Jobs list of Medical Device & Quality Assurance / Quality Control
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NEWJob number: JN -072024-34676 Posted: 2024-09-18
品質保証（QMS担当）
QSR査察の対応経験をお持ちの方必見です。5 - 7 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- Our client is a large industrial manufacturer with various businesses.
- Responsibilities
- 透析装置、消耗品等、同社が扱う医療機器、医薬品のQMS業務：
海外規制に対応したQMSの運用及び他部門への指導
海外当局、PMDA、都道府県、第三者認証機関の監査対応
海外工場のQMS適合性調査
内部監査員として設計、製造部署の内部監査
SOP 改訂
書管理業務
臨床研究（社内倫理審査委員会）及び臨床試験（社内治験審査委員会、実施部門サポート）に関わる業務
ご経験に応じて下記業務もお任せいたします。組織全体に係る品質マネジメントシステムの維持管理業務対応
PMDA、都道府県、第三者認証機関の監査対応
Takahisa Hitotsumatsu
Medical Device -
NEWJob number: JN -072024-34137 Posted: 2024-09-18
PV Manager
Pharma業界の方歓迎10 - 13 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are the Japanese subsidiary of a leading U.S. company in the pharmaceutical and healthcare industry, offering a wide range of products. We provide high-quality and high-performance products and services that cover a broad spectrum from diagnostics to treatment, including diagnostic drugs and devices, pharmaceuticals, hospital products, and nutritional supplements. We have earned high praise for our offerings. Naturally, there is also interdepartmental mobility and information sharing, which helps us maintain our overwhelming position as a comprehensive healthcare manufacturer.
- Responsibilities
- Manage the collection, processing and assessment of safety related information as it relates to the company's Nutrition products in compliance with applicable regulatory requirements and guidelines, as well as division and corporate level policies and procedures; Ensure the pharmacovigilance (PV) system for the company's Nutrition products registered as drugs in Japan is in place and is compliant with regulatory standards; Maintain the PV IT system used for adverse event reporting. The manager is considered a subject matter expert in the area of pharmacovigilance.
Main responsibilities:
Manage the Japan PV team (through guidance and supervision) in the collection, review, and assessment of adverse event reports/safety related information
Ensure submission of reportable adverse events to the health authority in accordance with requirements and timeframes outlined in local regulations
Develop and maintain local standard operating procedures that are aligned with corporate/division level policies and procedures and follow local regulations
Develop and provide PV training for new/junior team members and local affiliate staff
Serve as the point of contact for all local PV activities, inquiries and issues, including responding to inquiries from the health authority
Prepare and submit periodic reports to the health authority in compliance with local regulations
Conduct internal inspections of the PV system as required by local regulations
Serve as the PV lead during internal audits and external inspections; prepare and execute CAPAs for any PV related findings
Participate in the review of promotional materials
Act as the safety database administrator, including coordinating maintenance and upgrades of the PV IT system
Manage vendor and process associated with searching of scientific literature for safety related information
Participate/collaborate with the Medical Safety & Surveillance team on global safety/pharmacovigilance related initiatives and goals
Functions independently as a decision-maker within specified parameters and decisions could potentially have financial ramifications or impact brand reputation, regulatory compliance, or patient and product safety.
Individual is recognized as an internal subject matter expert and resource with responsibilities that require high level critical thinking and analytic abilities.
Leads cross-functional projects related to the area of expertise with a high level of visibility across the local affiliate site.
Responsible for ensuring compliance with local regulatory requirements related to pharmacovigilance for Japan’s drug products.
Shotaro Tsubaki
Medical Device -
NEWJob number: JN -072024-33998 Posted: 2024-09-18
医療機器の品質保証
医療機器もしくは医薬品の品質保証実務経験を３年以上お持ちの方必見です。5 - 7 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- Our client is a medical device manufacturer.
