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.
Requirements:
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.
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.
