QC Connectivity Compliance Specialist

We are currently looking for a QC Connectivity Compliance Specialist to join a leading pharmaceutical company in Co Waterford on an initial 12 month contract. This opportunity is ideal for a seasoned quality professional with expertise in validation, equipment connectivity, and compliance systems.


KEY DUTIES AND RESPONSIBILITIES

Your duties as the QC Connectivity Compliance Specialist will be varied however the key duties and responsibilities are as follows:

   • Oversee validation and qualification activities, including review and approval of validation documentation such as protocols, reports, risk assessments, and traceability matrices to ensure they meet regulatory standards.

   • Coordinate the development and maintenance of validation quality documents, with a focus on compliance with FDA, EMA, and internal quality standards.

   • Document, manage, and evaluate deviations, non-conformances, and corrective actions to uphold quality and regulatory integrity.

   • Lead Change Control Requests (CCRs) for validation projects, ensuring proper documentation, impact assessment, and regulatory compliance.

   • As the QC Connectivity Compliance Specialist, you will liaise with cross-functional teams to identify process improvements and support continuous validation and connectivity system enhancements.


ROLE REQUIREMENTS

To be successful in your application to this exciting role as the QC Connectivity Compliance Specialist we are looking to identify the following on your profile and past history:

   • A Degree or higher level in pharmaceutical sciences, biotechnology, chemistry, or a related field

   • Proven hands-on experience (minimum 2–3 years) in validation, qualification, and quality control operations within the pharmaceutical or biotech sectors

   • Strong knowledge of regulatory guidelines (FDA, EMA) related to validation and quality systems

   • Demonstrable experience with QC bench equipment connectivity and validation processes

   • Excellent project management, communication, and troubleshooting skills to support multiple validation projects simultaneously


Key Words: validation / QC / connectivity / compliance systems / regulatory standards / pharmaceutical / biotechnology / validation documentation / project management / continuous improvement

"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.