- Responsibilities
- 医療機器の品質保証を担当して頂きます。
品質保証は、自社製品の品質を保ち、さらにお客様からの意見を聞くことで、今後の品質改善に役立てていきます。
そのため、商品の企画開発の段階から、設計、製造、出荷、販売のすべての工程に関わっていただきます。
Takahisa Hitotsumatsu
Medical Device -
NEWJob number: JN -072024-39180 Posted: 2024-09-18
QMS Team Leader (Medical Device) | QMSチームリーダー（医療機器）
医療機器業界でのQMS管理経験が活かせます7 - 11 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- The company is a Japanese optical equipment manufacturer. It engages in the development, manufacturing, and sales of precision measurement equipment. Operating in various fields such as construction, agriculture, and healthcare, it provides surveying equipment and location-based technology. Particularly in the construction industry, it offers automatic control technology for construction machinery and surveying/geospatial information systems to support efficient construction operations. In the agricultural sector, it provides equipment for automatic control of agricultural machinery and devices for precision agriculture, contributing to increased productivity and environmentally conscious farming practices. Furthermore, it develops and provides medical equipment and technology, contributing to the realization of advanced healthcare.
- Responsibilities
- 品質本部QMS課のチームリーダーとして課員をリードしながら、当社におけるQMSの適切な維持管理及び運用をお任せします。※将来的には、本人の希望も勘案し海外駐在も可能
業務内容：
ISO13485に基づいたQMSの維持管理及び、運用内部監査の計画立案、運営による、QMSの適合性維持、有効性の向上
文書管理、マネジメントレビュ、教育訓練、是正予防処置及び測定機器管理に関する実践
医療機器規制当局等（認証機関含む）による審査・査察への対応外部機関による実地監査対応の計画立案、運営、QMS適合性認証取得
外部機関による書面審査時の資料作成及び申請業務
法規制並びに国際規格に関する情報収集並びに各要求事項への適合性の確保
Takahisa Hitotsumatsu
Medical Device -
Job number: JN -072024-169919 Posted: 2024-09-11
【東京】医療機器試験エンジニア ※未経験者歓迎
多種多様な製品開発に携わることができます5 - 10 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are a Japanese subsidiary of a third-party testing and certification organization. We provide quality, technical, safety and environmental services. We help companies meet regulatory and industry standards through evaluation, testing, and certification of products and systems. We also provide risk management and training programs to help companies improve compliance and market competitiveness. We offer services globally, leveraging our expertise in a wide variety of fields to optimize business processes and improve quality. We are trusted by many companies as a reliable third-party organization.
- Responsibilities
- ■業務内容：
電気安全試験およびサイバーセキュリティ試験を主業務とし、試験所の認定に関わる業務もお任せします。
※現時点で医療業界での経験を持ち合わせてない方も当社に入社いただいてから知識・技術を身につけていただけます。
◇電気安全およびサイバーセキュリティ試験業務
試験プロジェクトを遂行いただきます。
国や地域ごとに異なる規格に則った医療機器の安全試験およびサイバーセキュリティ試験
顧客から提出された技術資料（リスクマネジメントファイル、回路図、ソフトウェア資料、取扱説明書等）の評価
試験及び文書評価の結果を基にした試験報告書を作成（英語及び日本語）
顧客との技術ミーティング
進捗管理
◇試験所認定維持活動及びサポート
手順書作成、計測器及び設備管理、認定機関・内部監査の対応
顧客からの問い合わせ対応
顧客先でのセミナー提供
※試験エンジニアとして単独で試験プロジェクトハンドリングが可能となった場合、報告書作成、顧客との打ち合わせ等については遠隔でのリモート勤務も可能です。【変更の範囲：なし】
■ポジションの魅力：
◇多種多様な製品開発に携わることができる
医療機器業界の製造開発では一般的に一つの製品／領域に携わる期間が長期に渡るケースが多く、経験する製品分野が広がらず特化した経験になることが多くあります。
当社では様々な医療機器メーカーの多種多様な製品に関わるため、先端技術の現場に立ち会うこともできます。
視野が広がり、より多くの経験を積み幅の広い経験を積むことが可能です。幅広い領域で医療機器メーカー業界の製造開発に貢献したいという想いをお持ちでしたら、叶えることができる環境が当社にはございます。
◇早期にプロジェクトマネジメント経験を積むことができる
当社であれば1プロジェクトを単独で担当する機会も多いため、早期にプロジェクトマネジメントを経験することができます。
もし自身で裁量を持ち、早期にプロジェクトマネジメントを経験したいという想いをお持ちでしたら、ぴったりな環境だと自負しております。"
