Home Job Postings Project Coordinator & Quality Associate Position This topic has replies, 0 voices, and was last updated 3 years ago by Jennie Kang. Now Editing “Project Coordinator & Quality Associate Position” Name * Password * Email Topic Title (Maximum Length 80) Company * Location Expires at 저희 SigmaGraft는 플러튼에 위치한 메디칼 제품 제조 회사이며 아래와 같이 직원을 모집합니다. (홈페이지: www.sigmagraft.com) 관심 있으신 분은info@sigmagraft.com 으로 이력서를 보내 주시기 바랍니다. Contact : Jennie (714)525-0114 ext. 115 Project Coordinator - Full Time We are seeking a Project Coordinator who will be in charge of assisting our General Manager in organizing our ongoing projects and will operate as a point of contact for any and all matters specific to the company's projects. The Project Coordinator is a member of the operations team and will work with the team to ensure timely and successful delivery of projects implementations. The Project Coordinator will also work independently to deliver on responsibilities in collaboration with General Manager and operations team. Tasks involve monitoring project plans, schedules, work hours, budgets, and expenditures, organizing and participating in meetings, and ensuring that project deadlines are met in a timely manner. Other responsibilities and duties for this position include: Required Skills • Developing project strategies. • Ensuring projects adhere to frameworks and all documentation is maintained appropriately for each project. • Evaluate potential problems and technical hitches and develop solutions. • Supervise current projects and coordinate all team members to keep workflow on track. • Create a project management calendar for fulfilling each goal and objective. • Provide updates on projects to senior management team. • Schedule project meetings per project plan and/or need. Education: • Bachelor's preferred • Strong analytical skills • Competent in using Microsoft Office applications such as Word and Excel • Exceptional verbal, written, and presentation skill • Strong record-keeping and organizational skills Quality Associate - Full time Key Responsibilities: · Create and/or revise procedures, guidance and related forms managed by the Quality Department. · Document Control Coordination. · Review of raw material and packaging component in-coming inspections. · Review of new raw material specifications. · Perform review of routine facility inspection conducted by the QC department. · Prepare issuance of Certificate of Conformance certificates issued to customers · Assists in the supplier qualification. · Review of product batch records prior to product release. · Assists in internal investigations from customer complaints, NCR, audit nonconformities and CAPA. · Perform other duties as assigned. Knowledge and Skills: Detail oriented and highly organized. Fast learner, able to multi-task and keep track of commitments and goals. Good time management skills and ability to adopt to changing priorities, as needed. Good analytical skills and good working knowledge of Microsoft Office Applications such as Word, Excel, Powerpoint, Outlook and Adobe Acrobat. A team player, able to work in a team of different ethnic background. Education: Graduate of a college degree (science degree preferred) or equivalent experience working in a GMP laboratory preferably a medical device, pharmaceutical or similar manufacturing environment. *Benefits - Paid Sick Days, Holidays & Vacation, Medical Insurance, 401K - Working hour: 8am to 5pm, Monday ~ Friday I agree to the terms of service Update List
