Supervise and verify the implementation of the Quality and Food Safety Management System in the factory, ensuring compliance with company standards across all production stages.
Responsibilities
Supervise and verify the implementation of the factory Quality and Food Safety System so that the products produced comply with company standards
Monitor the implementation of improvement recommendations for the Quality and Food Safety System
Conduct periodic checks on reports provided by QC analysts for microbiology, incoming material, and in process control and report them to the QC Section Head
Conduct inspections and collect data related to product complaints for follow-up corrective actions
Review the calibration program for quality measuring instruments and supervise its implementation and follow-up of the results obtained
The Quality Manager is responsible for developing, improving, implementing, monitoring and maintaining quality systems and supporting processes to ensure compliance to regulatory requirements for the industries we serve. The Quality Manager will provide technical leadership within the Quality discipline, driving adherence to systems and maintaining high levels of customer focus. The Quality Manager is also responsible leading follow-up corrective action and direction of all customer-related quality issues
Compensation
Discretionary annual bonus program (initial eligibility dependent upon hire date)
Responsibilities
Puts safety first in all responsibilities including awareness and adherence to all corporate and site environmental, health, and safety policies
Be an active member of the plant leadership team
Serve a the “Management Representative” for audits and other related customer and internal quality inquiries
Provide leadership to the quality team
Manage Amcor Plant Quality System and maintain registration to chosen quality standards
Requirements
Bachelor’s Degree in science or engineering or equivalent experience
Nice to have: Lean Manufacturing
Nice to have: Six Sigma
Nice to have: Formal training in problem solving techniques
Manages assigned clinical customer projects to ensure that project goals and objectives are accomplished within the prescribed time frame, budget, and in accordance with customer expectations.
Responsibilities
Accountable for overall project management for assigned projects/customers using appropriate project planning tools
Communicates milestones, critical path activities, and assigns internal and external responsibility to ensure the project achieves all deliverables per the customer requirements and agreed upon timelines
Primary customer contact for clinical packaging and/or distribution activities and relationship management with the customer project teams for assigned projects/customers
Provide support to business development and estimation regarding new quotations and resupplies
Provide continuous support to Project Manager and team by being the daily point contact for day-to-day internal problem solving and trouble-shooting
Requirements
GCSE Grade C and above in English, Science and Mathematics (or equivalent)
A Level/NVQ/HNC or equivalent in Applied/Life Sciences, Mathematics or Business related degree (desirable)
Phụ trách quản lý bảo trì hệ thống Utility tại nhà máy như: compressor, chiller, AHU, electrical station, water treatment,...
Responsibilities
Quản lý bảo trì hệ thống Utility tại nhà máy
Đảm bảo sự tuân thủ mọi nội quy, qui định và kỷ luật của nhà máy và công ty
Tham gia các buổi huấn luyện về an toàn và chuyên môn
Quản lý & bảo đảm tất cả thiết bị tiện ích /dây chuyền mới (hoặc có sự thay đổi thiết bị) phải được đánh giá rủi ro và có biện pháp ngăn ngừa trước khi bàn giao đưa vào sản xuất
Theo dõi, quản lý nhà thầu làm việc tuân thủ những nguyên tắc kiểm soát an toàn trong việc thực hiện công việc của mình
Requirements
Cử nhân Đại học các ngành liên quan bảo trì, sửa chữa, điện-điện tử, cơ điện tử hoặc các ngành liên quan
Qualitätskontrolleur*in im GMP-Umfeld für Rohstoffe, Zwischenstufen und Wirkstoffe.
Responsibilities
Führe Gehalts- und Reinheitsprüfungen an Rohstoffen, Zwischenstufen und Wirkstoffen mit modernsten Analyseverfahren (HPLC, GC, NMR, UV/Vis) präzise durch
Stelle die GMP-gerechte Dokumentation und Auswertung aller Analysen sicher
Übernimm die Probenahme, Verteilung und Verwaltung nach festgelegten Verfahren
Sorge als Geräteverantwortliche*r für die Verfügbarkeit und den einwandfreien Zustand der Laborgeräte
Unterstütze aktiv bei der Erstellung und Prüfung von SOPs und Prüfanweisungen
Requirements
Abgeschlossene Ausbildung als Chemielaborant:in, Chemietechniker:in oder Chemisch-Technische:r Assistent:in oder vergleichbar
Prüfung angelieferter Rohstoffe und hergestellter Endprodukte auf Konformität, Dokumentation von Qualitätsabweichungen und Durchführung von Qualitäts- und Hygienerundgängen.
Responsibilities
Wareneingangskontrolle anhand von Spezifikationen und CoAs
Prüfung hergestellter Produkte auf Konformität und Dokumentation
Bewertung und Dokumentation von Qualitätsabweichungen
Durchführung regelmäßiger Qualitäts- und Hygienerundgänge
Bewertung von Retouren hinsichtlich Zustand und Mängeln
Requirements
Abgeschlossene Berufsausbildung in einem relevanten Bereich
Supplier Development Quality Engineer responsible for activities related to supplier selection and evaluation, material qualification, supplier performance and receiving inspection.
Compensation
The base pay for this position is $78,000.00 – $156,000.00
Responsibilities
Contributes to the development, maintenance and improvement of division supplier development quality program policies, procedures and forms
Provides guidance and training to Purchasing, R&D, Manufacturing and Quality engineers in applying program requirements
Reviews and approves all supplied product drawings and component quality plans
Manages development of supplied product inspection procedures and first article requirements
Provides engineering guidance to division Receiving Inspection including statistical analysis, measurement techniques, Gage R&R studies and inspection procedures
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