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藥物穩定性研究項目經理 Stability Manager
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職位描述
Responsible for managing and coordinating stability activities of Active Pharmaceutical Ingredient (API) and drug products in cGMP environment. The activities include coordinating sample submission, monitoring stability chambers and preparing documentations such as protocols and reports. The candidate will also be responsible for interacting with all LAB clients, sample receipt, method transfer, project initiation, sample analysis, and providing stability interim reports to our clients. Will manage and coordinate all stability programs. Communicate with LAB clients to design and prepare stability protocols. Collaborate with Customer Services, Quality Control; Quality Assurance; Research and Development functions to ensure all stability programs are being initiated and conducted according to approved protocols. Will monitor all stability programs. Will work closely with Business Development to provide support to LAB clients. Perform statistical analysis and trending of stability data. Coordinate qualification and validation of stability chambers, software and equipment used for stability programs. Supervise stability personnel. Write new SOPs and Implement training programs for staff. Responsible for initiating OOS investigations when required. Provide technical support in the maintenance of lab systems and instrumentation. Ensure that all jobs are completed on time. Responsible for significantly contributing to the conceptualization and development of new procedures, systems, and techniques. Must have extensive experience in managing various stability programs with strong understanding and knowledge of ICH guidelines and FDA stability requirements. This job also requires attention to details and strong time management skills. Must demonstrate skills and past experience in managing multiple projects/programs and/or handles multi-disciplinary aspects of projects. Must be familiar with interpretation of stability data and projecting use-time and expiration date. Exceptional communication and leadership skills and the ability to work effectively in multi-disciplinary team environment are must prerequisite for this position. Experience with various modes of HPLC, pharmaceutical analysis, analytical method development and validation for small molecules as well as proteins and peptides is highly desirable. Must have a winning attitude and business mindset demonstrated by a "can do" approach to issues, resilience, commitment to goals, and persistence. Work with departmental leadership to meet project goals of planning, organizing and delivering effective, on-time. Requires a MS degree (Prefer Ph.D.) in Pharmaceutical Chemistry, or in equivalent scientific field with a minimum of 5 years of relevant experience. Previous stability department supervisory experience is required. Must demonstrate proficiency with the preparation of regulatory submissions, ability to manage multiple projects and meet critical deadlines. Must demonstrate successful interdisciplinary collaboration in a team setting. Communicate (verbal and written) information in a timely manner to clients and department supervisor. Demonstrated successful interdisciplinary collaboration in a team setting. This position requires the ability to manage the stability department. 工作職責:1.負責管理和協調穩定的活性藥物成分和cGMP的藥物產品環境。 2.負責所有客戶的實驗室,進行分析,提供穩定的中期報告。 3.管理和協調所有穩定性程序。4.編寫新的SOP和實施員工培訓計劃。5.在實驗室系統和儀表維修提供技術性支持。 任職資格:藥物化學碩士(博士優先)。5年以上的相關工作經驗。 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.
企業簡介
杭州艾品醫藥科技有限公司由浙江工業大學獨資創立,憑借與美國IPS公司的全面合作及長三角綠色制藥協同創新中心提供的全方位支持,專注于為意在出口制劑、原料藥等產品到歐美市場的在華醫藥生產企業提供符合美國FDA認可的全面藥品質量檢測及其它相關服務。 長三角綠色制藥協同創新中心是教育部、財政部批準的首批14個“2011協同創新中心”之一,由浙江工業大學牽頭,聯合浙江大學、上海醫藥工業研究院、藥物制劑國家工程研究中心、浙江省醫學科學院、浙江省食品藥品檢驗研究院等作為核心共建單位,由共同致力于提升科技創新能力和拔尖創新人才培養能力、服務和引領制藥產業轉型升級的高等院校、科研院所、企業和國際創新機構等單位聯合組成。
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熱門區域招聘: 重慶 北京 上海 浙江 江蘇 廣東 山東 湖南 安徽 河北
浙江招聘企業: 浙江佐力藥業股份有限公司 河南宛東藥業有限公司 杭州安杰思醫學科技有限公司 浙江中法制藥有限公司 貴州益佰制藥股份有限公司 福成堂大藥房 杭州杏園科技有限公司 杭州諾康醫療器械有限公司 浙江正京元大藥房連鎖有限公司 杭州明興生物科技有限公司
職位發布日期: 2015-01-16