上海招聘

Main tasks (primary responsibilities) of the position:
-Accordance with the GMP requirements to guide and supervise relevant departments to improve GMP management.
-Establish, improve and maintain good quality assurance system.
-Organize QA related research, responsible for analyzing & dealing with quality abnormalities in process.
-Translate & improve the technology of new product.
-Design and implement efficient Quality Assurance Standards.

Position requirements, qualifications and experiences:
-Bachelor or above, major in a molecular biology, proficient in professional knowledge and technology in molecular field.
-Preferably working experience in large multinational companies.
-Preferably more than 5 years working experience in QA management.
-Familiar with the pharmaceutical industry, medical equipment and other related laws, master quality, professional R&D knowledge, be able to discover and solve related quality problems timely and effectively.
-Preferably with experience in conducting book/site audit (government, regulatory) and some public relationship management with regulatory agencies.
-Have strong data & logic analysis ability.
-Skillful communication and presentation ability.
-Fluency in English and Mandarin, Proficient in English.

        迈杰转化医学研究（苏州）有限公司，原名凯杰（苏州）转化医学研究有限公司，是一家为精准医疗提供生物标志物的开发、分子诊断产品的研发，以及临床检测服务等一套完整解决方案的创新技术公司。公司团队骨干主要来自跨国药企和诊断公司，有丰富的临床和产品项目经验。
        迈杰旨在凭借行业领先的分子检测技术和专业的客户服务，和临床合作单位共同完成转化医学研究项目，帮助药企伙伴加快药物研发进程和临床试验病人分型入组，并形成伴随诊断试剂盒产品。