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3-4年经验 -
本科 -
招1人 -
11-09 发布
职位描述
职位描述： Principal Duties and Responsibilities/主要职责（包括但不限于）?Assist in the establishment a Corporate Supplier Compliance program for the evaluation of internal standards and controls for on-going monitoring of Supplier Quality, Document Control, Engineering and Validation, Manufacturing, Technical Quality, and all cGMP related functions within CMAB.?Ensure that the internal audit lit and schedule are maintained and executed as approved.?As lead auditor, perform audits of internal operational departments and associated systems to ensure compliance and adherence to approved CMAB policies and procedures.?Train and develop staff to assist in and/or lead internal audits.?Participate in the execution of the internal auditing program to evaluate the compliance of cGMP operations for CMAB.?The program shall be inclusive of all functional operation groups including but not limited to Engineering & Facilities, Logistics, Manufacturing, Procurement, Quality Assurance, and Quality Control.?Take a lead role in the GMP training function for the Suzhou site, assuring that the training meets CMAB policy and GMP regulations.?Determine GMP training requirements and curricula. Design and conduct, or outsource, training courses to enhance GMP knowledge level among company personnel.?Develop and execute training modules for new hires.?Participate as an active and accountable member in the Product Complaint system and assist with product return, withdrawal or recall activities, as needed.?Assist QA management in hosting regulatory or due diligence inspections. Providing timely response and follow-up to any assigned observations.?Participate in the management of CMAB’s deviation, investigation and CAPA systems.?Provide oversight to CMAB’s Change Management program.Job Requirements/工作经验?BS degree, scientific discipline preferred.?Minimum 4 years experience in QA for a regulated industry, pharmaceutical or medical device experience preferred.？Minimum 3 years in auditing function.？Preferred 1-2 years Supervising in a Quality Systems function.?In Depth knowledge of Biopharmaceutical Manufacturing Operations operating under the control of Good Manufacturing Practices including PIC/S and US-FDA with focus on biological API and sterile product manufacture.？Thorough, in-depth knowledge of Global GMPs and Heath Authority guidelines.?Solid understanding of mAb development, manufacturing, and analytical process.?Advanced level of English – reading, writing, speaking/comprehension & Native Mandarin.?Excellent communication skills in Chinese and English to engage with personnel from multiple disciplines and experience bases across the organization and client base.?Exposure to company and facility start-up.?Strong prioritization and organization skills.?Detail oriented, flexible, self-initiative.?Advanced computer system and database skills – Excel, Word, Power Point, Outlook, etc. 职能类别： 药品生产/质量管理
联系方式
东平街188号
公司信息
苏桥医药（苏州）有限公司是一家致力于抗体及融合蛋白类生物药物的研发、工艺开发、及中试生产的高科技企业，服务范围全面覆盖临床前研究、临床研究、及商业化生产阶段。总投资额为4,640万美元。 苏桥医药是苏州生物纳米科技园（BioBay）重点扶持的企业之一。苏桥在园区内的建造面积共占地7,000平方米，目标产能1期实现69批次，2期实现92批次。 苏桥将严格遵守国际主流药品监管机构的质量标准，包括CFDA、USA (21-CFR) 、EMA (Eurdralex)、PIC/S以及 WHO。苏桥交付的生产样品能够满足客户在全球多个国家临床试验申请的CMC要求。
