Stellenangebote für Regulatory Jobs in Fribourg Kanton

Top Job - Basel (Basel-Stadt) - F. Hoffmann-La Roche AG

Key external academic/commercial entities for collaborations on Real-World Data projects, setting up collaboration goals, and finalizing necessary legal and regulatory consideration for such a collaboration Contribute to regulatory submissions, Health Technology Assessments, Market Access

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Quality Engineer Regulatory (m/w) in der Schweiz (nahe Bodensee) Ihr Tätigkeitsbereich QMS/UMS Medizin-Anforderungen (ISO 13485, FDA, GMP, GDP) Interne und externe Audits KVP Projekte Verifikation und Validierung von Prozessen und Produkten (IQ, OQ, PQ) Qualitätsdatenerfassung

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Top Job - Zürich - Ernst & Young AG

Out both reactive and proactive data analysis of large volumes of unstructured and structured data. Working with clients, fraud investigators, internal and external auditors, lawyers and regulatory authorities in sensitive and sometimes adversarial situations. Working in our specialist forensic

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18.02.18 - Fribourg - New Work human resources SA

General. You are familiar with the relevant regulations and standards in the medical field (regulatory Requirements) as well as the ISO standard 13485 for medical devices. You are a detail- and result-oriented person who can inspire others. You show a high level of commitment and service orientation and

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14.02.18 - Bulle - 125.000 - 150.000

Demonstrated experience of - Quality Assurance, Quality Control or manufacturing fields - Demonstrated experience in audits and regulatory inspection preparation and execution including Pre-Approval Inspection and interactions with regulatory bodies. - Demonstrated ability to work

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14.02.18 - Bulle

Quality Assurance, Quality Control or manufacturing fieldsDemonstrated experience in audits and regulatory inspection preparation and execution including Pre-Approval Inspection and interactions with regulatory nstrated ability to work in a matrix

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11.02.18 - Fribourg - 80.000 - 100.000

Activities expected to bridge from legacy reporting " Supports execution of local Testing, Training and Cutover activities " Within above scope of responsibility operate according to internal standards, external au dit standards, regulatory standards and legal requirements Minimum requirements Eudcation

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09.02.18 - Fribourg

Spain, Denmark, and the United Kingdom " Design, implement, and revise as appropriate APLs import and export compliance processes including classification (e.g., HTS/HS/ECN); entry operations; regulatory import and reporting requirements; trade programs and agreements; valuation; export licensing and

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09.02.18 - Fribourg - 125.000 - 150.000

Spain, Denmark, and the United Kingdom " Design, implement, and revise as appropriate APLs import and export compliance processes including classification (e.g., HTS/HS/ECN); entry operations; regulatory import and reporting requirements; trade programs and agreements; valuation; export licensing and

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09.02.18 - Fribourg - 80.000 - 100.000

GCP QUALITY ASSURANCE MANAGER Votre mission Your mission ? ? Plan, prepare, perform report and present various GCP-related external and internal audits according to a pre-defined audit plan ? Ensure company's clinical and regulatory quality documents are defined, created, maintained and implemented

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09.02.18 - Ecublens (VD), Ecublens (FR) - 100.000 - 125.000

Sampling plan statistical definition statistical process control SPC Risk analysis FMEA failure mode and effect analysis . Minimum > industry is a major plus. Knowledge and application of

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05.02.18 - Fribourg - 100.000 - 125.000

High affinity to IT in general. - You are familiar with the relevant regulations and standards in the medical field (regulatory Requirements) as well as the ISO standard 13485 for medical devices. - You are a detail- and result-oriented person who can inspire others. - You show a high level of

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30.01.18 - Fribourg - 100.000 - 125.000

Appropriate APL's import and export compliance processes including classification (e.g., HTS/HS/ECN); entry operations; regulatory import and reporting requirements; trade programs and agreements; valuation; export licensing and reporting requirements; restricted party screening; anti-boycott - Manage customs

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Top Job - Meilen

Ihre Aufgaben · Fachliche und personelle Führung eines kleinen Teams · Planung und Koordination der Aktivitäten im Bereich Registrierung und Medical · Sicherstellung der Einhaltung von regulatorischen Anforderungen · Unterhalt, Erweiterung und Sicherstellung bestehender Produktzulassungen · Überwac

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Job Mission Lead and coordinate U.S. or E.U. submissions for manufacturing process changes and negotiate their approval Provide expertise on regulatory requirements and define the RA Strategy for SMO projects. Support submission activities for other High Volume Facilities (MSO, MJC) Ensure

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