Permanent

Spezialist für Qualitätssicherung

  • LocationWürzburg, Bayern, Germany
  • Salary€65000 - €75000 per annum
  • SectorCompliance
  • Job RefBH-86965
  • Contact
  • Published24 days ago

Übersicht

Ihre Aufgaben:
1. Entwicklung und Umsetzung von Qualitätssicherungsprozessen
2.  Mitverantwortung in der fachlichen Leitung des Qualitätssicherungsteams
3. Prozessoptimierung und Arbeitsablaufüberwachung
4. Unterstützung der Leitung Qualitätssicherung im Tagesgeschäft
5. Operative Mitarbeit in der Qualitätskontrolle

Ihr Profil:
1. Berufsausbildung, Meisterqualifikation oder Studium in den Bereichen Elektrik, Elektronik, Metall oder ähnlichem Bereich von Vorteil.
2. Idealerweise 2 Jahre Erfahrung in der Qualitätssicherung
3. Vorzugsweise Erfahrung im produzierenden Umfeld
4. Beurteilungs- und Analysevermögen, Führungsstärke, Teamfähigkeit

Wir bieten:
1. Zukunftsorientierter Arbeitsplatz in einem internationalen Technologieunternehmen
2. Individuelle Einarbeitung und Weiterbildungsmöglichkeiten
3. Attraktives Vergütungspaket und betriebliche Zusatzleistungen
4. Gute Erreichbarkeit mit kostenlosen Parkplätzen
5. Kostenlose Verpflegung und E-Bike-Leasing

Besuche unsere Website und unser LinkedIn-Profil für weitere Stellenangebote.

Wir respektieren Deine persönlichen Daten und würden sie niemals an Dritte weitergeben! Für weitere Informationen darüber, wie wir Deine Daten handhaben, kannst Du gerne unsere Datenschutzerklärung auf der Austin Fraser-Website überprüfen oder uns unter privacy@austinfraser.com kontaktieren.

Austin Fraser GmbH, Lenbachplatz 1, 80333 München Geschäftsführer: Peter Hart Handelsregister: HRB 200249 Sitz der Gesellschaft München
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Neue Stellen

    Manufacturing Quality Engineer

    UK

    Our client is a leading innovator in the design, development and manufacturing of medical devices, dedicated to improving patient outcomes and enhancing health-care delivery. The team are passionate professionals who are committed to developing cutting-edge solutions that make a difference in people's lives.

    Due to expansion of the team we have an exciting opportunity for a Manufacturing Quality Engineer to join the business. Key to this role will be someone with an Electronics Manufacturing background so although ISO13485 would be nice to have, we are also happy to consider other highly regulated industries if you have the necessary electronics experience as part of the role will be working on issues on the PCB’s to component level.

    You will have the choice of working 5 days a week or a condensed 4 day week with Fridays off! and the ideal candidate will have hands on experience in testing or investigation of PCB’s and working on non conformance's with testing/production/R&D. Report writing. Analysing data and offering solutions, amongst other things.

    You will be rewarded with fantastic benefits including:
    - 25 days' holiday pa, rising to 28, plus bank holidays
    - Pension Scheme
    - Bonus Scheme
    - Life assurance
    - Electric Car Benefit

    If this sounds of interest please apply ASAP as my client is currently shortlisting for interviews.

    Austin Fraser is committed to being an equal opportunities employer, and encourages applications from candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity status.

    Due to the volume of applications received, we are unable to provide individual feedback to unsuccessful applicants.

    Check us out on our website and LinkedIn for more roles.

    We respect your personal data and would never offer it to third parties! For more information on how we handle your data, feel free to check out the Austin Fraser Privacy Notice or contact privacy@austinfraser.com Austin Fraser International Ltd is registered in England: 14971372 Austin Fraser International Ltd, 33 Soho Square, London, W1D 3QU

    Regulatory Affairs Engineer

    UK

    Austin Vita are pleased to offer an exciting opportunity for a hands on Regulatory Engineer to join our client, an innovative medical device business who design, develop and manufacture a range of devices for global markets based in Buckinghamshire. This will be a site based role so suit someone who loves working in a Team and rolling up their sleeves to the broad range of tasks and challenges.

    The opportunity comes at a time of site expansion and natural growth within the Quality & Regulatory department, and your responsibilities will include:

    • Working with internal departments and external regulators, suppliers and customers with a broad remit to ensure the ongoing product and systems compliance to the applicable regulations and standards.
    • Assisting in the maintenance and review of technical product files and assist in the continued transfer to the MDR.
    • Working with the design department to ensure ongoing regulatory compliance of current and new products.
    • Collaborating with a team of design engineers to produce a variety of technical documentation (such as essential requirements, risk assessments, test reports, etc).
    • Producing documentation in compliance with the relevant regulatory standards.
    • Working with internal departments, Competent Authorities, other national authorities and our Notified Body on product and company registrations.
    • Working in conjunction with the Sales department to provide the necessary documentation to support the registration of our products in international territories.
    • Assisting in the actioning of regulatory requirements associated with NCRs, customer complaints, CAPA reports etc.

    To be successful in the role, we are looking for candidates with:
    • Relevant experience with MDD/MDR (essential).
    • Experience of interpreting and implementing standards and regulations.
    • Broad background in regulatory compliance of systems and products within a QMS.
    • Broad background in electro/mechanical products highly desirable, along with an understanding of the impact of regulatory requirements.
    • Experience of medical standards and European/ FDA regulations highly desirable.
    • Experience of medical device manufacturing and medical standards highly desirable.
    • Familiarity with translation/localisation processes may be useful.

    Qualifications:
    • Preferably degree educated in a technical subject, such as Engineering, or in a another subject with experience of technical industry.

    You will be rewarded with a great salary and benefits including company bonus, so if this sounds of interest please apply ASAP.

    Austin Fraser is committed to being an equal opportunities employer, and encourages applications from candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity status.

    Due to the volume of applications received, we are unable to provide individual feedback to unsuccessful applicants.

    Check us out on our website and LinkedIn for more roles.

    We respect your personal data and would never offer it to third parties! For more information on how we handle your data, feel free to check out the Austin Fraser Privacy Notice or contact privacy@austinfraser.com Austin Fraser International Ltd is registered in England: 14971372 Austin Fraser International Ltd, 33 Soho Square, London, W1D 3QU