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Jobs list of Pharmaceutical & Quality Assurance / Quality Control

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  • NEW
    Job number: JN -052025-187800 Posted: 2025-05-09

    精密化学品の品質保証職

    医薬品に関する品質保証経験をお持ちの方必見です。
    5.41 - 9.28 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    Our client is a trading company that mainly deals in chemical products and physics and chemistry equipment.
    Responsibilities
    マスターファイルの作成及び登録申請(照会対応含む)
    製造業の更新申請及び外国製造業者の認定申請
    医薬品原薬・中間体、化学品に関する品質保証業務
    GMP管理、品質システムの構築及び遂行業務
    製造記録・試験記録の照査業務
    サプライヤーの監査業務
    お客様からの問い合わせ初期対応、並びに一部代理店の管理
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -022025-184130 Posted: 2025-05-02

    品質保証

    医薬品や医療機器の品質保証部門での業務経験をお持ちの方必見です
    7 - 8.5 million yen Shizuoka Pharmaceutical 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
    同社は5万点以上の製品を160以上の国と地域に展開している総合医療機器メーカーです。2023年度は過去最高の売上収益・営業利益・当期利益額を更新し、売上高1兆円規模も目前に迫っています。 
    同社において、工場における品質保証担当を増員募集します。現在工場におけるGMP/QMSの維持管理業務のボリュームが増加しており、特に製品品質照査業務は、法的要求である医薬品だけでなく、顧客要求事項から医療機器への展開も必要となっている背景から、品質文書経験をお持ちの方をお迎えしたい考えです。独自の技術力によって各製品群で高シェア率を獲得しており、医療現場への影響力の大きい企業で、次のキャリアを築きませんか?
    ■業務内容:
    製品品質照査(品質文書レビュー)業務:製造記録や品質試験記録から得られる管理指標が1年を通して安定しているかトレンド的な視点で評価し、報告書を作成します。
    変更管理業務  
    文書管理業務

    ━━━━━━━━━━━━━━━#poweredjob2
    Takahisa Hitotsumatsu
    Takahisa Hitotsumatsu
    Medical Device
  • Job number: JN -072024-35013 Posted: 2025-05-01

    医薬品の品質保証

    医薬品業界もしくは医療機器・食品・化粧品メーカー等類似技術を使用した業界の品質保証業務経験がある方必見です。
    5 - 10 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    Our client is a pharmaceutical manufacturer.
    Responsibilities
    治験薬、医薬品のGMP、GDP管理業務ならびに薬制対応業務
    同社で扱う医薬品及び治験薬の製造・品質試験における品質保証業務全般を担当します。製造・品質試験における各プロセスの品質保証業務
    逸脱管理、変更管理、CAPA管理、出荷管理
    医薬品品質システムの運用推進(教育、文書管理、等)
    各工場の知見集約(知識管理)とサイト横断的な医薬品品質システムの構築(共通化・効率化)
    新製品や新規設備の技術移転、クオリフィケーション、バリデーション
    国内外の当局GMP査察対応
    業者管理(原材料サプライヤー等)

    Patrick Chang
    Patrick Chang
    Pharma
  • Job number: JN -072024-38866 Posted: 2025-05-01

    Quality Assurance Senior Manager

    Full Remote QA Senior Manager position
    12 - 15 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    The company is a foreign-affiliated pharmaceutical company.
    Responsibilities
    Provide strong support team management for GQP Head on day-to-day basis
    Plan, organize and lead periodic internal reviews with all stakeholders (e.g. GM, Audit, Supply Chain, launch management, Regulatory affairs and Cooperate Quality compliance)
    Qualify, manage, support and supervise assigned CMO and API suppliers aligned with local regulation and the company Quality Management Systems and provide reports as required
    Implement, report and monitor CMO Quality Metrics and ensure identification and implementation of improvements needed through routine review
    Manage (initiate and investigate) all significant quality issues associated with Drug Products or APIs originating from assigned CMO or suppliers (complaints, deviations, recalls, counterfeits and product tampering, stability failures, etc.) appropriately and in a timely fashion
    Provide support to develop/implement/maintain/improve QMS in line with local regulation and company QMS
    Perform other duties as assigned such as described below, but are not limited to:
    Provide support for regulatory agency inspection readiness and requests
    Maintain an annual auditing program, participate in technical visits and/or audits, manage action plans and follow up on agreed upon CAPAs
    Support business develop

    Yui Osone
    Yui Osone
    Pharma
  • Job number: JN -072024-34686 Posted: 2025-05-01

