轉職熱搜工作

SHL Medical is the world-leading solution provider in the design, development, and manufacturing of advanced drug delivery systems with more than 5000 employees worldwide. Our customers include top pharmaceutical and biotech companies from around the globe that require innovative devices such as auto injectors or pen injectors to effectively deliver their drugs. Headquartered in Switzerland, SHL has sites in Sweden, Taiwan, and the Unites States. Job Overview This role is embedded in the Packaging & Forming Technology Team within our Operations Engineering Department in Taiwan. Your responsibilities ● Together with the rest of your team you will support the production of packaging material and component printing processes for our autoinjector systems ● Lead engineering responsibility for packaging production lines and printing processes within our production system ● Collaborate closely with shop floor production technicians, maintenance, quality and process development on performance/process improvements and trouble shooting ● Lead the development of improvement plans and requirements for capacity expansion and future packaging and printing concepts ● Lead improvement initiatives and capacity deployment in packaging and printing ● Responsible for manufacturing acceptance of new packaging and printing processes in regular production ● Support Design For Manufacturing (DFM) and definition of manufacturing requirements for new products We offer - Competitive compensation package - Flexible hours and working from home policy. - Modern working environment with state-of-the-art facilities and technologies - Challenging assignments in a fast growing and innovative industry - Position in a dynamic, international team of highly skilled professionals - Various opportunities for personal and professional development within a global organization

【Job Overview】 This role is embedded in the Automation Technology Group within our Global Operations Engineering team in Taiwan. 【Your responsibilities】 ● Lead and develop a team of experts to support the production in high-speed assembly and packaging of our autoinjector systems ● Understand current practices and develop new or improved assembly processes, automation solutions and automated inspection methodologies based on in-depth processing experience, automation engineering fundamentals and equipment design knowledge. ● Promote use of new technologies and industry-leading trends. Provide highest level of technical expertise ● Lead engineering accountability for automated assembly and test equipment, device assembly and corresponding processes within our production system ● Collaborate closely with Plant / Production manager, automation vendors and maintenance, quality and process development on performance/process improvements and trouble shooting ● Lead the development of improvement plans and requirements for capacity expansion and future equipment generations and production setups ● Lead improvement programs and capacity deployment in device assembly and packaging automation ● Accountable for manufacturing acceptance of new assembly and test equipment in regular production ● Lead Design For Manufacturing (DFM) and definition of manufacturing requirements for new products and product care initiatives ● Organize and lead plant level training activities to improve assembly / automation problem solving capabilities and process efficiencies 【Your qualification】 ● Degree in Mechanical Engineering, Automation or similar education/experience ● Minimum 15 years of relevant industry experience; hands-on experience with high-speed automated assembly of plastic and metal components ● Deep understanding of equipment design, process automation and relevant sub-systems (pneumatic/electric actuators, cam-driven pick and place systems, optical/capacitive/inductive and other sensor technologies, servo-driven systems) ● Experience with commissioning, qualification and validation of large automation equipment and processes ● Thorough understanding and hands-on experience with Siemens and/or Beckhoff PLC based systems, common sensor and actuator system, and vision technologies ● Hands-on experience in programming PLC/IPC and SCADA is highly preferred ● Advanced knowledge of common problem-solving and Root Cause Analysis (RCA) methodologies ● Proven track record in leading and developing a team of highly specialized experts; management experience ● Passionate & committed self-starter with “can do” attitude, team player and taking responsibility to get the job done ● Previous exposure to a highly regulated industry (e.g. medical, pharmaceutical) and knowledge of relevant standards (e.g. ISO13485, cGMP) is a plus ● Intercultural and interdisciplinary communication skills; able to communicate effectively in English (verbal, written) ● Ability to communicate in Mandarin is a plus 【We offer】 ● Competitive compensation package ● Flexible hours and working from home policy. ● Modern working environment with state-of-the-art facilities and technologies ● Challenging assignments in a fast growing and innovative industry ● Position in a dynamic, international team of highly skilled professionals ● Various opportunities for personal and professional development within a global organization

