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    • 東京23区, 東京都
    • permanent
    • ¥16,000,000 - ¥19,000,000 per year, 年収1,600 ~ 1,900万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Job Description:This position is the main Quality contact in Japan and will have strong experience in GxP’s, GQP and Quality Management Systems (QMS) and will have worked in an global Quality environment. This role will lead the implementation and execution of the local and Enterprise Quality System (SOP’s and Technology) and support compliance to current regulations, procedures and standards across the business.They will be a k
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Job Description:This position is the main Quality contact in Japan and will have strong experience in GxP’s, GQP and Quality Management Systems (QMS) and will have worked in an global Quality environment. This role will lead the implementation and execution of the local and Enterprise Quality System (SOP’s and Technology) and support compliance to current regulations, procedures and standards across the business.They will be a k
    • 東京23区, 東京都
    • permanent
    • ¥8,000,000 - ¥12,000,000 per year, 年収800 ~ 1,200万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容InnovationHigh unmet medical needsGrowing company求められる経験Desired Skills and Experiences:• 3 years+ experience in a quality assurance or quality control role, within pharmaceuticals or manufacture in the GMP/GQP area.• Experienced in supporting GMP audits and support of regulatory authority inspections in the different regions.• In-depth knowledge of GQP regulations • Lead QA performance in accordance with Japan regulations and SO
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容InnovationHigh unmet medical needsGrowing company求められる経験Desired Skills and Experiences:• 3 years+ experience in a quality assurance or quality control role, within pharmaceuticals or manufacture in the GMP/GQP area.• Experienced in supporting GMP audits and support of regulatory authority inspections in the different regions.• In-depth knowledge of GQP regulations • Lead QA performance in accordance with Japan regulations and SO
    • 東京23区, 東京都
    • permanent
    • ¥12,000,000 - ¥14,000,000 per year, 年収1,200 ~ 1,400万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Lead a dedicated team in ensuring top-tier quality standards for cutting-edge medical devices.Collaborate with global teams to drive innovation and continuous improvement in quality assurance practices.Take on a pivotal role with significant impact on patient safety and product excellence.求められる経験Experience & Skills:● Minimum of 5 years' experience in medical device quality assurance.● Experience as a General Supervisor with stro
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Lead a dedicated team in ensuring top-tier quality standards for cutting-edge medical devices.Collaborate with global teams to drive innovation and continuous improvement in quality assurance practices.Take on a pivotal role with significant impact on patient safety and product excellence.求められる経験Experience & Skills:● Minimum of 5 years' experience in medical device quality assurance.● Experience as a General Supervisor with stro
    • lisboa., lisboa
    • permanent
    A Randstad opera em Portugal e no Mundo como líder na área de recursos humanos em diversos setores. Em parceria com a Minsait an Indra Company, estamos a recrutar um quality assurance para a sua equipa na área da banca.Se consideras ser a pessoa ideal para abraçar este desafio, envia-nos a tua candidatura.
    A Randstad opera em Portugal e no Mundo como líder na área de recursos humanos em diversos setores. Em parceria com a Minsait an Indra Company, estamos a recrutar um quality assurance para a sua equipa na área da banca.Se consideras ser a pessoa ideal para abraçar este desafio, envia-nos a tua candidatura.
    • são paulo, são paulo
    • permanent
    Service description:Implement occupational safety policies and actions, document audits of third parties and providers, accident investigation, preparation and validation of occupational safety documentation, such as APR, PGR, Reports, identify deviations and propose technical solutions for risk situations. Monitor teams in the field, supervising and auditing compliance with security obligations; provide training, lectures and security dialogues. Work long
    Service description:Implement occupational safety policies and actions, document audits of third parties and providers, accident investigation, preparation and validation of occupational safety documentation, such as APR, PGR, Reports, identify deviations and propose technical solutions for risk situations. Monitor teams in the field, supervising and auditing compliance with security obligations; provide training, lectures and security dialogues. Work long
    • porto (full remote or hybrid), porto
    • permanent
    Randstad is recruiting 2 Quality Assurance Engineers (functional tester), for direct integration in a company located in the center of Porto.The work model can be full remote or hybrid (according to the candidate's preference).This professional will review and perform quality assurance and functionality testing of all aspects for the product releases focusing on software testing.