    Quality Assurance Specialist

    Global, top market share company / international atmosphere
    4 - 8 million yen Shizuoka Pharmaceutical Quality Assurance / Quality Control

    Company overview
    Our client is a contract manufacturer of soft capsules for pharmaceuticals and health foods.
    Responsibilities
    製造・品質管理の監督
    変更管理・逸脱管理・出荷管理
    品質情報(顧客クレーム)対応
    バリデーション・教育
    製造記録・品質試験記録の照査
    新規プロジェクトの推進
    Yui Osone
    Yui Osone
    Pharma
  • Job number: JN -072024-137933 Posted: 2025-05-01

    QA Manager

    QA Manager
    10 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are engaged in the research, development and provision of medical technologies in Japan. In particular, we focus on the development of innovative therapies and provide advanced technologies related to cancer treatment. We use a new therapeutic approach called photoimmunotherapy to target cancer cells for effective treatment. This technology combines light and drugs to selectively destroy cancer cells. In research and development, we are strengthening our collaboration with specialized institutions and universities in Japan and overseas to conduct clinical trials and commercialize the technology. We are committed to innovation in the medical field and to improving the quality of life of patients.
    Responsibilities
    Support Quality Assurance supervisor to achieve Japan Commercial Operations objectives from Medical device and drug perspective.
    When Quality Assurance issue arises, lead to define the appropriate Quality measurement through the communication with the related internal, global and external parties.
    Ensure full compliance with applicable regulations in Japan.
    Oversee all activities or responsibilities that are delegated to external parties.
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -072024-143827 Posted: 2025-05-01

    品質保証 QA

    Global Company
    6 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
    Responsibilities
    医療機器、再生医療製品等を含む新たなモダリティへの業務展開
    新たな技術の導入、技術の進化
    サプライチェーンの多様化


    グローバル製品(開発品・市販品)の増加
    製造委託先、試験委託先ならびに原材料供給業者の増加
    そのため、GQP/GMP/QMS/GCTP/GDP等に関する品質保証業務に精通した要員の補充が必要となった。


    IND/IMPD、NDA/BLA作成及び推進、国内申請資料作成及び推進、その他CMC薬事にかかわる業務 
    Patrick Chang
    Patrick Chang
    Pharma
  • Job number: JN -072024-145099 Posted: 2025-05-01

    [Tokyo/Shizuoka/Ibaraki] QA for Drug Development and New Product Launch

    Rich Pipeline and Global Culture
    7 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are a leading pharmaceutical company in Japan, offering a wide range of products in the medical field. Our product lineup includes various pharmaceuticals to support patient health, and we are also dedicated to research and development. We strive to develop new treatment methods and medications to contribute to the treatment and prevention of diseases. Additionally, we operate globally, providing our products to patients worldwide. We uphold high standards of quality and safety, contributing to the advancement of healthcare and the well-being of patients.
    Responsibilities
    Contribute to development projects by ensuring the quality of investigational drugs used in clinical trials conducted globally and complying with regulations such as GMP.
    Promotion of quality assurance operations such as management of investigational drugs, investigational drug substances and new product manufacturing contractors, change management in the development phase, implementation of quality audits, shipment of investigational drugs by appropriate product quality management, etc.
    Building and collaborating with joint development partners
    Improvement of global quality assurance system for developed products, continuous improvement, promotion of new regulation compliance
    Promote regulatory inspection response and inspection preparation in cooperation with related departments such as laboratories, manufacturing contractors, and supply chains so that early application and launch of new products can meet and respond to regulatory requirements globally.
    Participate in the global working team within Quality Assurance and Quality Technology to solve quality assurance issues and improve and improve the quality assurance system.
    Initial development phase Quality assurance work at product manufacturing plants such as regenerative medicine
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -022025-184806 Posted: 2025-04-30

    [MSD]Medical Advisor Ophthalmology

    医薬品業界での品質保証のご経験をお持ちの方必見です
    5 - 9 million yen Saitama Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are a leading life sciences company based in the United States, with a parent company. Our core business revolves around the research, development, importation, manufacturing, and sale of pharmaceuticals and vaccines. Every day, we strive towards our mission and goals by protecting people\'s health and helping them build fulfilling lives. We aim to promptly address unmet medical needs in Japan and globally. Furthermore, we actively engage in activities to promote access to medicines, including product donations and supply to those in need through various programs and partnerships.
    Responsibilities
    品質マネジメントシステム&コンプライアンス課では、製造所が医薬品医療機器等法及びGMPコンプライアンスを遵守し、患者さんに提供する医薬品品質の確保及び安定供給を達成するために、品質保証として品質マネージメントシステム(QMS)の構築およびその運営管理を行っております。グローバル標準で一貫性を持った品質、コンプライアンス管理を行い、かつ日本の要求事項への対応も行うため、海外本社および海外サイトをはじめ、規制当局および他社とのコミュニケーションも多くとてもやりがいのある職務です。
    昨今の度重なる医薬品業界における不祥事を発生させないためには、経営層との統制の取れたQMSの運営は欠かせないものであり、このポジションはグローバルグループの一員として、サイトの品質保証として非常に重要なキーポジションになります。【品質マネジメントシステムのトピックリード】査察対応/自己点検
    GMP適合性調査  
    CAPA管理
    データインテグリティ
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -012025-182606 Posted: 2025-04-22

