problems, discovered in the assembly operations. - Promote and execute quality standards, inspection processes, and test methodology, quality plans, documents and reports. Assist in process certification
Ensure compliance with regulatory standards ISO 9001 and ISO 13485 Prepare reports and trend analysis related to quality data Lead investigations, close and track customer complaints and nonconformities
for Deviation/Investigation / CAPA ManagementPresent deviations during inspectionsGenerate KPIs, overviews and trend reports related to external deviationsSupports the qualification process of external
Fachliche Prüfung auf GMP-Compliance und Dossier-Konformität von Masterdokumenten von ProzessvalidierungsplänenDurchführung von Risikobewertungen und Reviews von Product Quality Reports (PQR)Pflege
market position, but also an exciting and dynamic working environment with flat hierarchies. Daily batch record approvals Ensure compliance with regulatory standards ISO 9001 and ISO 13485 Prepare reports
processes audits as a responsible lead auditor. Issuance of the audit report. Based on audit findings, controlling of necessary improvement measures and appropriate implementation, as well as the
processes audits as a responsible lead auditor. Issuance of the audit report. Based on audit findings, controlling of necessary improvement measures and appropriate implementation, as well as the
. Issuance of the audit report. Based on audit findings, controlling of necessary improvement measures and appropriate implementation, as well as the effectiveness measuring of corrective actions. If necessary
analyzes and report to management on quality issues and root causes of batteries. - Fulfillment of given targets and ensuring Quality Standards. Compliance with guidelines and other regulations and
, Virtualisierung, MonitoringPrüfen und freigeben von GMP Dokumenten (Lasten- / Pflichtenhefte, Risikoanalysen, Spezifikationen, Qualifizierungspläne / -Prüfpläne / -Reports) Berufserfahrung im pharmazeutischen
in SAP 8D Report Unterstützung bei der Einrichtung der Einführung von 5s Verfahren Das bringen Sie als Quality Assistant (m/w/d) mit: Sie haben eine abgeschlossene Ausbildung zum KFZ-Mechatroniker (m/w
planned quality activities performed. 10. Conduct Process Trainings. 11. Generate MSR covering all aspects or parameters of Project / Product Quality and report to the management 0. Qualifications
/Investigation / CAPA ManagementPresent deviations during inspectionsGenerate KPIs, overviews and trend reports related to external deviationsSupports the qualification process of external service and material
and propose requirements for technology transfers, process validation, cleaning validation, analytical methods validation, GDP, other CMC studiesReview and approve changes and reports (e.g. stability
* Preparation of Quality Reference Files before launch of the medicinal product * Risk Assessment for BOPPs * Preparation of risk assessments * Overview of submitted reports and planning of necessary
functionality of parts. Duties and Responsibilities: Coordinate, align and report on activities for Model Year and Running Change Measures. This includes the following: - Problem solving documentation
processes audits as a responsible lead auditor. Issuance of the audit report. Based on audit findings, controlling of necessary improvement measures and appropriate implementation, as well as the
trial parts, line support, part readiness (launch) reports (for management team), fixture and gauge concept(s), and capabilities validation. Identify critical supplier capacity/capability issues and
. - Analyze reports and returned product; recommends corrective action. - Investigate continual improvement processes. - Provide feedback to other departments as appropriate, to preclude future recurrences of
) Creation of reports on the current quality situation, development of relevant KPI's Assessment of existing data/processes and definition of necessary improvement projects or improvement measures
responsible lead auditor. Issuance of the audit report. Based on audit findings, controlling of necessary improvement measures and appropriate implementation, as well as the effectiveness measuring of
meetings with all stakeholders to ensure planned quality activities performed. 10. Conduct Process Trainings. 11. Generate MSR covering all aspects or parameters of Project / Product Quality and report to
/m/d) tätig Sie definieren und berichten Key Performance Indicators (KPIs) Sie führen Controlling und Reporting von Cost of Non Quality im Bereich Industry durch Sie erstellen Quality Reports
unit to better manage their businesses. Propose solution alternatives for agent coaching. Partner with BU management team to identify areas for improvement. Prepare regular audit reports and offer clear
mit einem ERP-System sowie in der Erstellung von Q-Reports fühlen Sie sich sicher Sehr gute Deutsch- und gute Englischkenntnisse runden Ihr Profil ab
transfers, process validation, cleaning validation, analytical methods validation, GDP, other CMC studiesReview and approve changes and reports (e.g. stability, qualification, validation)Writes and reviews
management team to identify areas for improvement. - Prepare regular audit reports and offer clear insights in work quality; Continually evaluate and develop audit/monitoring procedures to improve efficiency
Assurance - Crop Protection - part-time (20 hrs on 4 days a week) / permanent contract - Ref. No. 2021-15 Role and Responsibilities You will be responsible for audits of scientific reports in compliance with
und freigeben von GMP Dokumenten (Lasten- / Pflichtenhefte, Risikoanalysen, Spezifikationen, Qualifizierungspläne / -Prüfpläne / -Reports) Berufserfahrung im pharmazeutischen oder regulierten Umfeld
der Engineering Aktionen Fehleranalyse Aufbau von Key Performance Indikatoren für das NC Management Erstellen von Reports Einsteuerungen von Verbesserungen Mitwirken bei Verbesserungsmaßnahmen Ihr Profil
transfers, process validation, cleaning validation, analytical methods validation, GDP, other CMC studiesReview and approve changes and reports (e.g. stability, qualification, validation)Writes and reviews
-ordination and execution of processes audits as a responsible lead auditor. Issuance of the audit report. Based on audit findings, controlling of necessary improvement measures and appropriate implementation
Identify the supplier industrial risks and propose mitigation actions Initiate and manage supplier performance improvement projects Report on supplier operational performance Apply the current associated
incoming quality and functionality of parts. Essential Functions: - Coordinate, align and report on activities for Model Year and Running Change Measures. This includes the following: - Align withthe
Operations and / or Third Parties Collect, analyze and report metrics pertaining to GxP Compliance Unsere Anforderungen Bachelor’s degree preferable in a physical science, life science, pharmacy, business
Operations and / or Third Parties Collect, analyze and report metrics pertaining to GxP Compliance Bachelor’s degree preferable in a physical science, life science, pharmacy, business, engineering, or
and process development by using existing processes and methods. Coordinating the initial sample inspection activities with the customer, preparing the initial sample inspection report according to
, understanding and also creating of reports is required We offer you: Permanent employment contract Perspective to be taken over at our customer Salaries above the general pay scale and incentive
-ordination and execution of audits as a responsible lead auditor. Issuance of the audit report. Based on audit findings, controlling of necessary improvement measures and appropriate implementation, as well as
für diverse Dokumente und damit einhergehende Vorgänge aus dem Bereich der QCTransfer- und Validierungsprotokolle/-reports für Prüf-MethodenQualifizierungsprotokolle/-reports und Logbücher zu Kalibrierungen
teams from different business units and external partners Deliver reports on projects regarding time, quality, budget, changes, milestones and problems on a regular basis IT-Service-Management (Now 25
/Auditorenqualifikation zurückgreifen oder möchten in diesem Umfeld arbeiten * Sie verfügen über sehr gute Kenntnisse über gängige Qualitätsmanagementmethoden und -prozesse (PPAP, FMEA, 8D-Report, SixSigma) * Sie kennen