QA Specialist - Greece

We’re currently recruiting for an exciting remediation with a pharmaceutical organization based in Greece. This is an excellent opportunity to make a tangible impact in a short space of time.

Duties

• Oversee the setup, operation, line clearance, and cleaning of the OSD filling line, ensuring all processes are conducted effectively.
• Ensure all manufacturing activities comply with established protocols to maintain operational efficiency and regulatory compliance.
• Perform regular inspections and review batch records to confirm adherence to regulatory requirements.
• Lead investigations into process deviations and implement corrective and preventive actions (CAPAs) to resolve issues promptly, reduce risks, and prevent recurrence.
• Manage change control processes to ensure smooth implementation of changes with minimal disruption to production.
• Deliver training to manufacturing staff to promote best practices, compliance, and operational efficiency.
• Work closely with a team dedicated to efficiency and collaboration, contributing to reduced downtime, increased throughput, and the maintenance of high-quality standards.

• At least 5 years of experience in the pharmaceutical industry, specializing in manufacturing operations, with a focus on OSD production.
• Extensive knowledge of cGMP requirements and hands-on experience in production operations.
• Proficient in English with excellent communication skills, enabling effective team leadership and clear communication of essential information.
• Proven track record of managing complex manufacturing processes, including setup, cleaning, changeover, and compliance verification.