QC Connectivity & Validation Specialist

R&D Partners; Waterford; On-site; EUR 45,000 - 65,000; Full time

Job summary

R&D Partners in Ireland seeks a QC Connectivity Compliance Specialist to lead validation and connectivity activities for pharmaceutical QC equipment. The role emphasizes regulatory compliance, documentation, and cross-functional collaboration across engineering, IT, and external suppliers.

The ideal candidate will have 2–3 years in QC validation, hands-on lab experience, and knowledge of QC bench equipment connectivity. The position is contract-based and requires eligibility to work in Ireland.

Qualifications

• Review validation documentation (protocols, reports, risk assessments) within defined timelines.
• Coordinate development of validation quality documents for regulatory compliance.
• Document deviations, non-conformances, and corrective actions with proper evaluation.
• Raise and coordinate Change Control Requests (CCRs) for project work with regulatory impact assessment.

Responsibilities

• Ensure compliance with FDA and EMA guidelines across all validation activities.
• Collaborate with cross-functional teams including engineering, IT, and suppliers.
• Identify process improvements in qualification and validation procedures.
• Support multiple validation projects concurrently with timelines and budgets.

Skills

QC Validation

Quality Systems

FDA/EMA Knowledge

Tools

CSV Principles

Calibration & Metrology

Job description

R&D Partners in Ireland seeks a QC Connectivity Compliance Specialist to lead validation and connectivity activities for pharmaceutical QC equipment. The role emphasizes regulatory compliance, documentation, and cross-functional collaboration across engineering, IT, and external suppliers.

The ideal candidate will have 2–3 years in QC validation, hands-on lab experience, and knowledge of QC bench equipment connectivity. The position is contract-based and requires eligibility to work in Ireland.