    Randstad is recruiting 2 Quality Assurance Engineers (functional tester), for direct integration in a company located in the center of Porto.The work model can be full remote or hybrid (according to the candidate's preference).This professional will review and perform quality assurance and functionality testing of all aspects for the product releases focusing on software testing.
    • 東京23区, 東京都
    • permanent
    • ¥10,000,000 - ¥12,000,000 per year, 年収1,000 ~ 1,200万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容主な職務内容:• 品質保証部門の運営、管理、メンバーの教育• GQP及びQMS体制の構築・運用及び生産管理/品質管理における品質保証体制の維持• GQP及びQMS監査(社内及び関連会社)の実施、社内外教育訓練の実施• 製品の品質情報に関する社内外関連責任者に対するタイムリーな報告• 監督官庁または管理当局への説明・交渉• 治験薬及び市販製品の品質保証の確保(出荷判定、品質情報処理、変更管理)• GQP及びQMS関連SOPのメンテナンス• 市販製品の品質クレーム対応(販売提携先との⼆次対応)• 製品回収の対応(Mock recallを含む)• 三役体制を構築するための総括責任者のサポート• 品質に関する問題発生時の総括責任者への報告及び改善に向けた社内関係者へのリーダーシップ(CAPA対応、)• その他信頼性保証体制の確⽴及びその運営業務を遂行するに当たり、以下のような社内関係部署と連携する役割を担います。• 日本の薬事責任者、安全管理責任者、開発責任者
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容主な職務内容:• 品質保証部門の運営、管理、メンバーの教育• GQP及びQMS体制の構築・運用及び生産管理/品質管理における品質保証体制の維持• GQP及びQMS監査(社内及び関連会社)の実施、社内外教育訓練の実施• 製品の品質情報に関する社内外関連責任者に対するタイムリーな報告• 監督官庁または管理当局への説明・交渉• 治験薬及び市販製品の品質保証の確保(出荷判定、品質情報処理、変更管理)• GQP及びQMS関連SOPのメンテナンス• 市販製品の品質クレーム対応(販売提携先との⼆次対応)• 製品回収の対応(Mock recallを含む)• 三役体制を構築するための総括責任者のサポート• 品質に関する問題発生時の総括責任者への報告及び改善に向けた社内関係者へのリーダーシップ(CAPA対応、)• その他信頼性保証体制の確⽴及びその運営業務を遂行するに当たり、以下のような社内関係部署と連携する役割を担います。• 日本の薬事責任者、安全管理責任者、開発責任者
    • södertälje, stockholms län
    • permanent
    Vi på Randstad Life Sciences söker nu dig som vill arbeta som QA-konsult hos oss med uppdrag hos AstraZeneca.Din rollOrganisatoriskt tillhör du en grupp om ca 30 personer som stödjer den sterila tillverkningen både i Snäckviken och i Gärtuna.Du arbetar nära den spännande och dynamiska produktionen och är med ”där det händer”. Dagligen deltar du i tvärfunktionella diskussioner vid produktionslinjen och tar avvägda beslut hur produktionen ska löpa vidare uti
    Vi på Randstad Life Sciences söker nu dig som vill arbeta som QA-konsult hos oss med uppdrag hos AstraZeneca.Din rollOrganisatoriskt tillhör du en grupp om ca 30 personer som stödjer den sterila tillverkningen både i Snäckviken och i Gärtuna.Du arbetar nära den spännande och dynamiska produktionen och är med ”där det händer”. Dagligen deltar du i tvärfunktionella diskussioner vid produktionslinjen och tar avvägda beslut hur produktionen ska löpa vidare uti
    • bengaluru, karnataka
    • permanent
    Coordinate IQAC Activities:Develop and implement an annual plan for IQAC activities in consultation with the IQAC committee.Organize and conduct meetings of the IQAC committee to discuss quality-related issues and formulate strategies for improvement.Documentation and Record Keeping:Maintain comprehensive documentation related to quality assurance, including meeting minutes, reports, and records of various initiatives undertaken.Ensure timely submission of
    Coordinate IQAC Activities:Develop and implement an annual plan for IQAC activities in consultation with the IQAC committee.Organize and conduct meetings of the IQAC committee to discuss quality-related issues and formulate strategies for improvement.Documentation and Record Keeping:Maintain comprehensive documentation related to quality assurance, including meeting minutes, reports, and records of various initiatives undertaken.Ensure timely submission of
    • 東京23区, 東京都
    • permanent
    • ¥7,000,000 - ¥11,000,000 per year, 年収700 ~ 1,100万円
    社名社名非公開職種品質保証、品質管理業務内容希少疾患領域新製品ローンチに携われる求められる経験•Strong hands-on GMP/GQP, New Product introduction, Quality Assurance / Compliance experience in pharmaceutical industry.•Exceptional Global communication and interpersonal skills, and ability to work globally in a matrix environment.•Business English level•Accountability and commitment for outcomes and project completion•Thorough knowledge of applicable local and global regulatory requirements required for Gx