    【本社】医薬品の品質保証 ※年休124日/住宅手当など福利厚生も充実◎

    世界売上トップレベルの米国外資系製薬企業
    7 - 13 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are a leading life sciences company based in the United States, with a parent company. Our core business revolves around the research, development, importation, manufacturing, and sale of pharmaceuticals and vaccines. Every day, we strive towards our mission and goals by protecting people\'s health and helping them build fulfilling lives. We aim to promptly address unmet medical needs in Japan and globally. Furthermore, we actively engage in activities to promote access to medicines, including product donations and supply to those in need through various programs and partnerships.
    Responsibilities
    ◇◆◇世界売上トップレベルの米国外資系製薬企業、唯一の国内工場で品質保証担当者を募集いたします◇◆◇
    新薬の承認申請を見越した体制強化のための増員募集を行っております。品質保証のプロフェッショナルチームの一員として、以下の業務に携わっていただきます。
    ■職務内容:GQP品質保証活動の実施、および既存の方針・手順、グローバル要件、政府規制に従って活動が行われることを確認
    GQP業務をサポートするための強固なローカル手順の確立と維持
    製造拠点と緊密に連携し、効果的で堅牢な品質システムと品質管理を確立
    製造拠点の逸脱、重大な調査、変更管理を担当し、業務および技術部門と強力に連携
    規制申請の更新や新製品の申請・発売に関連する変更管理活動をサポート
    製造拠点の定期的なGMP監査および監査ギャップの改善をサポート
    製造拠点の年間製品レビューの確認を支援
    新しい外部パートナーの事前承認のための品質デューデリジェンス評価を実施
    日本薬局方やその他の規定更新に関連するコンプライアンス活動をサポート。新しい規制要件および規制通知要件(例:ニトロソアミン評価、代替試験など)に関連するコンプライアンス活動をサポート
    ビジネス開発契約に関連する品質活動をサポートし、外部パートナーと連携
    規制当局との窓口役を務める場合があります
    販売承認ライセンスの更新のためのGQP規制査察をサポート
    販売監督総括者事務所、薬事部門、規制部門、国内外の製造拠点と連携し、GQP活動をサポートし、製品の安定供給を確保
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -022025-183806 Posted: 2025-04-22

    スペシャリスト

    GLP試験、信頼性基準の品質保証・監査業務のいずれかに従事された方必見です
    6 - 9.5 million yen Nara Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are a major Japanese pharmaceutical company. We are a pharmaceutical company focused on eye health in particular, and are engaged in the research, development, manufacturing, and marketing of pharmaceuticals in the ophthalmologic field. We are particularly strong in the treatment of dry eye, cataract, and glaucoma, and have earned trust for our high technology and quality. We also have operations around the world and aim to contribute to eye health from a global perspective. In research and development, we are active in introducing new treatments and technologies to meet the various needs related to vision.
    Responsibilities
    各種GXP監査業務を通じ、同社の各部門及び社外関連企業の業務の信頼性を保証・品質の向上を導き、同社の企業価値向上を図ります。非臨床監査責任者として、GLP試験の監査、信頼性基準に基づく監査業務を担っていただきます。担当する業務において、監査業務の課題解決に向けてリーダーシップを発揮しながら自律的に業務を遂行し、チーム運営の適正化・組織目標の達成に貢献いただきます。GLP省令、信頼性基準に基づいた各種非臨床監査試験の監査による品質・信頼性の保証
    製造販売承認申請資料監査による品質・信頼性の保証
    コンピュータ化システムの品質・信頼性の保証
    非臨床試験開発業務受託機関の事前評価・定期監査
    関連SOPの管理
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -022025-184458 Posted: 2025-04-22

