58 Jobs für Surveillance Specialist
Stellenangebote Surveillance Specialist Jobs
Job am 14.11.2025 bei Mindmatch.ai gefunden
MED- EL
• AT- 7 Innsbruck
Abgeschlossenes Studium
Flexible Arbeitszeiten
Vigilance/ Post-Market
Surveillance Specialist (m/w/d) Ihre Aufgaben: Durchführung von Post-Market-Surveillance- und Vigilanz-Aktivitäten gemäß internen Verfahren und geltenden regulatorischen Anforderungen Koordination von Rückrufen und Maßnahmen im Feld sowie Aufbau und Pflege [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] qualitätsrelevanter Workflows, Prozesse und Verfahrensanweisungen Überwachung der Leistung und Sicherheit vermarkteter MED-EL Medizinprodukte, einschließlich Qualitätsdaten-Trendanalysen, Produktzuverlässigkeitsanalysen und [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Arthrex
Senior Vigilance Product Surveillance Specialist (w/m/d)
• Odelzhausen, Bavaria
Abgeschlossenes Studium
Flexible Arbeitszeiten Betriebliche Altersvorsorge
Ihre Aufgaben Sie sind verantwortlich für die Koordination, Erstellung und fristgerechte Abgabe von Vigilanz-Meldungen im Raum EMEA in Zusammenarbeit mit den Fachabteilungen Sie bewerten potenziell meldepflichtige Vorkommnisse Sie wirken bei [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der kontinuierlichen Optimierung der Abläufe und Prozesse im Reklamationsmanagement mit Sie erfassen und be [. .. ]
Job vor 3 Tagen bei JobMESH gefunden
Alber GmbH
• Baden- Württemberg 72458
Abgeschlossenes Studium
Work-Life-Balance
drive your life karriere bei alber Albstadt unbefristeter Vertrag Vollzeit ab sofort Compliance
Specialist EMEA (m/w/d) Deine Präzision, unser Antrieb. Deine Präzision, unser Antrieb. Mit großer Leidenschaft entwickeln wir bei [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Alber Produkte für Elektromobilität. Wir sind erfolgreich und wachsen, weil unsere Produkte für andere Menschen Freiheit und Selbstbestimmtheit im Alltag bedeuten. Wähle eine Aufgabe mit Sinn und werde Teil unseres Teams. Compliance [. .. ] Behandlung des Falls ein. Du unterstützt das Center of Excellence bei der Dokumentation nach MDR und Design History File (DHF) . Im Risikomanagement kümmerst du dich um die Post-Market Surveillance, um die Sicherheit und Konformität unserer Medizinprodukte auf dem Markt sicherzustellen. Du überwachst und analysierst Kundenbeschwerden, gewährleistest deren fristgerechte Bearbeitung und begleitest daraus resultierende Maßnahmen. Du unterstützt bei der Kommunikation mit zuständigen Behörden und benannten Stellen und arbeitest bei präventiven und korrektiven Maßnahmen eng mit ihnen zusammen. Deine Fähigkeiten Du [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job vor 4 Tagen bei Stellenanzeigen.de gefunden
GYNEMED GmbH Co. KG
• Schleswig- Holstein 23730
Homeoffice möglich
We are seeking an experienced and proactive Regulatory Affairs
Specialist to join our international team and strengthen our global regulatory and quality management activities. In this role, you will be [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] responsible for driving regulatory strategies and submissions not only in Europe (MDR) and the U. S. (FDA) , but also across diverse international markets. By ensuring compliance with global requirements [. .. ] and international agencies. Update, and maintain technical documentation and dossiers for medical devices (Class I to III) . Collaborate with quality management in risk assessments, usability analyses, and post-market surveillance. Maintain effective communication with global regulatory authorities, international partners, and internal teams. Your qualifications University degree in medical technology, natural sciences, quality engineering, or equivalent training with solid professional experience. Proven expertise in international regulatory approval procedures for medical devices (e. g. , Latin America, Middle East, Asia-Pacific, Canada, [. .. ]
Job vor 8 Tagen bei JobMESH gefunden
Alber GmbH
Compliance Specialist EMEA (m/w/d)
• Baden- Württemberg 72458 Albstadt
Abgeschlossenes Studium
Work-Life-Balance
drive your life karriere bei alber Albstadt unbefristeter Vertrag Vollzeit ab sofort Compliance
