Job Description Main Responsibilities: Support the Quality Assurance activities of the Marketing Authorization Holder as described below: Ensure the implementation of GQP Quality Assurance activities and ensure activities operate within established policies/procedures, global requirements, and all applicable regulations.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new
Mujin has transformed the field of industrial automation with its innovative robot control technology and is currently revolutionizing supply chains worldwide. Today, we are rapidly expanding our business both domestically and internationally, serving clients from Japan
Mujin has transformed the field of industrial automation with its innovative robot control technology and is currently revolutionizing supply chains worldwide. Today, we are rapidly expanding our business both domestically and internationally, serving clients from Japan
Our vision is to transform how the world uses information to enrich life for all. Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring
Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new
Job Description Job Summary: To ensure that clinical supplies are stored and distributed in accordance with Fisher Clinical Services (FCS) approved procedures and policies, cGMP, cGDP, and regulatory requirements. Maintain the FCS Japan Quality System in compliance with
職務 概要 Position Summary : • This Job Description applies to the position of Operational Quality Group Staff at JPKK, Fuji Plant. • This individual provides quality perspective direction for all production activities at JPKK, Fuji Plant 法規制の順守に関する責任
Company Description SoC products for automotive applications are key components for the realization of electronic and advanced functions in automobiles, and their development is unabated. However, as a result of higher performance and functionality than ever
Johnson & Johnson is the worlds most comprehensive and broadly-based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in pharmaceutical, and medical devices and
Johnson & Johnson Innovative Medicine (JJIM) is recruiting for a(n) Quality Control Senior analyst, located in Janssen Fuji Site, Japan. This position is responsible for leading analytical method transfer for NPI to implement in country test. The
SCOPE OF THE ROLE AND BASIC PURPOSE Responsible for overall quality and compliance action such as complaint handling, field action, change control and so on in Japan market for DePuy Synthes Joint Digital Biomaterial and Spine (JDBS)
Görev Tanımı The Position Individual contributor is accountable for ensuring all activities at the External Entity (EE) site associated with the manufacturing of Company products which includes quality oversight over manufacturing, testing, packaging, storage, and distribution of
8/6 roster - FIFO from Perth to the Roy Hill mine Work for an expanding and high performing iron ore business Performance, Retention and Profit Share Bonuses Fly with Qantas with access to QFF points and
Job Description Summary ノバルティスの品質マニュアルとポリシーに基づき、現地規制の下、以下のことを達成する。 - 品質管理- 原料、製剤、最終製品の試験・検査を通じて製品の品質管理を行う。 - GMP/ GCTP（Good Gene, Cellular, and Tissue-based Products Manufacturing Practice：遺伝子・細胞・組織関連製品の適正製造規範）に基づき規制遵守を維持する。 - HSE- 日本の規制要件およびノバルティスのHSEポリシーに基づき、職場環境をモニターし、適切に維持する。 Job Description 主な役割責任 以下の業務が適切に行われていることを保証する。 原料、包装材料、原薬のサンプリングおよび受入試験 医薬品の最終製品の出荷試験 安定性モニタリング 環境モニタリング 品質管理記録の照査 品質管理部門の文書システムを管理する。 機器の校正、部門施設および機器のメンテナンスを適切に実施されていることを保証する。 試験室を維持する（文書、ガラス器具、試薬・試液、機器など）。 標準品（一次及び二次）が適切に取り扱われていることを保証にする。 すべてのチームメンバーに対して適切なトレーニングが実施されていることを保証する。 必須要件 薬学または化学の学士号以上をお持ちであること
Job Description Summary The Senior Engineer – CT (Computed Tomography) Systems will design CT products with each sub-system team and deliver CT system with the highest quality. CT Systems Senior Engineer is considered as an expert in CT Systems and key components
職務内容 Key Accountabilities Country Quality System management Lead the implementation and maintenance of GxP quality system with respective operation units, the continues quality system implementation for competencies and related Quality documentation of GxP area: medical, pharmacovigilance, regulatory and clinical. Deviation and CAPA management:
MI Systems Maintainer Integrator II - TS/SCI Job Category: Engineering and Technical Support Time Type: Full time Minimum Clearance Required to Start: TS/SCI Employee Type: Regular-Long Term Assignment Percentage of Travel Required: Up to 10% Type of
JOB SUMMARY On the basis of Sanofi quality policy and Japanese regulations, make available to customers high quality products and services through promoting Quality Assurance activities strongly and leading / supporting Japanese Contract Manufacturing Organization in order to ensure
