職位描述
The Compliance Manager is responsible for Compliance functions to include: document control, regulatory compliance, internal audits, client audits, change control, complaints and personnel training records. This position requires the ability to manage and supervise employees and have good problem solving abilities. Must be able to interface effectively with internal personnel, clients, and auditors, including the FDA; prepare proper response to any observation as required on timely manner. This position is also responsible for all laboratory safety issues to include: safety training, safety audits of the laboratory, and disposal of chemical waste. Excellent communication (verbal & written) and customer services skills required. Excellent writing skills and experience writing technical documentation & reports required. Ability to simultaneously manage multiple tasks/priorities. Excellent problem solving skills/abilities. Good time management and negotiating skills required. Capacity for independent work required. Demonstrated ability to manage multiple projects and meet critical deadlines. Demonstrated ability to work in a team-oriented environment. Must have strong knowledge and experience in dealing with compliance issues in a pharmaceutical analytical laboratories. Will be required to assist with the preparation, execution, documentation, status updates and review of training sessions on a variety of department and regulatory topics. Other related duties as assigned. Must have good time management skills and able to perform to deadlines. Ensure that project milestones are met and documented. Ability to manage simultaneous tasks, work under pressure, track and monitor progress of multiple projects and follow through to goals. This position requires the ability to manage and supervise employees and have good problem solving abilities. Requires excellent troubleshooting ability, communication skills and ability to present data to clients and regulatory agencies. Requires a M.S. Degree in Science with at least 5+ years regulated documentation experience in the pharmaceutical industry. Experience in the contract testing laboratory industry preferred. 合規經理負責合規功能包括:文檔管理、遵守規章制度、內部審核、客戶審核,變化控制、投訴和人員培訓記錄。這個職位需要的能力和督導員工的能力,有良好的解決問題的能力。必須能夠有效地與內部人員，客戶,和審計,包括FDA進行交流;準備適當的應對任何及時觀測的要求。這個職位還負責所有實驗室安全問題包括:安全培訓,實驗室安全審計和化學廢物的處理。優秀的溝通(口頭和書面)和客戶服務技巧。優秀的寫作技巧和經驗寫技術文檔和報告要求。能夠同時管理多個任務。優秀的解決問題的技能/能力。良好的時間管理和談判技巧。有獨立工作的能力。管理多個項目的能力和滿足關鍵的最后期限。證明了在團隊的環境中工作的能力。必須有很強的知識和經驗在實驗室藥品分析問題上?？梢詤f助準備、執行、文檔、狀態更新和審查培訓班各種部門和監管的主題。其他相關職責分配。必須有良好的時間管理能力,能夠執行期限。確保滿足項目里程碑和記錄。同時任務管理能力,在壓力下工作,跟蹤和監控多個項目和完成目標的進展。這個職位需要的能力管理和督導員工的能力,有良好的解決問題的能力。需要良好的故障診斷能力、溝通技巧和能力展示數據給客戶和監管機構。需要科學碩士學位至少有5 +年制藥行業規范文檔的經驗。合同測試實驗室行業經驗者優先。職位概覽 為配合公司實驗室建設及開展檢測業務，杭州艾品公司特此招聘以下各個部門的各類層次人員 (Technician, Associate, Supervisor, and/or Managers): Analytical Chemistry; Analytical Development; Stability; Biopharma; Microbiology; Quality Assurance; Business Development & Marketing; Finance; Human Resources; MIS; ICVS; Corporate Planning & Scheduling; Purchasing & Facilities;注意：成功應聘者將由杭州艾品公司直接聘用并提供薪酬及福利待遇。所有雇員與長三角綠色制藥協同創新中心或其協同成立單位（包括浙江工業大學）將無任何形式的勞務關系。聯系方式 Contact Info： 人事經理 hr@irvinepharma-china.com 請按照下列格式書寫email主題：申請部門_職位_最高學歷_姓名。舉例，一位叫張三的申請者，最高學歷是碩士（MS），申請分析部門(Analytical Chemistry) 的HPLC Supervisor職位，則主題格式為：Analytical Chemistry_HPLC Supervisor_MS_Zhang San。同時，請按照同樣規則將所附簡歷命名。即其簡歷命名為Analytical Chemistry_HPLC Supervisor_MS_Zhang San.If using email to forward resume, please follow the renaming rules below: Department_Position_Highest degree achieved_Last name First name. For example, an applicant named Zhang San wants to apply for the position of HPLC Supervisor in the department of Analytical Chemistry. The highest degree he had is M.S. Then please write email subject as Analytical Chemistry_HPLC Supervisor_MS_Zhang San. On the other hand, please rename the resume to Analytical Chemistry_HPLC Supervisor_MS_Zhang San as well.
