相关搜索

ContextWorks either in Customer Support or in BL Apps (AE, Brion or HMI) and can be located in the field as well as at HQ working on sustaining, NPI or customer projects. Interfaces with project leaders and mostly within own sector or project team.Has skill set of multiple competencies to practically make use of knowledge base to resolve issues that have...

DescriptionPosition Summary:This position is responsible for the continued development and maintenance of Garrett’s China & Japan import-export compliance program. The Trade Compliance Leader will provide leadership and expertise in ensuring China & Japan trade compliance for Garrett Motion.This role has direct responsibility for overseeing China & Japan...

About MarvellMarvell’s semiconductor solutions are the essential building blocks of the data infrastructure that connects our world. Across enterprise, cloud and AI, and carrier architectures, our innovative technology is enabling new possibilities. At Marvell, you can affect the arc of individual lives, lift the trajectory of entire industries, and fuel...

System Development Engineer acts as the function owner for high-voltage product systems, who can define inverter or MCU(Motor Control Unit) product requirements, cooperate with software and hardware team to implement system strategy design, and finally implement product issue trouble-shooting and participate in putting forward final solution to improve...

Job Description SummarySystem Development Engineer acts as the function owner for high-voltage product systems, who can define inverter or MCU(Motor Control Unit) product requirements, cooperate with software and hardware team to implement system strategy design, and finally implement product issue trouble-shooting and participate in putting forward final...

Job SummaryJob Description(1)    Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan;(2)    Establish inspection criteria of new finished products, update and maintain inspection criteria for existing products on Medline quality management platform (ETQ)(3)  ...

Job Summary Associate QA specialist is the role who responsible for quality assurance on the procedures of DMR and inspection criteria data maintenance. Implement the actions under supervisor’s supervision to ensure requirements are met under ISO13458 and CFR820. Job Description (1)    Assist in collecting and verifying Device Master Record (DMR)...

Job SummaryAssociate QA specialist is the role who responsible for quality assurance on the procedures of DMR and inspection criteria data maintenance. Implement the actions under supervisor’s supervision to ensure requirements are met under ISO13458 and CFR820.Job Description(1)    Assist in collecting and verifying Device Master Record (DMR) documents...

Third Bridge is a leading global research firm established in 2007, with a team of over 1,500 employees worldwide dedicated to fueling decisions with expert insights. We accelerate and enhance decision-making for investors and business leaders by unearthing unique expert insights across multiple sectors, geographies, and topics. For nearly 20 years, we’ve...

About MarvellMarvell’s semiconductor solutions are the essential building blocks of the data infrastructure that connects our world. Across enterprise, cloud and AI, and carrier architectures, our innovative technology is enabling new possibilities. At Marvell, you can affect the arc of individual lives, lift the trajectory of entire industries, and fuel...

DescriptionJob Summary: Under minimal supervision and in accordance with Cummins Delegation of Authority Policy, determines the quantity and order date for materials needed to meet the master production schedule or independent customer demand. Expedites purchase or production orders as appropriate.   Key Responsibilities: Health, Safety & Environmental...

Job SummaryJob Description1.    Perform QMS audit to vendors, write audit report, and follow-up supplier CAPA.2.    Work as project leader in Vendor FDA project, supervise vendor to adequately establish and maintain QMS based on 21CFR820, work with vendor to deal with FDA onsite audit, act as consultant to help vendor establish a better QMS with...

该职位来源于猎聘 Key Responsibilities: Responsible for Trade Compliance in China & Japan Lead and support Government, customs authorities and internal audits; Conduct Customs compliance on site review/self-assessment, define corrective actions, and lead execution on compliance improvement plan and support sites with implementation; Responsible for...

Description JOB SUMMARY   Assists the Front Office Manager in administering front office functions and supervising staff on a daily basis. Front office areas include Bell/Door Staff, Switchboard and Guest Services/Front Desk. Position directs and works with managers and employees to carry out procedures ensuring an efficient check in and check out process....

****Who We Are**** Emerald Clinical Trials is a **global leader** in clinical research, partnering with over **160 biotech** companies and **15 of the world’s top 20** pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases,...

Job Summary Job Description (1) Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan; (2) Establish inspection criteria of new finished products, update and maintain inspection criteria for existing products on Medline quality management platform (ETQ) (3) Maintain...

**Job Summary** **Job Description** 1.    Perform QMS audit to vendors, write audit report, and follow-up supplier CAPA. 2.    Work as project leader in Vendor FDA project, supervise vendor to adequately establish and maintain QMS based on 21CFR820, work with vendor to deal with FDA onsite audit, act as consultant to help vendor establish a better...

**Job Summary** **Job Description** (1)    Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan; (2)    Establish inspection criteria of new finished products, update and maintain inspection criteria for existing products on Medline quality management...

JOB TITLE JOB FAMILY DATE Quality Engineer QUALITY 01/06/2020  MANAGER TITLE (solid line) FUNCTIONAL MANAGER TITLE (dotted line) Quality Engineer leader         MISSION In one or two sentences, outline the primary purpose(s) of this position within the organization   * Ensures that quality rules and methods are deployed and followed...

该职位来源于猎聘 Position Summary Weidmann is seeking a technically skilled and self-driven IT Infrastructure Specialist to support the planning, implementation, and maintenance of IT infrastructure across the Asia Pacific (AP) region. This role places a strong emphasis on network and data center design, server and printer infrastructure, and...