Mantas Zilinskas

-Set up, operate, and monitor filling machinery and equipment to ensure the accurate and efficient filling of pharmaceutical products, while strictly adhering to Good Manufacturing Practices (GMP) and quality standards.
- Maintain high standards of GMP by following Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and related documentation as directed by the Team Leader.
- Ensure the cleanliness and sanitation of the filling line and equipment by adhering to established cleaning protocols to prevent contamination.
- Collaborate with team members and cross-functional departments to troubleshoot equipment issues and implement effective solutions, enhancing overall operational efficiency.
- Accurately complete production records and batch documentation, ensuring compliance with company regulations and quality assurance standards.
- Perform end-of-batch reconciliation with precision to ensure accuracy and integrity of production data.
- Adhere to safety protocols and regulations to maintain a safe working environment.
- Participate in ongoing training and assist in onboarding new team members, fostering a culture of continuous improvement and development.
- Contribute to process improvement initiatives, resulting in increased production rates and reduced error margins.

• Overseeing or preparing necessary paperwork and reports necessary for completion of work orders; Coordinating with Manufacturing Manager, Quality Assurance Technicians and Engineers to ensure that quality standards are maintained in production
• Overseeing general maintenance of the clean room to insure a healthy work environment for employees and to maintain neatness and order; Supervises production workers and leads by Reviewing work performed and providing feedback regarding performance to achieve monthly targets; Precise and attentive to details and safety; Capable of constant adapting and learning of new processes and equipment; Using SyteLine ERP System to generate Process Record Cards, Set up heat sealers; Checking Fedegari loads for QA release and sterilisation; Autoclave Load Building; Labelling, Pouching and Sealing Standard BSI Lenses; Operation of Transfer Hatches, Air Shower and Airflow cabinets; Transfer to/from Cold-store; Generating IT Tickets; Other tasks required by team leaders;