QE team expand in 2023! We‘re lookng for the experienced partner working together! Job Overview The Quality Engineer is responsible for supporting new product development, process development and product care through the application of Quality engineering skills for medical devices. This person will handle projects and tasks, from product/process inception through product launch, scale-up and maintenance and play an active role in the processes to ensure products meet quality standards consistent with Customer Requirement, while meeting all design control and other regulatory requirements, including, but not limited to FDA Quality System Regulation 21 CFR Part 820, ISO 13485, ISO 11608 & ISO 14971 Main Responsibilities • Team member representing Quality on new product/process development and product care projects. • Ensures that all design control and production / process control projects meet applicable regulatory (local and international), Corporate, Customer, and Local QMS requirements. • Assess and approve the risk mitigation techniques implemented and whether these are consistent with the product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls – UFMEA, DFMEA, PFMEA. • Develop quality plans and work further with Manufacturing on the transfer of quality requirements. • Promotes the use of statistics in the testing and control of quality. • Supports Device product/process development and production activities, including the following: - Develops or reviews product/process verifications/validation or test plans (protocols and reports). - Develops or reviews product/process specifications and requirements. - Develops or reviews product reliability specifications/predictions, reliability test activities. - Participates in risk management activities including review failure mode effects analysis (FMEA), hazard analysis, - fault tree analysis (FTA) and/or risk or statistical analysis. - Participates in product or process design and change activities, including design reviews. - Provides technical support for product quality attributes/decisions. - Support selected verification/validation activities (e.g., toxicology/biocompatibility, sterilization validation, etc.)with external suppliers. • Contributes to compilation and maintenance of Design History Files (DHF). • Ensures proper design and development documentation as per ISO 13485/FDA QSR Quality System Required Skills & Qualifications • Education:Technical / scientific degree at college / university level (mechanical, industrial, biomedical, chemical engineering, material/life science) Experience_Occupational experience • At least five years’ work experience in a Product Development/Design Assurance function in regulated environment (medical devices/Diagnostic instrumentation industry, pharmaceutical or biotechnology industry.) • Experience in the design and development of products in accordance with ISO 13485 guidelines. • In depth know-how and experience of quality techniques: Six Sigma Blackbelt, Six Sigma methods such as DFSS, DMAIC, DoE, FMEA, etc. • Experience in modular automation/fully automated assembly processes, particularly those involving plastic injection molded parts, mechanical spring, with integrated/non-integrated testings • Experience in the entire Design life-cycle and Phase-Gate development process. Experience_Special knowledge, expertise, experience • cGxP Know-How incl. regulations ISO 13485, FDA 21 CFR 820, MDD 93/42/EEC • Statistical methods • SAP (Manufacturing Execution Systems / MES will be an advantage) • English (spoken and written), local language (Mandarin) is a plus

【Job Overview】 This role is embedded in the Factory Development & Projects Group within our Global Operations Engineering team in Taiwan. 【Your responsibilities】 ● Lead the development and implementation of factory and plant layouts together with our internal planning and SME teams and external contractors (architecture, design, planning, etc.) ● Ensure all stakeholder requirements are considered in the planning process and are translated into optimized factory designs, both from an Operational and Sustainability standpoint ● Review factory design and optimize site layouts for production, material flow, construction, and facilities. ● Convert identified potentials in production and logistics processes into a competent planning. ● Ensure compliance with relevant Codes, Standards and HSE requirements ● Ensure execution of standards, processes and procedures for effective delivery of operations excellence ● Work with manufacturing, logistics, facilities teams and contractors to ensure that equipment and layout designs align with the overall logistics and operational plans of for the factory ● Factory equipment and facilities: Develop equipment specifications and requirements based on product constraints / Provide design layouts and equipment solutions / Conduct equipment design reviews and provide design guidance to vendors. ● Support integration of systems and processes in to global digital landscape (EWM, EAM, MES,…) ● Provide technical leadership support to Project Managers to drive planning, implementation and project execution with the team ● Review and approval of critical layouts and facility specifications (space allocation, material flow, MEP, etc.) 【Your qualification】 ● Degree in Engineering, Construction, Production Management or other relevant discipline ● Minimum 10 years of relevant industry experience in Production Management, Operations/Logistics or Factory Planning/Design ● Hands-on production/logistics management experience in a high-volume, high-throughput production environment; Familiar with LEAN process optimization ● Proficient in layout design (preferably AutoCAD) and relevant drawing standards ● Knowledge of automated material handling / warehouse systems, production logistics, end of line installations, warehouse transportation and material flow optimization ● Knowledge of MEP and logistics requirements for large scale, high-volume production facilities ● Experience with ASRS (Automated Storage and Retrieval Systems) warehouse systems, AGV, conveyance, logistics, distribution, RFID and Material Flow Methods is highly desirable ● Experience with system integration to electronic warehouse and asset management systems(EWM/EAM) is highly desirable (preferably SAP) ● Experience designing greenfield facility layouts ● Project Management experience ● Passionate & committed self-starter with “can do” attitude, team player and taking responsibility to get the job done ● Ability to work independent with strong attention to detail and focus on efficiency, effectiveness and cost ● Ability to assess and solve complex issues and tackle problems with limited initial information. ● Intercultural and interdisciplinary communication skills; able to communicate effectively in English (verbal, written) ● Ability to communicate efficiently in Mandarin 【We offer】 ● Competitive compensation package ● Flexible hours and working from home policy. ● Modern working environment with state-of-the-art facilities and technologies ● Challenging assignments in a fast growing and innovative industry ● Position in a dynamic, international team of highly skilled professionals ● Various opportunities for personal and professional development within a global organization