    社名社名非公開職種品質保証、品質管理業務内容希少疾患領域新製品ローンチに携われる求められる経験•Strong hands-on GMP/GQP, New Product introduction, Quality Assurance / Compliance experience in pharmaceutical industry.•Exceptional Global communication and interpersonal skills, and ability to work globally in a matrix environment.•Business English level•Accountability and commitment for outcomes and project completion•Thorough knowledge of applicable local and global regulatory requirements required for Gx
    • tiszaújváros, borsod-abaúj-zemplén
    • permanent
    Cégleírás / Organisation/DepartmentTiszaújvárosi partnerünk részére keresünk gyártásközi ellenőr (MEO) kollégákat, akár azonnali kezdéssel!Pozíció leírása / Job descriptionA gyártott tételek minőségének folyamatos figyelemmel kíséréseTermékminták vizsgálataDöntés termék minőségérőlFélkész- és késztermékek ellenőrzéseElvárások / RequirementsA munkakör betöltésének feltételei: Első 3 hónapban 12 órás munkarend (2 nappal, 2 éjszaka, 4 nap pihenő),ezt követően
    Cégleírás / Organisation/DepartmentTiszaújvárosi partnerünk részére keresünk gyártásközi ellenőr (MEO) kollégákat, akár azonnali kezdéssel!Pozíció leírása / Job descriptionA gyártott tételek minőségének folyamatos figyelemmel kíséréseTermékminták vizsgálataDöntés termék minőségérőlFélkész- és késztermékek ellenőrzéseElvárások / RequirementsA munkakör betöltésének feltételei: Első 3 hónapban 12 órás munkarend (2 nappal, 2 éjszaka, 4 nap pihenő),ezt követően
    • 東京23区, 東京都
    • permanent
    • ¥5,000,000 - ¥9,000,000 per year, 年収500 ~ 900万円
    社名社名非公開職種品質保証、品質管理業務内容Support Local Operation Unit Manager in all Quality work related to the pro-jects being executed business unit of company. Ensure assurance support to the project management team in all quality related issues in the project to support project objective achievement in terms of quality, supplier & subcontractor quality, and customer satis-faction. Assuring and controlling Quality with systems, tools and teams to satisfy custom-er expect
    社名社名非公開職種品質保証、品質管理業務内容Support Local Operation Unit Manager in all Quality work related to the pro-jects being executed business unit of company. Ensure assurance support to the project management team in all quality related issues in the project to support project objective achievement in terms of quality, supplier & subcontractor quality, and customer satis-faction. Assuring and controlling Quality with systems, tools and teams to satisfy custom-er expect
    • 東京23区, 東京都
    • permanent
    • ¥8,000,000 - ¥12,000,000 per year, 年収800 ~ 1,200万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Responsibilities (include but are not limited to):•Act as back up for Quality Assurance Manager (Hinseki) •Collaborate with cross-functional departments to ensure timely implementation of quality processes•Release of Cell Therapy Finished Products in Japan and Quality monitoring of importation of Cell Therapy Finished Products in Japan when applicable•Maintain Standard Operating Procedures (SOPs) to ensure quality objectives are
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Responsibilities (include but are not limited to):•Act as back up for Quality Assurance Manager (Hinseki) •Collaborate with cross-functional departments to ensure timely implementation of quality processes•Release of Cell Therapy Finished Products in Japan and Quality monitoring of importation of Cell Therapy Finished Products in Japan when applicable•Maintain Standard Operating Procedures (SOPs) to ensure quality objectives are
    • 東京23区, 東京都
    • permanent
    • ¥4,000,000 - ¥6,200,000 per year, 年収400 ~ 620万円
    社名社名非公開職種品質管理・テスト・評価業務内容Hybrid WorkGood Work/Life balanceInternational Environment求められる経験●5 years of full stack development experience of B2B or B2C applications●Experience in consolidating data from multiple source systems●PHP and MySQL experience (Laravel)●Modern JavaScript (ES6+) and the experience with Vue, Nuxt, and Node●CSS and the inspiration/sense of turning designs to CSS●DRY code with automated tests and value readability and simplicity.●Excellen
