Social network you want to login/join with: Quality Assurance Manager, Nicosia, Sicily Client: GRS Recruitment Location: Nicosia, Sicily Job Category: Other EU work permit required: Yes Job Reference: 5753a8c35ead Job Views: 5 Posted: 14.06.2025 Expiry Date: 29.07.2025 Job Description: A leading pharmaceutical company with global activities is working in partnership with GRS Recruitment to hire a Quality Assurance Manager to join their Nicosia based team. The successful candidate must have extensive working experience in a similar role within the pharmaceutical industry. If you are looking for the next step in your career, GRS looks forward to receiving your CV for this Nicosia-based Quality Assurance Manager role. Main Duties and Responsibilities Ensure the company’s Quality system is in line with current cGMP requirements and relevant legislation. Implement and maintain the company’s documentation system according to cGMP. Oversee production, warehousing, quality assurance, and quality control activities to ensure compliance with cGMP. Update the quality system with new guidelines and EU directives. Draft and maintain high-level documents such as the Site Master File, Validation Master Plan, and SOP list. Participate in management reviews and advocate continual improvement. Ensure effective communication and escalation of quality issues. Define responsibilities related to Pharmacovigilance and perform internal audits in this area. Conduct Product Quality Reviews. Monitor QA key indicators, deviations, change controls, and approve corrective actions. Supervise GMP/QC-GLP assessments in production and warehouse areas. Train personnel on GMP/QC-GLP concepts and review training needs. Participate in internal audits and prepare relevant documentation. Qualify and audit suppliers and contract laboratories, and prepare audit reports. Participate in audits by authorities and customers. Manage corrective action plans and related documentation post-audit. Ensure qualification of GMP-related vendors. Candidate Profile At least 10 years of experience in a similar pharmaceutical QA role. Extensive knowledge of quality guidelines (ICH, WHO, etc.). Strong understanding of EU-cGMP Quality Systems. Fluent in English, written and verbal. Qualified Person registration in Cyprus or another EU country is an advantage. Company Benefits 13th salary Provident fund Flexible working hours Due to high application volume, only shortlisted candidates will be contacted. J-18808-Ljbffr