Total 2 job vacancies by Eurofins

Job Responsibilities

• Plan, execute and report audits according to the audit timetable and applicable procedures for the organization, subcontractors, suppliers, and other Eurofins Central Laboratory contacts.
• Plan and execute protocol, laboratory and supporting data, and final report (interim, draft, final) audits and conduct in-life phase inspections as required for compliance with internal SOPs and bioanalytical method validation guidelines (FDA, EMA).
• Perform review of raw data against the draft reports of bioanalytical studies to verify that the reports accurately and completely reflect the raw data generated.
• Perform in life and operational spot inspections- generation of associated reports.
• Monitor the progress, appropriateness and correct implementation of corrective measures.
• Prepare, review and improve QA procedures.
• Review procedures of other departments within the organization.
• Provide quality-enhance training on your own initiative, annual compliance training, and on request.
• Act as a contact person for quality questions from the organization.
• Audit preparation, hosting of client audits and/or regulatory inspections
• Review and evaluate adequacy of investigations and CAPA (corrective actions/preventive actions) reports.
• Maintain current knowledge of standard requirements according to GCLP, GCP, GMP, CAP, ISO17025 and ISO 15189 guidelines related to the business process.
• Archive and document control duties as assigned by QA Manager.
• Perform other related tasks that match training and experience on request of the QA Manager.

Job Requirements

• Bachelor degree in Life Science or a Quality oriented education OR
• MLO education with HLO work and think level
• At least 2 years’ relevant work experience
• Experience with or strong affinity with quality systems set up according to GCLP and/or GCP
• Work experience in the field of ISO / IEC 17025 and 15189
• Confident to engage in the discussion with the management
• Excellent command of English, spoken and written
• Able to increase the quality consciousness of employees
• Strong analytical skills
• Result oriented, sets him/herself concrete targets and does everything to achieve them, taking into account the common interest
• Continuously focused on improvement and optimization of technology and the work process
• Organizational talent, continue to perform effectively under pressure and know how to monitor progress

1. Hỗ trợ chuẩn bị hồ sơ phục vụ công nhận phòng thí nghiệm (VILAS):

+ Tham gia giám sát quy trình phân tích để đảm bảo tuân thủ tiêu chuẩn chất lượng theo ISO/IEC 17025

+ Sắp xếp và hoàn thiện các hồ sơ về thủ tục nhân sự (mô tả công việc, hoàn thành hồ sơ đánh giá tay nghề theo thông tin của bộ phận kỹ thuật)

+ Sắp xếp các hồ sơ về thiết bị (hiệu chuẩn, bảo trì, kiểm tra định kỳ), hỗ trợ in tem, nhãn thiết bị

+ Hỗ trợ tổng hợp các hướng dẫn thử nghiệm và hồ sơ phê duyệt phương pháp

+ Sắp xếp các hồ sơ theo dõi điều kiện tiện nghi môi trường

+ Hỗ trợ trưởng nhóm chất lượng theo dõi và thu thập các hồ sơ theo kế hoạch nhân sự, kế hoạch thiết bị, kế hoạch đảm bảo chất lượng

2. Hỗ trợ các công việc khác theo phân công của phụ trách

Địa điểm làm việc: Khu công nghiệp VSIP Bắc Ninh, phường Từ Sơn, Bắc Ninh (có hỗ trợ chỗ ở miễn phí)