Senior CQV Engineer: Validation & Compliance Lead

DPS Group Global; South Dublin; Sur place; EUR 80 000 - 110 000; Plein temps

Résumé du poste

DPS Group Global is seeking an experienced Validation Engineer to support commissioning, qualification, and validation activities in a GMP-regulated pharmaceutical environment. The role focuses on ensuring equipment, facilities, utilities, computerised systems, and manufacturing processes meet cGMP and regulatory requirements.

You will prepare and review validation documentation, manage deviations and change controls, and coordinate quality-driven validation activities across projects to

Qualifications

• Bachelor’s degree in engineering/science or related field.
• 5+ years in pharma manufacturing, Validation, Engineering or Operations.
• Experience with GMP documentation and risk-based validation.

Responsabilités

• Prepare, review, and approve validation docs for equipment, facilities, utilities, and systems.
• Support projects from design through commissioning, qualification, and validation.
• Review and approve C&Q documentation.
• Manage deviations, punch lists, and change controls.
• Coordinate vendors during commissioning and qualification activities.
• Maintain validation schedules and project timelines.
• Ensure compliance with cGMP, data integrity, and regulatory requirements.
• Promote a strong quality and compliance culture on site.

Connaissances

Validation & Qualification

cGMP Compliance

Change Control

Deviation Management

Risk Assessments

Technical Writing

Vendor Management

Project Planning

Attention to Detail

Stakeholder Management

Formation

Bachelor's Degree in Engineering, Science, or related technical discipline

Outils

Kneat

Veeva

TrackWise

Description du poste

DPS Group Global is seeking an experienced Validation Engineer to support commissioning, qualification, and validation activities in a GMP-regulated pharmaceutical environment. The role focuses on ensuring equipment, facilities, utilities, computerised systems, and manufacturing processes meet cGMP and regulatory requirements.

You will prepare and review validation documentation, manage deviations and change controls, and coordinate quality-driven validation activities across projects to