QC Validation Specialist Hybrid Role

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.

Career Wise 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 dynamic organization.
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