Takahisa Hitotsumatsu
Medical Device -
Job number: JN -072024-168584 Posted: 2024-09-11
品質マネジメント
QA部門または業務実施部門にて、安全管理情報の収集や分析、評価、報告、安全確保措置等の業務経験をお持ちの方必見です。6 - 11 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- Our client a major Japanese pharmaceutical company engaged in the research, development, manufacturing, and sales of pharmaceuticals. Our group promotes four business areas—new drugs, generics, vaccines, and OTC products—to meet diverse medical needs. By expanding our operations globally, we aim to provide innovative treatments to a wide range of patients. Additionally, we possess advanced technological capabilities and well-equipped facilities to support our research and development. We actively conduct clinical trials both domestically and internationally, striving to demonstrate leadership in the pharmaceutical industry while emphasizing our commitment to contributing to society as a whole.
- Responsibilities
- 安全管理実施部門またはMA業務実施部門に対して、品質マネジメント担当者として、リスク軽減策のアドバイス、コンプライアンスマネジメントを行う。
GVP/GCP（MA）/GPSP業務に関連する当局査察、外部提携会社による監査への対応業務（査察準備、ファシリテーション、トレーニング等）
マネジメントレビューの実施（品質レポートの作成、指標設定を含む）
GVP/GCP/GPSP関連法規制の適用に関するアドバイスおよび法規制変更時の社内対応推進（手順書改訂サポート、トレーニングを含む）
Patrick Chang
Pharma -
Job number: JN -072024-169704 Posted: 2024-09-11
機能安全認証エンジニア
ハードウェアの開発プロジェクトマネジメント等に関する経験をお持ちの方必見です。5 - 6.5 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are a Japanese subsidiary of a third-party testing and certification organization. We provide quality, technical, safety and environmental services. We help companies meet regulatory and industry standards through evaluation, testing, and certification of products and systems. We also provide risk management and training programs to help companies improve compliance and market competitiveness. We offer services globally, leveraging our expertise in a wide variety of fields to optimize business processes and improve quality. We are trusted by many companies as a reliable third-party organization.
- Responsibilities
- 機能安全認証のプロジェクトマネージメント全般（海外チーム、日本の顧客）
認証業に伴うアセスメント業務（品質マネージメントシステム、ハードウェア、ソフトウェア設計）
試験プランの作成、Review
海外エンジニアを含む、日本人顧客とのミーティング（逐次通訳等）の司会
機械安全、機能安全に関するセミナー、個別トレーニング
Linh Do
Medical Device -
Job number: JN -072024-167398 Posted: 2024-09-11
【東京】アイケア関連製品における安全管理
医療機器業務経験者必見です!5 - 9 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- The company is a Japanese optical equipment manufacturer. It engages in the development, manufacturing, and sales of precision measurement equipment. Operating in various fields such as construction, agriculture, and healthcare, it provides surveying equipment and location-based technology. Particularly in the construction industry, it offers automatic control technology for construction machinery and surveying/geospatial information systems to support efficient construction operations. In the agricultural sector, it provides equipment for automatic control of agricultural machinery and devices for precision agriculture, contributing to increased productivity and environmentally conscious farming practices. Furthermore, it develops and provides medical equipment and technology, contributing to the realization of advanced healthcare.
