QC Connectivity Compliance Specialist

Looking for your next challenge where QC validation, equipment connectivity, and regulatory excellence come together?

R&D Partners is seeking a QC Connectivity Compliance Specialist to join a leading pharmaceutical company in Ireland. This contract role focuses on quality control validation and equipment maintenance, specifically related to QC bench equipment connectivity and compliance systems.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

Qualification & Validation Activities:

• Review and approve validation documentation (protocols, reports, risk assessments, traceability matrices) within defined timelines.
• Coordinate the development of validation quality documents to ensure regulatory compliance.
• Document and manage deviations, non-conformances, and corrective actions with proper evaluation.
• Raise and coordinate Change Control Requests (CCRs) for project work, ensuring proper documentation and regulatory impact assessment.
• Ensure compliance with FDA, EMA, and company quality standards across all validation activities.

Collaboration & Continuous Improvement:

• Collaborate with cross-functional teams, including engineering, IT, and external suppliers, for seamless validation execution.
• Identify process improvement opportunities in qualification and validation procedures.
• Contribute to continuous improvement initiatives within the QC connectivity compliance framework.
• Support project management of multiple validation projects simultaneously.

Key Skills and Requirements:

Technical Experience:

• 2-3 years of industry experience in QC validation and quality systems.
• Hands-on experience in Quality Control operations and laboratory environments.
• Knowledge of QC bench equipment and connectivity systems.

Regulatory & Documentation Skills:

• Strong knowledge of FDA and EMA guidelines related to validation and qualification.
• Proficiency in preparing validation documentation, including protocols, reports, and compliance records.
• Experience with change control processes, deviation management, and risk assessment methodologies.

Project Management & Communication:

• Ability to manage multiple validation projects simultaneously while meeting deadlines and budget constraints.
• Excellent communication skills for effective cross-functional collaboration.
• Strong problem-solving abilities for troubleshooting and process improvement.

Preferred Qualifications:

• Experience with connectivity compliance systems in pharmaceutical manufacturing.
• Knowledge of computerized systems validation (CSV) principles.
• Familiarity with calibration management and metrology practices.
• Experience working with external suppliers and contractors.

For more information, please contact Mandi Cakwe.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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