Specialist EMEA (m/w/d) Deine Präzision, unser Antrieb. Deine Präzision, unser Antrieb. Mit großer Leidenschaft entwickeln wir bei [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Alber Produkte für Elektromobilität. Wir sind erfolgreich und wachsen, weil unsere Produkte für andere Menschen Freiheit und Selbstbestimmtheit im Alltag bedeuten. Wähle eine Aufgabe mit Sinn und werde Teil unseres Teams. Compliance [. .. ] Behandlung des Falls ein. Du unterstützt das Center of Excellence bei der Dokumentation nach MDR und Design History File (DHF) . Im Risikomanagement kümmerst du dich um die Post-Market Surveillance, um die Sicherheit und Konformität unserer Medizinprodukte auf dem Markt sicherzustellen. Du überwachst und analysierst Kundenbeschwerden, gewährleistest deren fristgerechte Bearbeitung und begleitest daraus resultierende Maßnahmen. Du unterstützt bei der Kommunikation mit zuständigen Behörden und benannten Stellen und arbeitest bei präventiven und korrektiven Maßnahmen eng mit ihnen zusammen. Deine Fähigkeiten Du [. .. ]
Job am 14.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
• Bavaria 91719 Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job am 28.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Baden- Wurttemberg
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Paul Hartmann
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Bavaria Heidenheim
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d) At HARTMANN, were all in to help, care, protect and grow. We support healthcare professionals, that they can focus on what really matters: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to positively impact peoples life. We realize solutions that make a difference. And with your commitment you can [. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job vor 9 Tagen bei JobMESH gefunden
Alber GmbH
Compliance Specialist EMEA (m/w/d)
• Baden- Württemberg Albstadt
Abgeschlossenes Studium
Work-Life-Balance
Stellenangebot (https:/ / www. alber. de/ ) drive your life karriere bei alber Albstadt unbefristeter Vertrag Vollzeit ab sofort Compliance
Specialist EMEA (m/w/d) Deine Präzision, unser Antrieb. Deine Präzision, unser [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Antrieb. Mit großer Leidenschaft entwickeln wir bei Alber Produkte für Elektromobilität. Wir sind erfolgreich und wachsen, weil unsere Produkte für andere Menschen Freiheit und Selbstbestimmtheit im Alltag bedeuten. Wähle eine Aufgabe mit Sinn und werde Teil unseres Teams. Compliance [. .. ] Behandlung des Falls ein. Du unterstützt das Center of Excellence bei der Dokumentation nach MDR und Design History File (DHF) . Im Risikomanagement kümmerst du dich um die Post-Market Surveillance, um die Sicherheit und Konformität unserer Medizinprodukte auf dem Markt sicherzustellen. Du überwachst und analysierst Kundenbeschwerden, gewährleistest deren fristgerechte Bearbeitung und begleitest daraus resultierende Maßnahmen. Du unterstützt bei der Kommunikation mit zuständigen Behörden und benannten Stellen und arbeitest bei präventiven und korrektiven Maßnahmen eng mit ihnen zusammen. Deine Fähigkeiten Du [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
• Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Baden- Wurttemberg 89520 Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
• Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
Specialist in Regulatory affairs
• Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
Specialist Regulatory Affairs (m/w/d)
• Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
• Heidenheim
[. .. ] IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product [. .. ]
Job vor 9 Tagen bei Stellen-Online.de gefunden
Alber GmbH
Compliance Specialist EMEA (m/w/d) - Vollzeit
• Albstadt, 72458
Abgeschlossenes Studium
Work-Life-Balance
drive your life karriere bei alber Albstadt unbefristeter Vertrag Vollzeit ab sofort Compliance
Specialist EMEA (m/w/d) Deine Präzision, unser Antrieb. Deine Präzision, unser Antrieb. Mit großer Leidenschaft entwickeln wir [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] bei Alber Produkte für Elektromobilität. Wir sind erfolgreich und wachsen, weil unsere Produkte für andere Menschen Freiheit und Selbstbestimmtheit im Alltag bedeuten. Wähle eine Aufgabe mit Sinn und werde Teil unseres Teams. Compliance [. .. ] Behandlung des Falls ein. Du unterstützt das Center of Excellence bei der Dokumentation nach MDR und Design History File (DHF) . Im Risikomanagement kümmerst du dich um die Post-Market Surveillance, um die Sicherheit und Konformität unserer Medizinprodukte auf dem Markt sicherzustellen. Du überwachst und analysierst Kundenbeschwerden, gewährleistest deren fristgerechte Bearbeitung und begleitest daraus resultierende Maßnahmen. Du unterstützt bei der Kommunikation mit zuständigen Behörden und benannten Stellen und arbeitest bei präventiven und korrektiven Maßnahmen eng mit ihnen zusammen. Deine Fähigkeiten Du [. .. ]
Job am 15.11.2025 bei Mindmatch.ai gefunden