- Responsibilities
- 安全管理に関する業務全般をお任せします。
GVP省令及び各国・地域のビジランス業務に関わる規程・手順書の策定、維持
安全管理情報の収集、判断の実施
安全確保措置の実施
各国法規に従った規制当局への報告
各国法規に従った市販後調査の実施
法規制に基づく販売業者の監視
主要販社品質保証部門に関する業務との情報連携
Takahisa Hitotsumatsu
Medical Device -
Job number: JN -072024-169082 Posted: 2024-09-11
品質マネジメント・課長
品質マネジメントシステムに関する業務経験をお持ちの方必見です。9 - 12 million yen Kanagawa Medical Device Quality Assurance / Quality Control
- Company overview
- We are engaged in the medical field, specializing in clinical diagnostics. As a leading company in the industry, we provide valuable technologies and biomarker products. Our mission is to create new value in the healthcare market and contribute to the future of health and medicine. Since successfully commercializing products such as the syphilis test kit "Syphilis HA Antigen (TPHA)," we have been involved in research, development, manufacturing, and marketing, bringing innovation to the global clinical diagnostics industry. Particularly as a leading company in the field of immune sera, we have significantly contributed to medical advancement through the development of highly sensitive automated immunoassay instruments and dedicated reagents, as well as the development of rapid immunodiagnostic kits. We have garnered worldwide attention by swiftly succeeding in the development of a rapid antigen test kit for the novel coronavirus (SARS-CoV-2), demonstrating our commitment to providing highly socially impactful and necessary products.
- Responsibilities
- 以下の業務執行における、企画立案、課題解決、PJ推進、要員管理などのマネジメント業務に当たります。
品質マネジメントシステムに関する文書改訂、ＣＡＰＡとりまとめ、データ解析、改善提案、査察対応
他部署の新規業務や改善に対する妥当性確認、検証、改善
ホールディングス各社及び外部関連会社との委託業務の管理や連携業務
Risa Harada
Medical Device -
Job number: JN -072024-23553 Posted: 2024-09-11
Quality Assurance
Manufacturing site in Shizuoka - Gaishi6 - 8 million yen Other Medical Device Quality Assurance / Quality Control
- Company overview
- Our client is a globally recognized distributor of pharmaceuticals, manufacturer and distributor of medical and laboratory products, and a provider of performance and data solutions for healthcare facilities.
- Responsibilities
- 滅菌バリデーションン責任者もしくは生物由来製品製造管理者として滅菌保証活動もしくは生物由来製品の管理を行う
滅菌保証にかかわる運営責任を有し、滅菌保証に関連する発生した問題への対処、および問題発生を予防する活動を計画・実行する
試験業務の運営及び継続的改善を行う
滅菌保証チーム員及び試験員の労務管理及び人材育成
滅菌保証チーム員及び試験員の活動にかかわる安全管理、文書管理及び経費管理
Linh Do
Medical Device -
Job number: JN -072024-22567 Posted: 2024-09-11
品質保証業務
日系大手医療機器メーカー 品質保証6 - 9 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are a major corporation based in Japan, offering a wide range of products and services. Beyond just photographic film and cameras, we also specialize in medical equipment, chemicals, optical devices, and more. Our focus is on the quality, innovation, and sustainability of our products, providing value to customers worldwide. Additionally, we prioritize research and development, contributing to advancements in science and technology.
- Responsibilities
- （1, 2, 3のいずれか）体外診断用医薬品や医療機器の品質保証業務、又は、品質管理システム（QMS）スペシャリスト体外診断用医薬品の製造販売業者としての品質保証業務（国内、海外）
X線診断装置、マンモグラフィーの製造販売業者としての品質保証業務（国内、海外）
同社のQMSの管理運営、及び、監査・査察対応業務（MDSAP、MDR/IVDR、FDA査察、適合性調査他）
Go Ozawa
Medical Device -
Job number: JN -072024-22568 Posted: 2024-09-11
内視鏡品質保証業務
日系大手医療機器メーカー 内視鏡品質保証業務6 - 10 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are a major corporation based in Japan, offering a wide range of products and services. Beyond just photographic film and cameras, we also specialize in medical equipment, chemicals, optical devices, and more. Our focus is on the quality, innovation, and sustainability of our products, providing value to customers worldwide. Additionally, we prioritize research and development, contributing to advancements in science and technology.
