02 ago
|
Accord Healthcare
|
Italia
02 ago
Accord Healthcare
Italia
ppThe QA Supervisor will have To ensure that current and future EU GMDP requirements are met and that an effective and robust Pharmaceutical Quality System is maintained. /p pProvide direct support in the management/maintenance of the day to day aspects of the QA. To work with other departments to ensure a strong QA culture throughout the business and providing guidance as required. /p h3The Role /h3 ul liEnsuring general EU GMP/GDP compliance as well as compliance to local regulations. /li liLiaising with Corporate office/BRS/Warehouse for batch related documents, including importing documentation, Data Loggers, CMR, etc. /li liReview and evaluate batch release documents for local release with the warehouse. /li liCoordination of BRC/CoA Activities with QA Corporate. /li liSupport managing and reporting Rapid alert activities and GMP non‑compliance alert (AIFA notifications). /li liMaintain local QMS in accordance with Corporate QA requirements. /li liManage Change Controls, Deviations, CAPA and Risk Management. /li liMastering Recalls, returned goods, Market complaints and Medical Enquiries, both at Corporate level and at customers’ level. /li liMaintain in maintenance of ISO 9001 and ISO 14001 certification. /li liQA training: coordinating with all departments and new comers for training and maintaining the training records for GMP/GDP/QMS. Maintain Qedge TMS system for all local trainings. /li liPlanning and conducting Self‑inspections. /li liCoordinate with contract warehouse for PQR preparation, review maintenance related to Repacking activities. /li liSupport to Tender Dept. for qualitative related documentation. /li liMaintenance of RA/QA internal databases and product master data. /li liDTF process and Importation activities due to AIFA shortages and commercial opportunities, including Dossier drafting for AIFA submission (i.e Product Identity Declaration from releasing QP, Import authorization request...). /li liQuality Technical Agreement activities.
/li liEnsure that sampling activities for import batches from non‑EU countries are performed in compliance with internal GMP / SOP from the warehouse. /li liEvaluate and ensure the integrity of import shipments based on the documentation shared by the warehouse. /li liRetrieval of data loggers and collection of temperature excursions for evaluation and approval. /li liSupport on maintenance and renewal of the Narcotics / Narcotics Authorization Decree: ensure that all Narcotics licenses are applied and available for import / export shipments in order to comply with Italian law. /li liSupport for the import process from EU and non‑EU countries, Customs clearance and invoicing process (Direct Shipment). /li liSupport local affiliate in SOP creation, update and management. /li /ul h3The Person /h3 ul liPrevious professional experience on similar position in QA Department in pharmaceutical company or national competent authority could be a plus. /li liKnowledge of general EU GMP and GDP requirements and local laws and requirements such as D. Lgs. 219/2006. /li liExperience of conducting quality based investigations and root cause analysis. /li liUnderstanding and experience of Product Quality Review requirements, Change Control, CAPAs, Deviation management and validation/qualification activities. /li liCommunication skills with a strong focus of collaboration. /li liExcellent knowledge of MS Office, especially Excel. /li liFluent English (B2 is minimum). /li liQualifications: pharmacy, biotechnology, biology, chemistry or similar. /li liCertifications or accreditations: auditor qualification could be a plus. /li /ul h3The Rewards /h3 ul liBase annual salry between 41.000 EUR and 45.000 EUR based on experience and interview outcome. /li liTicket restaurant. /li liAnnual premio. /li liTraining and development. /li liFlexibility. /li /ul pAll applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability. /p /p #J-18808-Ljbffr
📌 Quality Assurance Supervisor (Italia)
🏢 Accord Healthcare
📍 Italia