안녕하세요?

San Diego, CA 에 위치한 한국 대기업 자회사에서 Projcet Coordinator를 채용합니다.

저희 회사는 In-Vitro Diagnostic Products, Point-of-Care Devices 를 개발/제조/판매 하고 있으며, Chemistry/Biochemistry/Immunology 등의 전공자로써 한국어 기본정도 구사 하실 수 있는 분을 채용코자 합니다.

Salary 및 Benefits 은 San Diego에 위치한 동종 업계 회사들의 평균 수준 입니다.

상세 업무 내용은 아래 참조하시기 바랍니다.

관심 있으신 분들은 danjiyap@gmail.com 으로 이력서 전송 부탁 드립니다.
(다량의 광고메일 또는 도용방지를 위하여 임시 메일 계정 사용하는 것 양해 바랍니다.)

감사합니다.

Required Education, Experience and Skills:

Bachelor or Master Degree in a scientific discipline (chemistry, biochemistry, immunology or related field) combined with minimal or no research or industrial work experience. Knowledge of current MS Office PowerPoint, Project, Word, Excel, and other relevant programs. Above average planning, organizational and communication skills. Ability to learn in-vitro diagnostics requirements and specifics of diagnostic products, point-of-care devices and instrumentation, and industry standards and practices. Adequate comprehension of immunochemistry and quantitative bioanalytical techniques. Understanding of experimental design and basic skills in statistics. Self-motivation, reasonable independence, critical thinking and ability to work on multiple projects simultaneously. Bilingual in both English and Korean is a plus.

Essential Functions/Major Responsibilities:

• Understand product development requirements and prepare practical timetables for achieving projects goals.
• Monitor projects development and maintain respective schedules.
• Organize update meetings, prepare agendas and minutes, and disseminate to group members.
• Work effectively with members of product development (PD), quality assurance (QA), quality control (QC) and manufacturing departments.
• Efficiently manage own time to complete work by specified completion dates.
• Perform other assignments or projects as directed.
• Responsible for compliance with the company’s quality system requirements through training and adherence to policies, procedures and processes.
• Write reports and all necessary documents.
• Support documentation transfer to QA, QC and manufacturing as required.