- Responsibilities
- 内視鏡システム製品及び関連製品の品質保証業務、および、品質管理システム(QMS)スペシャリスト内視鏡製品の製造販売業者としての品質保証業務(国内、海外)
内視鏡開発のQMSの管理運営、及び、監査・査察対応業務(MDSAP、MDR/IVDR、FDA査察、適合性調査他)
Go Ozawa
Medical Device -
Job number: JN -072024-15941 Posted: 2024-09-11
HQ QA
Japanese multinational IVD maker5 - 7 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are engaged in the medical field, specializing in clinical diagnostics. As a leading company in the industry, we provide valuable technologies and biomarker products. Our mission is to create new value in the healthcare market and contribute to the future of health and medicine. Since successfully commercializing products such as the syphilis test kit "Syphilis HA Antigen (TPHA)," we have been involved in research, development, manufacturing, and marketing, bringing innovation to the global clinical diagnostics industry. Particularly as a leading company in the field of immune sera, we have significantly contributed to medical advancement through the development of highly sensitive automated immunoassay instruments and dedicated reagents, as well as the development of rapid immunodiagnostic kits. We have garnered worldwide attention by swiftly succeeding in the development of a rapid antigen test kit for the novel coronavirus (SARS-CoV-2), demonstrating our commitment to providing highly socially impactful and necessary products.
- Responsibilities
- 品質保証部門において市販後製品情報対応業務の担当者を募集します。本ポジション（品質保証部市販後製品情報課）は試薬・装置の苦情に関する調査や他部署との折衝の他、グループ会社の依頼によるデータ取得業務（測定業務）、欧州規制要求改正（IVDR）に伴う市販後製品情報についての報告業務や、製品の市中販売による苦情対応と多岐にわたっており、製品数、ユーザー数の増加に伴い社内の重要性も増しているポジションです。製品関連苦情に基づいて、社内外製造元や開発へ苦情調査の指示、調査結果に基づく苦情報告書の作成
市販後製品情報の集計分析。装置・試薬の改善に向けた取り組み
安全管理責任者を補佐し、安全管理情報の収集、安全確保措置に伴う市場・規制当局対応、GVP契約委託先との契約管理を実施
市販後製品情報（MDR）の定期的なUpdate及び維持
研究開発などの他部署やその他装置製造元など社外との情報交換・連絡会等
Linh Do
Medical Device -
Job number: JN -072024-4098 Posted: 2024-09-11
【幡ヶ谷】品質保証
大手日系企業の品質担当5.5 - 7.5 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are a leading Japanese manufacturer and distributor of medical devices and related products. We have a particularly strong reputation in the field of medical devices, such as catheters and artificial heart-lung machines, and we are expanding our business widely both domestically and internationally. We are also expanding into the fields of pharmaceuticals and blood systems, providing comprehensive medical solutions. We focus on innovation and quality control, and develop our products with patient safety and healthcare professionals\' convenience in mind. We aim to contribute to the development of healthcare from a global perspective and are actively involved in the realization of a sustainable society.
- Responsibilities
- 品質マネジメントシステム改善
各国規制への適合化に関する業務
Shotaro Tsubaki
Medical Device -
Job number: JN -072024-33523 Posted: 2024-09-11
Safety Specialist
理系卒未経験の方歓迎6 - 10 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- Our client is the global technology leader in minimally invasive surgery.
