Job Description

Responsibilities: 1. Demonstrate strong leadership and management skills, communicate effectively, manage multiple workloads and coordinate all QC activities in the physicochemical laboratory with the QC Manager. 2. Participate in development and installation of a KPI system in the physicochemical laboratory assisting to QC Manager 3. Manage and schedule routine and annual maintenance, troubleshooting and of all analytical equipment and analytical practices and procedures in order to uphold continuous improvement in the physicochemical laboratory. 4. Manage Analyst work schedules and ensure that planned work is effectively communicated and adhered to in the physicochemical laboratory. 5. Manage Analyst timesheets, holiday and coordinate all laboratory events and manage laboratory audits and findings in the physicochemical laboratory. 6. Manage Analyst training curriculum and maintain and update all laboratory and analytical documentations in the physicochemical laboratory. 7. Manage and maintain all laboratory software in the physicochemical laboratory. 8. Troubleshoot all QC analytical methods, equipment and calibrations in the physicochemical laboratory. 9. Support continuous improvement in the laboratory and identify gaps in the current QC processes related to physicochemical laboratory and plan improvement/ implementation with the QC Manager. 10. Ensure all testing and associated activities are performed in accordance with GMP and strict industry compliance standards. 11. Manage the QC laboratory waste program in the physicochemical laboratory and ensure that all QC generated waste are properly segregated and disposed. 12. Manage all laboratory OOS, OOT, deviations and change controls in the physicochemical laboratory and liaise with QA etc. 13. Be responsible for equipment qualification, calibration and maintenance in the physicochemical laboratory 14. Be responsible for all method validations in the physicochemical laboratory 15. Provide assistance to QC Manager related to Technical Agreements in the scope of QC Laboratory 16. Provide support to QC Manager in the scope of realisation of the stability studies program of the company 17. Be familiar with Eudralex Vol IV and other related directives and regulations especially those related to QC work. 18. Manage sampling plans and retained sample management 19. Organize, manage and execute chemical and physical testing/ batch analysis 20. Out of Specification (OOS) result investigations and trending 21. Participate in approval of in-process controls 22. Calibration verification of QC equipment in the physicochemical laboratory 23. Responsible for the management of reference standards 24. Responsible for the qualification of QC equipment in the physicochemical laboratory 25. Participate in complaints analysis 26. Organize, manage and execute testing of validation samples in the physicochemical laboratory 27. Contribution to raw material supplier approval for physicochemical laboratory 28. On request of QC Manager provide Assistance in audits of contract labs 29. Participate in Quality Agreement evaluation 30. Participate in Annual Product Review (APR) data compilation 31. Continually assure Pharmacopoeia reviews related to the physicochemical laboratory 32. Participate and manage Statistical Process Control (SPC) / Statistical Quality Control (SQC) 33. Participate in the Environmental monitoring 34. Participate in the global specification standardization 35. On request of the QC Manager, to participate in the Analytical Development either as part of QC or as a separate organizational unit (e.g. method development, method validation, specification generation, method transfer, new QC technologies Pharmacopoeia review, troubleshooting) 36. Participate in analytical method transfers in the physicochemical laboratory 37. Participate in supplier or vendor audits, qualification related to QC activities in the physicochemical laboratory 38. The authorization of written procedures and other documents, including amendments related to QC testing in the physicochemical laboratory 39. QC physicochemical laboratory premises hygiene. 40. Responsible for the retention of relevant records in the physicochemical laboratory. 41. Responsible for the monitoring of compliance with the requirements of Good Manufacturing Practice in the physicochemical laboratory 42. Ensuring that a timely and effective communication and escalation process exists to raise quality issues to the appropriate levels of management 43. Any other duties assigned by the QC Manager related to the pharmaceutical industry