Ku Coin EU
• AT- 9 Wien
As part of Ku Coin EUs ongoing commitment to ensuring a secure and compliant trading environment, we are seeking an AML Operations
Specialist (f/m/d) to join our local Compliance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] function in Vienna. As an AML Operations Specialist, focusing on Transaction Monitoring Investigations, you will be responsible for detecting, investigating, and mitigating suspicious activity across Ku Coin EUs platform. You will focus on real-time transaction surveillance, applying analytical reasoning and data-driven insights to identify fraudulent or unusual behavior, mitigate risks, and maintain both platform integrity and user trust. You will work closely with our AML and Compliance teams to analyze on-chain and fiat transaction data, prepare reports for regulatory bodies, and strengthen our overall [. .. ]
Job am 04.11.2025 bei Mindmatch.ai gefunden
Abbott
Leadless Clinical Specialist (m/f/d) Cardiac Rhythm Management
• AT- 9 Wien
[. .. ] crisis-independent industry A company with flat hierarchies, open and appreciative communication, and a dynamic, highly skilled team A multinational environment that fosters talent development across the enterprise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Leadless Clinical Specialist (m/f/d) Cardiac Rhythm Management Location: Austria Purpose of the Role As a Leadless Clinical Specialist, you will serve as the field expert for Abbotts leadless cardiac technologies. You will provide procedural, technical, clinical, educational, and sales support to ensure the safe adoption and growth of leadless therapy. You [. .. ] range posted. JOB FAMILY: Support Services DIVISION: CRM Cardiac Rhythm Management LOCATION: Austria Vienna : Perfektastrasse 84-A ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 75 of the Time MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable J-18808-Ljbffr 68052168 [. .. ]
Job am 21.10.2025 bei Mindmatch.ai gefunden
Airborne Technologies GmbH
International Sales Developer (m/w/d)
• W wien
[. .. ] and systems engineering, developing innovative and flexible solutions tailored for governments, law enforcement, military, and various industries. Our expertise includes aircraft modifications and the integration of cutting-edge [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sensors for surveillance and reconnaissance applications. We are a passionate and dedicated team that thrives on innovation and excellence. If youre looking for more than just a job-if you want to contribute your skills to meaningful projects in an inspiring environment-youre in the right place with us. INTERNATIONAL SALES DEVELOPER (m/[. .. ] base. With a keen sense for market potential, you develop innovative strategies to achieve sustainable growth. Building and maintaining customer relationships: You establish long-term partnerships with key stakeholders in specialist organizations and governments through regular communication and personal meetings. Tailored solutions: You offer tailored solutions for each customer, after internal consultations with our technical department, making this role both diverse and demanding. Market analysis: Through continuous monitoring and evaluation of market and competitive developments, you identify relevant trends and opportunities, [. .. ]
Job am 05.09.2025 bei Mindmatch.ai gefunden
Airborne Technologies GmbH, Austria
International Sales Developer (m/w/d)
• AT- 3 Wiener Neustadt
[. .. ] and systems engineering, developing innovative and flexible solutions tailored for governments, law enforcement, military, and various industries. Our expertise includes aircraft modifications and the integration of cutting-edge [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sensors for surveillance and reconnaissance applications. We are a passionate and dedicated team that thrives on innovation and excellence. If youre looking for more than just a job-if you want to contribute your skills to meaningful projects in an inspiring environment-youre in the right place with us. Aufgaben Identification and acquisition [. .. ] base. With a keen sense for market potential, you develop innovative strategies to achieve sustainable growth. Building and maintaining customer relationships: You establish long-term partnerships with key stakeholders in specialist organizations and governments through regular communication and personal meetings. Tailored solutions: You offer tailored solutions for each customer, after internal consultations with our technical department, making this role both diverse and demanding. Market analysis: Through continuous monitoring and evaluation of market and competitive developments, you identify relevant trends and opportunities, [. .. ]
