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 in office 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 dynamic organization.
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📌 QC Validation Specialist Hybrid Role (Ontario)
🏢 CareerWise Recruitment
📍 Ontario