    社名社名非公開職種品質管理・テスト・評価業務内容Hybrid WorkGood Work/Life balanceInternational Environment求められる経験●5 years of full stack development experience of B2B or B2C applications●Experience in consolidating data from multiple source systems●PHP and MySQL experience (Laravel)●Modern JavaScript (ES6+) and the experience with Vue, Nuxt, and Node●CSS and the inspiration/sense of turning designs to CSS●DRY code with automated tests and value readability and simplicity.●Excellen
    • gallarate, lombardia
    • permanent
    Randstad Talent Selection è la divisione specializzata nella ricerca e selezione di profili qualificati e con alta professionalità. Per la filiale italiana di una multinazionale tedesca del settore farmaceutico, selezioniamo un:Assistant Quality Assurance – Pharma
    Randstad Talent Selection è la divisione specializzata nella ricerca e selezione di profili qualificati e con alta professionalità. Per la filiale italiana di una multinazionale tedesca del settore farmaceutico, selezioniamo un:Assistant Quality Assurance – Pharma
    • singapore
    • permanent
    • S$4,600 - S$5,500 per month, AWS
    Operations PlannerAbout the company:My client is a specialized provider in the field of chemicals, offering groundbreaking products and services that cover a wide array of sustainable solutions. These encompass various sectors, including nutrition, health, safety, and the preservation of resources.Job Objective:Efficiently plan and schedule chemical food blend production with the local contract manufacturer, overseeing purchase orders and logistics coordin
    Operations PlannerAbout the company:My client is a specialized provider in the field of chemicals, offering groundbreaking products and services that cover a wide array of sustainable solutions. These encompass various sectors, including nutrition, health, safety, and the preservation of resources.Job Objective:Efficiently plan and schedule chemical food blend production with the local contract manufacturer, overseeing purchase orders and logistics coordin
    • herborn, hessen
    • permanent
    • €70,000 - €80,000 per year
    Sie haben Freude daran, die Produktqualität, das QM-System und interne Prozesse aktiv zu verbessern? Sie möchten Produktionsfreigabeverfahren erstellen und Produkte bei Reklamationen requalifizieren und die daraus resultierenden Abstellmaßnahmen entwickeln? Die Rolle soll im Rahmen einer dauerhaften Festanstellung bei unserem Mandanten am Standort Herborn (Hessen) zum nächstmöglichen Zeitpunkt besetzt werden. In Ihrer Position tragen Sie zur Sicherstellung
    Sie haben Freude daran, die Produktqualität, das QM-System und interne Prozesse aktiv zu verbessern? Sie möchten Produktionsfreigabeverfahren erstellen und Produkte bei Reklamationen requalifizieren und die daraus resultierenden Abstellmaßnahmen entwickeln? Die Rolle soll im Rahmen einer dauerhaften Festanstellung bei unserem Mandanten am Standort Herborn (Hessen) zum nächstmöglichen Zeitpunkt besetzt werden. In Ihrer Position tragen Sie zur Sicherstellung
    • kecskemét, bács-kiskun
    • permanent
    Cégleírás / Organisation/DepartmentPartnerünk egy nagy múltú, német központú autóipar gyártó cég. Néhány éve zöldmezős beruházásként jött létre jelenlegi telephelyük Kecskeméten, ahol jelenleg magas szintű automatizáltság mellett gyártanak fröccsöntött műanyag alkatrészeket és hővédő lemezeket. Ide keresik vevői minőségbiztosítási mérnök kollégájukat, aki tovább erősítené a minőségbiztosítási csapatukat.Pozíció leírása / Job descriptionA vevői minőségbizto
    Cégleírás / Organisation/DepartmentPartnerünk egy nagy múltú, német központú autóipar gyártó cég. Néhány éve zöldmezős beruházásként jött létre jelenlegi telephelyük Kecskeméten, ahol jelenleg magas szintű automatizáltság mellett gyártanak fröccsöntött műanyag alkatrészeket és hővédő lemezeket. Ide keresik vevői minőségbiztosítási mérnök kollégájukat, aki tovább erősítené a minőségbiztosítási csapatukat.Pozíció leírása / Job descriptionA vevői minőségbizto
