自動車の内装部品(プラスチック部品)を製造する 射出成形機のオペレーター業務をお任せします。 · ...

Deffabrikkens produksjonsarbeidet · Måtte ha erfaring med maskiner? Ingen problem! Vi er der du kan lære hvordan vi produserer deler som er nødvendige for våre kjøretøy. · må kunne operere maskiner · ...

アマダ製タレットパンチを使用して、材料加工の段取り、セット作業、バリ取りなどを行っていただきます。作業工程管理やそれに付随する補助業務も行っていただきます。 · ...

募集するのは「プラスチック成型技術者」のポジション。経験を活かし、一緒に支えていっていただける方をお待ちしています · 仕事内容 · 自動車部品などの精密プラスチック製品の成形業務の他、測定業務をお任せします。 · 具体的には · ...

Job Title: Tolling Coordinator Summary: We are looking for a Tolling Coordinator to support our growth strategy by outsourcing some manufacturing tasks. The role will involve working with internal and external stakeholders to plan and implement procurement strategies, managing in ...

Tolling Coordinator role involves supporting company growth by outsourcing manufacturing to external partners. Duties include procurement planning, inventory management, and KPI-driven improvement activities. · ...

A Field Engineer at GE HealthCare will maintain equipment across their designated area by performing routine inspections maintenance repairs maintenance claims management etc. · ...

上下水道の配管部品や自動車・医療機器などに使われるプラスチック製品の製造に携わり品質と技術の向上に力を注ぎながら最高の製品をお客様に提供する当社。順調に成長を続けている安定企業です。今後も可能性とチャンスが待っている会社であなた自身の未来も切り開いていきませんか? · ...

旟す（driveshaft） · ！automatic processing machine operated by human. · ...

We are looking for a Field Engineer to join our team in Maebashi. The successful candidate will be responsible for maintaining medical equipment and devices, providing customer support and quality management. · ...

This position involves engineering work such as manufacturing adjustment and inspection of automatic inspection machines for pharmaceuticals at Syntegon Technology K.K. · General manufacturing adjustment and inspection work for automatic inspection machines for pharmaceuticals · ...

+ Design specifications · +  ic software design · +  customer-submitted documents · +Troubleshooting management · The position involves engineering work on automatic inspection machines for pharmaceutical manufacturing lines at Syntegon Technology K.K., Japan's subsidiary of Synt ...

This position involves engineering work such as manufacturing adjustment inspection of automatic inspection machines for pharmaceuticals at Syntegon Japan one of the worlds largest manufacturers of various packaging machines. · ...

自動車車載品メーカー プラスチック射出成形 · 群馬県伊勢崎市三和町2718-3 · 正社員 · ...

This position is responsible for engineering work on the company's products (automatic inspection machines) for automated pharmaceutical inspection lines at the Japanese subsidiary of Syntegon. · ...

This position is responsible for field engineering work for new installations and after-sales service of Syntegon's products at the Japanese subsidiary of Syntegon. · Work at customer sites (parts replacement, troubleshooting, improvement work, modification work) for ampule and v ...

We are seeking a Staff Modeling and Characterziation Engineer to characterize and model FETs, · Providing modeling support to develop novel high-performance power switching device technology · Closely working with device engineers toward optimizing the FETs for switching applica ...

We are seeking a Regulatory Affairs Specialist to join our team at Johnson & Johnson. In this role you will be responsible for maintaining regulatory approval for general surgery products such as sutures and adhesives. · ...

We are seeking an Account Manager to join our team in Tokyo. As an Account Manager, you will be responsible for developing and maintaining relationships with key customers in the manufacturing, electronics, and automotive industries. · ...

This team supports SPS FET design for PCP. We currently have limited characterization ability and no modeling. The SPS FETs are critical for PCP and we are entering a period of incredible growth for SPS FETs where we are looking at volume sales increasing by 3x in the next 2 year ...

+We are seeking a Regulatory Affairs Specialist to join our team in Chiyoda, Tokyo. The successful candidate will be responsible for developing and implementing regulatory strategies for medical devices. Key responsibilities include preparing and submitting regulatory application ...