Quality Operations Specialist (shift)
RK9595
3 months with possibility of extenison
Greece


We’re currently recruiting for an exciting opportunity with an Pharmaceutical organization based in Greece.

Responsibilities:

• Provide comprehensive oversight of manufacturing of sterile injectables, tablets, capsules and emulsions. Including filling line setup, operation, line clearance, and cleaning processes.
• Ensure all manufacturing operations adhere to standardized protocols for efficiency and compliance.
• Conduct routine inspections and batch record reviews to verify compliance with regulatory standards.
• Lead the investigation of deviations, implementing corrective and preventive actions (CAPAs) to ensure timely resolution, mitigate risks and prevent recurrence.
• Implement change controls, ensuring seamless integration of changes with minimal impact on production.
• Conduct training sessions for manufacturing staff to reinforce best practices, compliance, and efficiency in operations.
• Collaborate with a team committed to efficiency and teamwork, contributing to reduced downtime, increased throughput, and the maintenance of high-quality standards.

• Minimum of 3-5 years of experience in the pharmaceutical industry, with a focus on manufacturing operations, particularly sterile manufacturing.
• Expert knowledge of cGMP requirements and production operations experience.
• Fluent in English, with strong communication skills to effectively lead teams and convey critical information.
• Demonstrated ability to oversee complex manufacturing processes, from setup and cleaning to changeover and compliance checks.