    • são paulo, são paulo
    • permanent
    Randstad em parceria com AON contrataEstamos em busca de talentos incríveis para integrar a equipe de excelência da AON! Junte-se a nós!Na Aon, contribuímos para moldar decisões empresariais para melhor.Acreditamos que as empresas alcançam o sucesso quando as comunidades que atendem e as pessoas que empregam também prosperam.Trabalhamos lado a lado com nossos clientes, oferecendo aconselhamento e soluções que proporcionam clareza e confiança para que possa
    Randstad em parceria com AON contrataEstamos em busca de talentos incríveis para integrar a equipe de excelência da AON! Junte-se a nós!Na Aon, contribuímos para moldar decisões empresariais para melhor.Acreditamos que as empresas alcançam o sucesso quando as comunidades que atendem e as pessoas que empregam também prosperam.Trabalhamos lado a lado com nossos clientes, oferecendo aconselhamento e soluções que proporcionam clareza e confiança para que possa
    • 東京23区, 東京都
    • permanent
    • ¥10,000,000 - ¥13,000,000 per year, 年収1,000 ~ 1,300万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Have a direct impact on patient health & wellbeing.Emphasize employee growth & development.Work within a global facing environment.求められる経験● 3 years or more of experience in quality assurance or safety management in a medical device manufacturing company● Management experience● Proficiency in English (business level, capable of conducting phone/video conferences)保険健康保険 厚生年金保険 雇用保険休日休暇土曜日 日曜日 祝日給与年収1,000 ~ 1,300万円賞与2000000
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Have a direct impact on patient health & wellbeing.Emphasize employee growth & development.Work within a global facing environment.求められる経験● 3 years or more of experience in quality assurance or safety management in a medical device manufacturing company● Management experience● Proficiency in English (business level, capable of conducting phone/video conferences)保険健康保険 厚生年金保険 雇用保険休日休暇土曜日 日曜日 祝日給与年収1,000 ~ 1,300万円賞与2000000
    • herborn, hessen
    • permanent
    • €70,000 - €85,000 per year
    Sie möchten den strategischen Einkauf mit dem Fokus auf die Lieferantenauswahl und die Auditierung der Lieferantenprozesse unterstützen? Die Rolle soll im Rahmen einer dauerhaften Festanstellung bei unserem Mandanten am Standort Herborn (Hessen) zum nächstmöglichen Zeitpunkt besetzt werden. In Ihrer Position sind Sie zudem für die Bewertung der Lieferanten, das Lieferantenmonitoring und die Durchführung von Optimierungsmaßnahmen und Änderungsabwicklungen v
    Sie möchten den strategischen Einkauf mit dem Fokus auf die Lieferantenauswahl und die Auditierung der Lieferantenprozesse unterstützen? Die Rolle soll im Rahmen einer dauerhaften Festanstellung bei unserem Mandanten am Standort Herborn (Hessen) zum nächstmöglichen Zeitpunkt besetzt werden. In Ihrer Position sind Sie zudem für die Bewertung der Lieferanten, das Lieferantenmonitoring und die Durchführung von Optimierungsmaßnahmen und Änderungsabwicklungen v
    • 東京23区, 東京都
    • permanent
    • ¥7,000,000 - ¥8,000,000 per year, 年収700 ~ 800万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Opportunity to work in an innovative environment with cutting-edge IVD productsImpactful global reach, contributing to improving healthcare outcomes worldwideOpportunities for professional growth and career advancement in the IVD industry求められる経験Minimum Requirement● Licensed pharmacist ● +3 years of experienced in QA ● Business level Japanese / Conversational EnglishPreferred Requirement● Distinctive problem solving, organization
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容Opportunity to work in an innovative environment with cutting-edge IVD productsImpactful global reach, contributing to improving healthcare outcomes worldwideOpportunities for professional growth and career advancement in the IVD industry求められる経験Minimum Requirement● Licensed pharmacist ● +3 years of experienced in QA ● Business level Japanese / Conversational EnglishPreferred Requirement● Distinctive problem solving, organization
