP5, working with cross-functional teams to optimise workflows.

Qualifikationen

• Bachelor’s degree in engineering, CS, IT, or a related field.
• Certifications in MES or Pas-X are a plus.
• Proven experience with Werum Pas-X MES in pharma/biotech environments.
• Knowledge of pharma manufacturing processes including batch processing, packaging, and quality control.
• Experience with system integration and interfacing with ERP/SCADA and other manufacturing systems.

Aufgaben

• Configure and customize the Werum Pas-X MES according to production requirements.
• Participate in system deployment, testing, and validation in alignment with pharmaceutical industry regulations.
• Provide technical support for the Pas-X MES, including diagnosing and resolving issues.
• Perform periodic system updates and maintenance to ensure optimal performance.
• Collaborate with cross-functional teams to analyse and improve manufacturing workflows and develop EBRs.

Kenntnisse

Pas-X configuration

SQL/Java

GMP/GAMP5 knowledge

Analytical skills

Communication skills

Detail-oriented

Ausbildung

Bachelor’s degree in engineering, CS, IT or related field

Certifications in MES or Pas-X (nice to have)

Jobbeschreibung

HorizonControls Group in Ireland seeks a Werum Pas-X Engineer to implement, configure, and maintain the Pas-X MES for client production sites. You will ensure compliant, efficient manufacturing processes and participate in validation activities.

The ideal candidate has strong MES expertise, pharma manufacturing knowledge, and experience with regulatory standards such as FDA, GMP and GAMP5, working with cross-functional teams to optimise workflows.