【Job Overview】 This role is embedded in the Molding Technology Group within our Global Operations Engineering team in Taiwan. 【Your responsibilities】 ● Together with the rest of your team you will support the production of injection molded components for our autoinjector systems ● Lead engineering responsibility for molds, component manufacturing and corresponding processes within our production system ● Collaborate closely with shopfloor production technicians, tool makers and maintenance, quality and process development on performance/process improvements and trouble shooting ● Lead the development of improvement plans and requirements for capacity expansion and future mold generations and production setups ● Lead improvement initiatives and capacity deployment in injection molding ● Responsible for manufacturing acceptance of new molds in regular production ● Support Design For Manufacturing (DFM) and definition of manufacturing requirements for new products 【Your qualification】 ● Degree in Mechanical Engineering, Polymer Science or similar education/experience ● Minimum 5 years of relevant industry experience with hands-on experience with multi-cavity hot runner injection molding systems ● Thorough understanding of mold and machine setup, molding machine operation, process optimization, as well as mold design/function. ● Thorough understanding and excellent hands-on experience with auxiliary equipment (i.e. Hot runners, controllers, Polymer dryers, Thermolator, Mold heaters, robot/take out systems, etc.). ● Knowledge of engineering resin characteristics / validation of new polymer materials and molding processes for medical grade polymers. ● Statistical analysis knowledge, including an understanding of how to execute Design of Experiments (DOE). Six Sigma certification is a plus ● Knowledge of common problem-solving and Root Cause Analysis (RCA) methodologies ● Ability to work independent with strong attention to detail and focus on efficiency, effectiveness and cost ● Passionate & committed self-starter with “can do” attitude, team player and taking responsibility to get the job done ● Intercultural and interdisciplinary communication skills; able to communicate effectively in English (verbal, written) ● Ability to communicate in Mandarin is highly desirable 【We offer】 ● Competitive compensation package ● Flexible hours and working from home policy. ● Modern working environment with state-of-the-art facilities and technologies ● Challenging assignments in a fast growing and innovative industry ● Position in a dynamic, international team of highly skilled professionals ● Various opportunities for personal and professional development within a global organization

1.負責抽絲流程的關鍵步驟，包括牽引紗線至後車收取、將殘餘紗線割除等，確保生產過程順利並維持產品品質。 2.定期檢查與保養生產設備，執行簡單的維修與清潔工作，確保機器的正常運行，並減少設備故障或生產中斷。 3.未來表現優異者，將視情況調整薪資，並列為儲備課長人選，培養為技術與管理雙能人才。 4.輪班班別可洽談，並享有輪班津貼。

工作內容 1. 針對代理品牌產品做維修工作 2. 接受原廠維修技術教育訓練 3. 維修技術及工作標準需依據原廠標準施作 4. 負責新人技術指導及說明 5. 協助非代理品牌產品維修工作 6. 該職務需與外國技師對應，需具英文能力中等以上 經歷/技能 1. 安全閥維修經驗2年以上 2. 控制閥維修經驗2年以上 3. 相關閥門維修經驗3年以上 4. 閥門現場維修經驗 艾福特股份有限公司為多家歐美與日本知名專業品牌之閥門與機械設備在台灣的獨家代理商，致力於提供專業銷售與維修服務。 本公司不僅引進多項進口測試設備，更重視專業人才之養成，加入我們，您將有機會： ★學習各式專業知識與實作技能 ★接觸國際大廠的先進技術與作業流程 ★至國外原廠受訓，拓展視野、強化實力 加入艾福特，一起打造技術專業的國際舞台！