    • barcelona, cataluna
    • permanent
    - Elaboración de los PNTs- Colaboración con el Responsable del Área en la elaboración de las guías de fabricación, proponer mejoras y estandarización- Colaboración con el Responsable de Calidad en la cualificaciones de los equipos de planta de producción- Cumplimentación de la documentación de funcionamiento del ámbito (guías de fabricación, registros, etc.)- Control de procesos- Revisión de procesos de filtración y esterilización
    - Elaboración de los PNTs- Colaboración con el Responsable del Área en la elaboración de las guías de fabricación, proponer mejoras y estandarización- Colaboración con el Responsable de Calidad en la cualificaciones de los equipos de planta de producción- Cumplimentación de la documentación de funcionamiento del ámbito (guías de fabricación, registros, etc.)- Control de procesos- Revisión de procesos de filtración y esterilización
    • viladecáns, cataluna
    • permanent
    • €25,000 - €30,000 per year
    - Reportando a la Responsable de Garantía de Calidad, gestionar el sistema de calidad de la compañía.- Prospección continua del funcionamiento de la organización para detectar puntos débiles y realizar propuestas de mejora.- Gestión del sistema documental, del sistema CAPA y del sistema de Control de Cambios.- Soporte en auditorías para el mantenimiento de las certificaciones de calidad de la compañía.- Realización de auditorías internas y de auditorías a
    - Reportando a la Responsable de Garantía de Calidad, gestionar el sistema de calidad de la compañía.- Prospección continua del funcionamiento de la organización para detectar puntos débiles y realizar propuestas de mejora.- Gestión del sistema documental, del sistema CAPA y del sistema de Control de Cambios.- Soporte en auditorías para el mantenimiento de las certificaciones de calidad de la compañía.- Realización de auditorías internas y de auditorías a
    • 東京23区, 東京都
    • permanent
    • ¥9,000,000 - ¥10,000,000 per year, 年収900 ~ 1,000万円
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容職務範囲/職務責任・QMS規則に従い、品質マネジメントシステムを構築し、維持管理・薬機法に関する業許可の取得及び維持管理・薬事法、関連法規等に基づく規制遵守・安全管理および是正措置に関する意思決定職務(業務)内容・品質管理マネジメントの構築・維持・ 国内品質業務運営責任者業務・QMSおよびQMS組織の管理・マネジメントレビュー、QMS定例会の開催・QMSの研修記録を残す・QMS関連書類の保管・製造拠点を含むすべてのサプライヤーを対象とした年次評価。・製品標準書の作成・国内製造所の作業指示書の作成・QMSに関する全てのSOPを整備する・変更管理のための影響評価・リスクの評価と管理・品質のためのデータ分析・製品の市場リリースを担当・現場の安全に関する是正措置を講じる・年次監査と実地監査の両方に内部監査と外部監査に対応・PMDA、地方自治体との連携・ 本社監査オーガナイザー・安全管理部門の監督求められる経験【必須】・医療機器の品質管理部門での3年以上の経験・
    社名社名非公開職種安全性管理、品質保証、品質管理業務内容職務範囲/職務責任・QMS規則に従い、品質マネジメントシステムを構築し、維持管理・薬機法に関する業許可の取得及び維持管理・薬事法、関連法規等に基づく規制遵守・安全管理および是正措置に関する意思決定職務(業務)内容・品質管理マネジメントの構築・維持・ 国内品質業務運営責任者業務・QMSおよびQMS組織の管理・マネジメントレビュー、QMS定例会の開催・QMSの研修記録を残す・QMS関連書類の保管・製造拠点を含むすべてのサプライヤーを対象とした年次評価。・製品標準書の作成・国内製造所の作業指示書の作成・QMSに関する全てのSOPを整備する・変更管理のための影響評価・リスクの評価と管理・品質のためのデータ分析・製品の市場リリースを担当・現場の安全に関する是正措置を講じる・年次監査と実地監査の両方に内部監査と外部監査に対応・PMDA、地方自治体との連携・ 本社監査オーガナイザー・安全管理部門の監督求められる経験【必須】・医療機器の品質管理部門での3年以上の経験・
    • bristol, bristol
    • permanent
    • £60,000 - £65,000 per year
    Randstad C&P are currently recruiting for a Site Manager working for a regional business based in the Bristol area! The role is ideal for a Site Manager with a background in delivering commercial schemes, who is seeking to progress and develop in their career.Key Responsibilities:Oversee all on-site activities to ensure projects are delivered on time, within scope, and within budget.Manage and coordinate subcontractors, suppliers, and site staff to ensure
    Randstad C&P are currently recruiting for a Site Manager working for a regional business based in the Bristol area! The role is ideal for a Site Manager with a background in delivering commercial schemes, who is seeking to progress and develop in their career.Key Responsibilities:Oversee all on-site activities to ensure projects are delivered on time, within scope, and within budget.Manage and coordinate subcontractors, suppliers, and site staff to ensure
