崗位職責:
? 根據(jù)生產(chǎn)計劃,制定現(xiàn)場QA工作的日常安排和管理;
? 負責關鍵工藝運行情況和關鍵生產(chǎn)過程參數(shù)(CPPs)的驗證;
? 根據(jù)不同劑型的生產(chǎn)過程,規(guī)范化現(xiàn)場QA工作流程和操作步驟;
? 制定設施、廠房、公用設施和倉庫的審核計劃,并審查其實施情況;
? 制定現(xiàn)場質量控制相關的SOP;
? 定期對現(xiàn)場質量控制人員進行培訓和評估;
? 為生產(chǎn)人員在執(zhí)行偏差、變更和CAPA過程中提供支持;
? 負責生產(chǎn)記錄的審核;
? 協(xié)助進行產(chǎn)品質量審核;
? 領導交辦的其他工作。
? According to the production schedule of each process, arrange the schedule of production QA periodically.
? Verify the operation of critical processes and the critical process parameters (CPPs)
? Standardize the workflow and operation steps of on-site QA according to each process of different dosage form.
? Prepare facility, premises, utilities and warehouse inspection plan and review the implementation.
? Prepare related SOP for on-site QA.
? Training and assessment on-site QA periodically
? Provide support for production personnel in the execution of deviation, change control and CAPA
? Review batch processing records.
? Assist in product quality review.
? Other assignment of QA Manager.
任職要求:
? 本科以上學歷,藥學/理學/應用科學相關專業(yè);
? 3年以上QA部門經(jīng)驗;
? 熟悉口服固體、口服液和乳膏劑型;
? 熟悉PIC/S或者GMP要求;
? 英語書面精通,口語能進行常規(guī)交流,會講普通話或廣東話;
? 熟悉EXCEL、word、PPT等辦公軟件。
? Bachelors degree or above in Science / Applied Science/ Pharmaceutical Study or equivalent.
? Above 3 years work experience in QA department.
? Familiar with oral solid, oral liquid and cream dosage forms.
? Familiar with PIC/S GMP requirement.
? Fluent in spoken and written English, Cantonese or Putonghua.
? Goods computer skill in words, power points, excels.