Join a Waterford pharmaceutical company as a QC Compliance Specialist in a hybrid role. This position covers validation documentation, compliance evaluations, and improvement coordination with a focus on quality control operations.

CareerWise Recruitment is seeking a QC Compliance Specialist for a 23-month contract. This hybrid role allows for three days on-site and two days from home. You will review validation documentation, manage deviations, and ensure compliance with FDA and EMA standards while leveraging your experience in QC bench equipment and CSV validation.

Key Responsibilities:
• Review and approve validation documents and protocols
• Document deviations and corrective actions effectively
• Raise Change Control Requests (CCRs) ensuring proper documentation




• Ensure compliance with FDA, EMA, and company standards
• Coordinate validation quality documents development

Requirements:
• 2-5 years in QC validation and quality systems
• Experience in pharmaceutical industry quality control
• Hands-on experience with QC bench equipment
• Solid knowledge of CSV and regulatory standards
• Familiarity with risk assessment methodologies

Utilize your regulatory knowledge, validation experience, and QC expertise to impact compliance and quality in the pharmaceutical sector.
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📌 QC Compliance Specialist in Waterford (Ontario)
🏢 CareerWise Recruitment
📍 Ontario