- Responsibilities
- Manage and implement required actions to maintain existing product lines and to solve any product quality issues occurred in Japanese market. Take timely and appropriate quality management actions and executing communications with government and internal / external customers. This position has mainly following responsibilities and authorities to timely deliver effective and safety products in Japanese market, to reduce customer complaint/malfunction, and to improve product quality:
Main responsibilities:
Lead risk management team and implement risk management activities from the viewpoint of product and subcontractors / suppliers in cooperation with related functions.
Assess change notifications from headquarters and manufacturing sites, and implement necessary actions in cooperation with related functions.
Evaluate customer complaints from the viewpoint of product quality, report to company and manufacturing sites, and evaluate the analysis result in cooperation with Safety Control team. Furthermore, create customer letters, and communicate to customers to solve the quality issue with Marketing, Sales, Field Service and Safety Control teams.
Completing quality issues by working with regulatory agencies, customers and related functions.
Collaborate with Product Quality team and Safety Control team to reduce customer complaints from the viewpoint of product.
Involve in implementation of a field action like a recall.
Collaborate with QRC team to maintain Quality Management System.
Work related to product realization (control DMRs and materials for released products etc.)
Operate product release (IQC, labeling instructions, and market release assessment etc.)
Manage non conforming products (rework, concession, and hold etc.)
Work related to data analysis and CAPA.
Shotaro Tsubaki
Medical Device -
Job number: JN -072024-38982 Posted: 2024-09-11
General Manager | 総括マネージャー
Gloabl life science & diagnostics company11.5 - 13 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are a leading biotech company in the healthcare industry, attracting attention for our excellence. We specialize in diagnostic pharmaceuticals and equipment, taking charge of the diagnostic segment within our group. As one of the pillars of our operations, we focus on providing high-quality and accurate diagnostic products for a wide range of diseases, including cancer, cardiovascular diseases, and infectious diseases.
- Responsibilities
- QMS省令に基づく総括製造販売責任者業務、およびクオリティーマネジメントグループのマネジャーとして業務いただきます。詳細は以下の通り。
業務内容：
品質保証・安全管理業務の統括、チーム管理及びメンバー育成安全管理業務に対する総括製造販売責任者としてのアドバイス、確認、および承認
製品への出荷可否判定にかかわる業務の監督
苦情、品質不良などの所要措置の決定および実施
各製造所（外国製造所を含む）の製造管理・品質管理にかかわる業務
国内業許可管理業務の監督
化学物質関連規制や海外HQ要求事項の国内対応の監督
規制当局や海外HQの監査対応、および内部監査、教育訓練、管理監督者照査の実施
海外HQとのコミュニケーション（QMS関連対応、化学物質関連規制対応、品質問題対応など）
QMS省令に基づく総括製造販売責任者業務、およびクオリティーマネジメントグループのマネジャーとして業務いただきます。詳細は以下の通り。品質保証・安全管理業務の統括、チーム管理及びメンバー育成
安全管理業務に対する総括製造販売責任者としてのアドバイス、確認、および承認
製品への出荷可否判定にかかわる業務の監督
苦情、品質不良などの所要措置の決定および実施
各製造所（外国製造所を含む）の製造管理・品質管理にかかわる業務
国内業許可管理業務の監督
化学物質関連規制や海外HQ要求事項の国内対応の監督
規制当局や海外HQの監査対応、および内部監査、教育訓練、管理監督者照査の実施
海外HQとのコミュニケーション（QMS関連対応、化学物質関連規制対応、品質問題対応など）
Linh Do
Medical Device -
Job number: JN -072024-34281 Posted: 2024-09-11
品質保証/QA
ライフサイエンス市場及び製品に関する幅広い業務知見をお持ちの方必見です。7.3 - 8.8 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- We are a global provider of diagnostic, medical device, healthcare IT, and life science products and services for a wide range of customers, from research to diagnosis, treatment, and prevention. We are committed to quality and innovation, utilizing the latest science and technology. Our products and services contribute to accurate diagnosis, treatment, and health care in the medical field. We also value collaboration with research institutes and medical institutions to contribute to the advancement of medicine and human health. Our business model is sustainability oriented and socially responsible.
