Become a QC Validation Specialist at a leading pharmaceutical company in Waterford. This hybrid role allows for flexible working, focusing on quality documentation and compliance management in a highly regulated environment.
CareerWise Recruitment is looking for a talented QC Validation Specialist for a 23-month contract within a Waterford pharmaceutical firm. Candidates will work hybrid, with three days on-site and two days at home, coordinating essential validation activities. Responsibilities include reviewing quality documentation, managing deviations, and ensuring compliance with regulatory standards, including FDA and EMA.
Key Responsibilities:
• Approve validation documentation including reports and risk assessments
• Manage and document deviations and corrective actions




• Ensure strong adherence to quality compliance standards
• Develop validation documents while managing CCRs
• Oversee QC bench equipment connectivity requirements
Requirements:
• 2-5 years of QC validation experience in the industry
• Comprehensive knowledge of QC operations in pharmaceuticals
• Proficient in regulatory guidelines and compliance standards
• Experience with validation and qualification activities
• Understanding of risk assessment and traceability
Leverage your expertise in QC to ensure regulatory compliance and enhance quality operations in a energetic organization.
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📌 QC Validation Specialist Hybrid Role (Kingston)
🏢 CareerWise Recruitment
📍 Kingston