    • 東京23区, 東京都
    • permanent
    • ¥4,000,000 - ¥6,200,000 per year, 年収400 ~ 620万円
    社名社名非公開職種品質管理・テスト・評価業務内容Hybrid WorkGood Work/Life balanceInternational Environment求められる経験●BA/BS in Computer Science or related technical field or equivalent practical experience●4+ years of QA, Test, and related engineering experience of B2B or B2C solutions across multiple platforms (Web, Mobile application).●Capable of enagaing early in the product definition stage to start defining test cases, test plan and acceptance criteria.●Exhibited experience usin
    社名社名非公開職種品質管理・テスト・評価業務内容Hybrid WorkGood Work/Life balanceInternational Environment求められる経験●BA/BS in Computer Science or related technical field or equivalent practical experience●4+ years of QA, Test, and related engineering experience of B2B or B2C solutions across multiple platforms (Web, Mobile application).●Capable of enagaing early in the product definition stage to start defining test cases, test plan and acceptance criteria.●Exhibited experience usin
    • carpi, emilia romagna
    • permanent
    Randstad Talent Selection è la divisione specializzata nella Ricerca & Selezione di professionisti qualificati.Per azienda settore cartotecnico ricerca unQA SPECIALIST - SETTORE CARTOTECNICOsi offre: inserimento diretto in azienda a tempo indeterminato. Retribuzione e inquadramento saranno commisurati all'esperienza pregressa e alle competenze tecniche del candidato selezionato.orario di lavoro: dal lunedì al venerdì 9:00-13:00 e 14:00-18:00 con flessibili
    Randstad Talent Selection è la divisione specializzata nella Ricerca & Selezione di professionisti qualificati.Per azienda settore cartotecnico ricerca unQA SPECIALIST - SETTORE CARTOTECNICOsi offre: inserimento diretto in azienda a tempo indeterminato. Retribuzione e inquadramento saranno commisurati all'esperienza pregressa e alle competenze tecniche del candidato selezionato.orario di lavoro: dal lunedì al venerdì 9:00-13:00 e 14:00-18:00 con flessibili
    • bath, ontario
    • permanent
    One of our top partners in the Electric Vehicle space is preparing to build a facility that will be a crucial part of Canada’s Electric Vehicle (EV) supply chain in Kingston area.Our client is looking for a Customer QA Engineer who will be responsible for ensuring customer quality requirements, quality complaints and customer satisfaction.Advantages- Competitive salary- Health and Dental Benefits from day one- RRSP Match- Defined Contribution Pension Plan-
    One of our top partners in the Electric Vehicle space is preparing to build a facility that will be a crucial part of Canada’s Electric Vehicle (EV) supply chain in Kingston area.Our client is looking for a Customer QA Engineer who will be responsible for ensuring customer quality requirements, quality complaints and customer satisfaction.Advantages- Competitive salary- Health and Dental Benefits from day one- RRSP Match- Defined Contribution Pension Plan-
    • newbury, berkshire
    • permanent
    • £50,000 - £60,000 per year
    Randstad C&P are recruiting for a Senior Site Manager on behalf of a Tier One Contractor! The roles involves managing various schemes up to £10m ni value, generally working on refurbishment projects as well as some small extensions and conversions. The role is based in Newbury area, however involves an element of travel so candidates MUST have a Full UK Drivers Licence. The role has great perks in addition to a good salary, including an employee share sche
    Randstad C&P are recruiting for a Senior Site Manager on behalf of a Tier One Contractor! The roles involves managing various schemes up to £10m ni value, generally working on refurbishment projects as well as some small extensions and conversions. The role is based in Newbury area, however involves an element of travel so candidates MUST have a Full UK Drivers Licence. The role has great perks in addition to a good salary, including an employee share sche
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