GMP Validation & Compliance Specialist

Claran Consultants Ltd; Carlow; On-site; EUR 60,000 - 85,000; Full time

Job summary

Claran Consultants Ltd is seeking a Compliance Specialist (Validation) for a leading pharmaceutical company in Carlow to provide compliance support across validation activities in a cGMP environment.

You will contribute to audits, maintain validation master plans, and drive continual improvement, ensuring regulatory requirements are met and that documentation is accurate and ready for inspection.

Qualifications

• Relevant technical qualification in Applied Pharmaceutical / Biological / Chemical sciences or engineered qualification.

Responsibilities

• Provide compliance support for validation activities.
• Support Regulatory, Divisional and Internal audits.
• Maintain site Validation Master Plan.
• Generate & approve periodic revalidation plan and report.
• Generate & approve periodic review plan.
• Review validation documentation.
• Investigate & RCA support.
• Ensure compliance with QMS, regulations and company standards.

Skills

Deviation Management

Change Control

Validation Lifecycle

QMS & GMP Compliance

Communication Skills

Problem Solving

Audits

Data Analysis

Education

Applied Pharmaceutical/Biological/Chemical sciences degree

Engineering qualification

Tools

DeltaV

Pi System

MS Office

Job description

Claran Consultants Ltd is seeking a Compliance Specialist (Validation) for a leading pharmaceutical company in Carlow to provide compliance support across validation activities in a cGMP environment.

You will contribute to audits, maintain validation master plans, and drive continual improvement, ensuring regulatory requirements are met and that documentation is accurate and ready for inspection.