- Responsibilities
- グローバルでトップクラスシェアを有するバイオメディカ事業部の品質保証部では、今後グローバルオペレーションの強化（海外の販売会社・工場・購入先とのコミュニケーション強化）、新規事業や新規製品のQMS確立、長期的な高精度品質保証を継続的に実現するため、品質監査主担当（リーダー候補）ポジションを募集します。
業務内容：
内部品質監査、購入先品質監査、外部委託先品質監査、及び監査結果のまとめと報告、是正確認
工場、外部委託先工程の品質向上に向けた支援活動
購入先の品質向上に向けた支援活動
品質マネジメントシステム運営のサポート
Takahisa Hitotsumatsu
Medical Device -
Job number: JN -072024-150828 Posted: 2024-09-11
Quality Assurance - Eye Care Products | アイケア関連製品における品質保証
日系安定成長企業・顧客満足度を向上させる重要な役割を担っていただきます7 - 12 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- The company is a Japanese optical equipment manufacturer. It engages in the development, manufacturing, and sales of precision measurement equipment. Operating in various fields such as construction, agriculture, and healthcare, it provides surveying equipment and location-based technology. Particularly in the construction industry, it offers automatic control technology for construction machinery and surveying/geospatial information systems to support efficient construction operations. In the agricultural sector, it provides equipment for automatic control of agricultural machinery and devices for precision agriculture, contributing to increased productivity and environmentally conscious farming practices. Furthermore, it develops and provides medical equipment and technology, contributing to the realization of advanced healthcare.
- Responsibilities
- 当社アイケア製品の品質保証に関する業務全般をお任せします。
業務内容：
苦情内容に関する調査・分析
苦情情報の調査・分析に関する品質改善指示
苦情の是正と予防対応
出荷停止及び解除に関する業務
回収/改修に関する業務
製造販売後の法規制に関する業務
Go Ozawa
Medical Device -
Job number: JN -072024-150829 Posted: 2024-09-11
Quality Assurance (Post-Marketing Surveillance) | 品質保証（市販後調査）
高クラス医療機器の市販後調査・将来的に安全管理責任者としてご活躍いただける可能性有5 - 8 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- Our client is a medical device manufacturer.
- Responsibilities
- 医療機器の市販後監視活動（PMS）安全管理業務（GVP）をご担当いただきます。
業務内容：
文献調査、クレーム分析、トレンド分析、類似医療機器の公開情報分析等
安全管理業務（安全性情報収集・評価・分析）
不具合に関する報告書の作成、国内外の行政機関に対する報告・対応
各国の法規制への対応・各国の行政との折衝
担当チームのマネジメント業務
※将来的には、安全管理責任者としての業務を行っていただく可能性があります。
Go Ozawa
Medical Device -
Job number: JN -072024-149604 Posted: 2024-09-11
Quality Control | 品質管理
高クラス医療機器の品質管理・将来的にマネジメント業務も担っていただく可能性あり5 - 7 million yen Tokyo Medical Device Quality Assurance / Quality Control
- Company overview
- Our client is a medical device manufacturer.
- Responsibilities
- メディカル部門の品質管理担当者として以下の業務に従事いただきます。
業務内容：
ガイドワイヤー、カテーテル等の弊社ブランド製品の品質管理業務品質管理
変更管理
不適合品管理
計測器管理
評価
データ分析
改善等
滅菌プロセスの維持・管理各バリデーション
法規制対応
監査対応 等
品質保証業務法規制対応
監査対応 等
開発プロセスにおけるＱＭＳ視点のチェック、管理
医薬品医療機器等法、ＱＭＳに基づく記録の作成、管理
※ 将来的に現地でのマネジメント業務の可能性もあります※国内外転勤可能性ありますが、当面はございません。
Go Ozawa
Medical Device