Job am 25.07.2025 bei Jobleads gefunden
Information Security Manager (all genders)
• Stuttgart, Baden- Württemberg
Sabbaticals Work-Life-Balance
[. .. ] and solution-oriented manner and are capable of driving topics forward proactively. You are a strong communicator and can convey complex topics appropriately to different audiences, including executive [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] management and specialist departments. You have business-fluent German skills and very good English skills. You demonstrate a high level of integrity, responsibility, and assertiveness. You enjoy shaping information security as a cross-functional topic and collaborating across departments. What We Have To Offer Discover new skills and improve your strengths, adapt your [. .. ] Business Continuity IT Security Manager (w/m/d) Information Security Risk Manager (m/w/d) Information Security Awareness Manager (m/w/d) Information Security Risk Manager (m/w/d) Construction Surveillance Technician-Build Lead Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 56263088 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Fachkraft für Abwassertechnik (m/w/d)
• München, Bayern
Homeoffice möglich
Flexible Arbeitszeiten Betriebliche Altersvorsorge Sabbaticals Jobticket 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] Internationally recognized for its innovative, competitive solutions, Ariane Group has expertise in all aspects of state-of-the-art space propulsion technologies. Ariane Group and its subsidiaries also offer their [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] specialist skills in space equipment, services, space surveillance, and critical infrastructure to benefit other industrial sectors. Equally owned by Airbus and Safran, the group employs more than 8, 000 highly qualified staff in France and Germany. Its 2022 revenues amounted to 2, 4 billion. #J-18808-Ljbffr 71744337 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Penetration Tester
• Essen, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten
[. .. ] and look forward to hearing from you. Spektrum supports apex purchasers (NATO, UN, EU, and National Government and Defence) and their Tier 1 supplier ecosystem with a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] wide range of specialist services. We provide our clients with professional services, specialised aerospace and defence sales, delivery, and operational subject matter expertise. We are looking for personnel to join our team and support key client projects. Who we are supporting The NATO Communication and Information Agency (NCIA) is responsible for providing secure and [. .. ] in the fields of capability delivery and service provision related to Consultation, Command Control as well as Communications, Information and Cyber Defence functions, thereby also facilitating the integration of Intelligence, Surveillance, Reconnaissance, Target Acquisition functions and their associated information exchange. The NCIA NATO Cyber Security Centre (NCSC) is responsible for planning and executing all lifecycle management activities for cyber security. In executing this responsibility, NCSC provides specialist cyber security-related services covering the spectrum of scientific, technical, acquisition, operations, maintenance, and [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Surveillance Specialist pro Jahr?
Als Surveillance Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Surveillance Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 58 offene Stellenanzeigen für Surveillance Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Surveillance Specialist Jobs?
Aktuell suchen 17 Unternehmen nach Bewerbern für Surveillance Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Surveillance Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Surveillance Specialist Stellenangebote:
- PAUL HARTMANN AG (10 Jobs)
- Alber GmbH (5 Jobs)
- GYNEMED GmbH Co. KG (2 Jobs)
- Airborne Technologies GmbH (2 Jobs)
- Stryker GmbH (2 Jobs)
- Jobijoba (2 Jobs)
In welchen Bundesländern werden die meisten Surveillance Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Surveillance Specialist Jobs werden derzeit in Baden-Württemberg (12 Jobs), Bayern (11 Jobs) und Hessen (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Surveillance Specialist Jobs?
Surveillance Specialist Jobs gehören zum Berufsfeld Polizei, Militär, Sicherheit.