    品質保証エンジニア

    医薬品・医療機器製造工場における品質部門での業務経験をお持ちの方必見です
    5 - 8 million yen - Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are the Japanese subsidiary of a healthcare product manufacturing and distribution company founded in the United States. Recognized as a workplace-friendly company in the healthcare industry, we offer a wide range of product lines. We supply various products necessary for surgeries and examinations to hospitals, care facilities, and other healthcare settings. The disposable nature of our products contributes to infection prevention and operational efficiency. With a focus on disposable surgical products, we provide a diverse range of offerings to meet the needs of our customers.
    Responsibilities
    製造所における薬機法・ISO13485等の要求事項に基づく品質マネジメントシステム全般の管理および維持改善
    リスクベースドに基づく品質傾向の分析、品質確保のための改善等の立案・実施
    クリーンルームやヒートシール等のプロセスバリデーション業務および関連プロジェクト業務の管理・実施
    サプライヤー、アウトソース先の管理
    社内外監査対応
    Risa Harada
    Risa Harada
    Medical Device
  • Job number: JN -012025-183167 Posted: 2025-04-22

    戦略企画担当者

    製薬企業におけるGxP業務経験をお持ちの方必見です
    6 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
    Responsibilities
    全社信頼性保証戦略の立案、パフォーマンスの把握と継続的改善
    信頼性保証ユニットにおける年度業績目標の立案、パフォーマンスの把握と推進
    信頼性保証ユニットDX戦略立案・推進
    Quality Culture醸成
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -032025-185317 Posted: 2025-04-22

    品質管理・品質保証業務(担当者)

    薬剤師免許保有者の方必見です。
    5.5 - 8.5 million yen Kanagawa Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are a company specializing in providing office equipment and solutions. In particular, we are widely known for our MFPs, printers, projectors, and other products that help improve the efficiency of the office environment. We also focus on providing cloud services and IT solutions to help our customers improve their business processes in an increasingly digital world. We are also actively involved in environmental protection, striving for sustainability through energy-efficient products and recycling programs.
    Responsibilities
    主に前臨床または治験用のmRNA原薬、およびそれらに関する治験薬等の製造指示書や品質管理試験の手順書等の文書確認
    GMP関連文書や種々の報告書等の記載内容の確認、妥当性検証
    GxP(主に治験薬GMP)関連文書の作成、教育、文書管理
    原材料等の供給元、外部委託先機関等のベンダー管理、GxP(主に治験薬GMP)工程で発生するイベント管理の自己点検、内外部の監査業務
    機器の適格性評価、バリデーション活動のサポート業務
    薬事調査・行政対応
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -012025-183429 Posted: 2025-04-22

    【東京/浮間研究所】品質保証担当者(生産技術本部)

    コーポレート品質保証部門としてのオペレーション業務をお任せ
    6 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
    Responsibilities

    ■仕事内容:当社の生産技術本部にて、GQP/GMP/QMS/GCTP/GDP等に基づくコーポレート品質保証部門としてのオペレーション業務をお任せ致します。
    開発品/市販品(バイオ原薬・無菌製剤および合成原薬・固形製剤)/医療機器/再生医療製品/コンビネーション製品等の技術/サイエンスに基づく製品品質評価(逸脱・変更などの品質イベントの科学的評価)
    国内外製造所/試験所の管理監督、品質改善支援、査察・監査マネジメント
    開発品の製品価値を創造する品質リーダー

    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -042025-186227 Posted: 2025-04-22

    品質戦略企画

    プロジェクトマネジメントのご経験をお持ちの方必見です
    7 - 10 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are a Japan-based pharmaceutical company dedicated to contributing to the health and well-being of patients worldwide. We have established a global network of research, development, manufacturing, and sales bases to achieve this mission. We focus particularly on areas with high unmet medical needs, such as "cognitive disorders and central nervous system diseases" and "oncology," striving to innovate and provide groundbreaking new drugs. Additionally, we work towards sustainable healthcare by fostering collaborative relationships with healthcare professionals, patients, and local communities.
    Responsibilities
    グローバルに跨る同社の製造所・製造委託先のグローバル事務局業務(品質委員会、変更管理、文書管理など)
    グローバルに跨るクオリティ関連のシステム(品質イベントシステムほか)導入などのデジタル化プロジェクト、スマートマニュファクチャリングの推進
    グローバルにおける品質向上プロジェクト推進(データインテグリティ、Good Distribution Practice: GDP)
    新製品導入プロジェクト推進
    その他規制要件対応、医薬品品質システムの構築、社内外関係部門との調整など
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -092024-176131 Posted: 2025-04-22

