工作內容：
1.法規的符合性Compliance with regulations
1.1.學習國家藥品法律、法規，以指導質量管理工作，保障GMP生產部門的各項工作符合國家相關法規。
Learn national drug laws and regulations to guide quality management and ensure that the work of GMP production department complies with relevant national laws and regulations.
2.廠房、設施、設備Buildings、Facilities、Equipment
2.1.負責GMP廠房、設施設備及其相關記錄的日常檢查和管理工作，保證其可以正常運行并且滿足GMP生產需求。
Responsible for the daily inspection and management of GMP factories, facilities, equipment, and related records to ensure their normal operation and meet GMP production requirements.
2.2.監督純化水系統的管理，負責對工藝用水的生產進行檢查，審核相關記錄。
Supervise the management of the purified water system, responsible for inspecting the production of process water and reviewing relevant records.
2.3.監督潔凈區空調系統的管理，負責潔凈區環境監控的跟蹤和相關記錄的審核。
Supervise the management of HVAC. Responsible for monitoring the clean area environment and auditing the related records.
2.4.負責害蟲控制執行的監督和記錄的審核。
Responsible for supervising the implementation of pest control and reviewing the record regularly.
3. 計量器具管理Management of the Measuring Instrument
3.1.負責監督計量器具依據國家法規和相關SOP完成計量器具的年度校準計劃，計量器具分類評估。
Responsible for supervising the completion of the annual calibration plan and classification evaluation of measuring instruments in accordance with national regulations and relevant SOPs.
3.2.確保儀器儀表的定期校準工作，簽發計量合格標簽，確保校準證書在有效期內，將計量證書歸檔保存。
Ensure periodic calibration of instruments and meters, Issue metrological labels,Ensure the calibration certificate is valid, Certificate of metrological filing.
4.驗證管理Validaiton Management
4.1.審核GMP年度驗證總計劃，監督生產部門驗證計劃執行情況。
Review the GMP annual validation master plan and supervise the implementation of the validation plan by the production department.
4.2.參與GMP制劑生產部門驗證方案、記錄和驗證報告的審核，在驗證完成后進行歸檔保存。
Participate in the review of GMP DP production department validation plans, records, and validation reports, and archive and preserve them after the validation is completed.
4.3.監督檢查在驗證實施中的偏差及整改措施。
Supervise and check the implementation of the deviation and corrective measures in validation.
5.物料及供應商管理Material management
5.1. 負責供應商審計工作，收集供應商資質資料、問卷，起草審計報告，維護供應商清單，確保物料的供應商均經過審計和批準。
Responsible for supplier audit, collecting the supplier qualification material, questionnaire, preparing the supplier audit report, maintaining the supplier list,ensure material suppliers are audited and approved.
5.2. 監督物料的入庫、儲存和出庫管理，審核物料管理記錄并完成物料的放行, 監督不合格物料管理以及特殊物料管理。
Supervise material entry, storage and exit management, review material management records and complete material release, supervise nonconforming material management and special material management.
5.3. 發放物料代碼
Issue the material code.
6. 制劑產品臨床標簽Clinical Labeling of DP
6.1. 負責標簽模板的審核批準，簽署 臨床標簽模板審批表，確保標簽內容符合國家法規及相關SOP的要求。
Responsible for the review and approval of the label template, sign the Review and Approval Form of Clinical Label Template, and ensure that the label content conforms to the national regulations and related SOP requirements.
6.2. 負責臨床產品標簽的訂購/打印及檢查放行。
Responsible for clinical product label ordering/printing and inspection release.
6.3. 負責QA條碼打印機的使用、清潔維護管理。
Responsible for the use, cleaning, maintenance and management of QA barcode printers .
7. 項目管理Project Management
7.1. 審核生產前的主批生產記錄及生產后執行批記錄。
Review the master batch records and the execution batch records.
7.2. 負責監督產品從物料進入生產工藝之后的生產、包裝和發貨的全過程。
Responsible for supervising the whole process of production, packaging and delivery of products from the raw material into the production process.
7.3. 負責生產過程中的清場放行檢查，物料取樣后的清場放行檢查。
Responsible for clearance release inspection during production process and clearance release inspection after material sampling
7.4. 負責項目清潔確認的審核批準，配合相關部門進行清潔確認工作, 放行已清潔合格的設備。
Responsible for the reviewing and approval of the project cleaning verification, and cooperate with relevant departments for cleaning verification, release clean and qualified equipment.
8. 負責監督制劑生產部門使用記錄的發放和回收。
Responsible for supervising the release and recovery of the use records of the DP production department.
9. 參與工作相關的偏差、變更控制、投訴等質量事件的調查。
Participate in the investigation of work-related deviations, change control, complaints and other quality incidents.
10. 參與GMP制劑車間、設備間及庫房的日常巡檢工作。
Participate in the routine inspection of GMP DP workshop, equipment room and warehouse.
11. 完成本部門領導臨時安排的工作。
Complete other tasks arrangements by department head.
教育背景及任職資格
1.教育背景：化學、應用化學、藥學或相關專業本科或大專及以上學歷
Education Background：Bachelor degree or college degree above in chemistry, applied chemistry, pharmacy or other related fields.
2.經驗：應當至少具有藥學或相關專業本科或大專學歷（或中級專業技術職稱或執業藥師資格）。本科學歷，具有至少1年從事藥品生產和質量管理的實踐經驗，接受過與所生產產品相關的專業知識培訓。大專學歷（或中級專業技術職稱或執業藥師資格），具有至少2年從事藥品生產和質量管理的實踐經驗，接受過與所生產產品相關的專業知識培訓。
Experience: A bachelor degree or college degree above in pharmacy other related field(or qualified midlevel with the title in professional or licensed pharmacist ), bachelor degree ,more than 1 years of experience in drug production and quality management, trained in professional knowledge related to the products produce. college degree (or qualified midlevel with the title in professional or licensed pharmacist ), more than 2 years of experience in drug production and quality management, trained in professional knowledge related to the products produce.
3 技能技巧：具有一定的專業英語讀寫能力。
Skills: have a certain ability to read and write in professional English.