    【埼玉】原薬品質管理(QC)の機器・データ管理

    安定就業・有給休暇取得率77%
    7 - 10 million yen Saitama Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are committed to providing high-quality products and delivering appropriate safety information to patients and consumers worldwide. In our pharmaceutical business, we focus on developing anticancer drugs and other medications, offering treatments for cancer, immunology, allergies, and urology. Additionally, in our consumer healthcare business, we cultivate well-loved brands that contribute to the health and well-being of consumers over the long term.
    Responsibilities
    【オンコロジー領域に強み/安定就業・有給休暇取得率77%】
    ■業務内容:【変更の範囲:会社の定める業務】既存システムにおける機器・データ管理
    DX関連業務(デジタイゼーション/デジタライゼーションの推進,システム・機器の導入/改良,DX関連情報の収集など)
    分析関連機器のDIの推進
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -092024-176343 Posted: 2025-04-22

    バイオ医薬品原薬/中間体の品質保証業務

    残業月20h程・有給取得率90%◎/独身寮や社宅・50%会社負担借上げ制度有
    6 - 12.1 million yen Chiba Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are a leading comprehensive glass manufacturer in Japan. Our business extends beyond glass to include electronics, chemicals, and ceramics, resulting in a well-balanced revenue composition that makes us resilient even in economic downturns. We develop and manufacture innovative materials and products across a wide range of fields, leveraging our high technological expertise and research and development achievements. We supply products to various industries such as construction, automotive, electronics, and medical equipment. Furthermore, we are committed to environmental conservation and the development of sustainable technologies, earning us recognition as a socially responsible company.
    Responsibilities
    ■工場品質保証として、GMPの実務を実践していただきます。GMPオペレーションの実行と管理(例えば、変更管理、逸脱処置、文書管理、バリデーション、出荷管理、自己点検、供給者管理など)
    バリデーションの管理と実行(設備クオリフィケーション、プロセス・分析法・洗浄バリデーション、コンピュータ化システムの管理など)
    GMPシステムの構築(手順、SOPの策定など)。

    ■製造販売業者様との連携をとっていただきます。品質に関するコミュニケーション(変更や逸脱のご連絡、品質契約の締結など)
    新薬承認申請や、一部変更申請などの薬事的業務

    ■製造販売業者様の監査、医薬品規制当局の査察対応をしていただきます。
    ■海外関連会社とのGMPシステムのプラットフォームの共通化など、海外サイトとの協業をしていただきます。
    【当業務における魅力および留意点】お客様である製薬業者と技術提携し、恒常的に安定した医薬品を患者様へ供給する、社会的貢献が高い業務です。その中でも品質保証業務は、製造および品質管理を統括し、安定的な医薬品供給に責任を持つ業務であり、高い使命感を必要であり、業務達成満足度も高いものとなります。
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -102024-178677 Posted: 2025-04-22

    品質保証

    医薬品又は医薬部外品に関する品質保証業務のご経験者が活かせます。
    7 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    新薬とジェネリック医薬品の開発・製造・販売を行なっている製薬会社です。
    Responsibilities
    GQP業務全般(国内・海外製造所監査対応、CAPA管理、逸脱管理、変更管理、品質情報対応、取決め書の締結、市場出荷管理、教育訓練、文書管理、自己点検、査察対応など)
    薬事関連業務(GMP適合性調査申請、整合性調査など)
    部署運営業務
    Martin Tsvetkov
    Martin Tsvetkov
    Pharma
  • Job number: JN -122024-181262 Posted: 2025-04-22

    品質保証

    プロジェクトマネジメントの経験がある方必見です。
    5 - 8 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control

    Company overview
    We are the Japanese subsidiary of a healthcare product manufacturing and distribution company founded in the United States. Recognized as a workplace-friendly company in the healthcare industry, we offer a wide range of product lines. We supply various products necessary for surgeries and examinations to hospitals, care facilities, and other healthcare settings. The disposable nature of our products contributes to infection prevention and operational efficiency. With a focus on disposable surgical products, we provide a diverse range of offerings to meet the needs of our customers.
    Responsibilities
    国内外で製造される医療機器等の有効性、品質および安全性の確保新製品・変更品導入に関わる品質関連タスクの実施・進行(変更管理案件の場合)
    ディスコン手続き(品目・製造所・品番)
    試験サンプル手配、各種バリデーションレビュー、包装アグリメント更新、滅菌テスト手配、滅菌アグリメント更新、カタログ・案内文レビュー、QAD薬事データメンテナンス
    上記のための海外ベンダーとのコミュニケーション
    既存品における不適合や苦情発生対応、不具合による被害拡大防止・品質改善
    薬機法・ISO13485で求められる文書等を管理し、業態等維持
    その他:問合せ、請求書処理、監査の実施、その他プロジェクト
    Risa Harada
    Risa Harada
    Medical Device
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