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                          21 Treffer für Development Underwriter Jobs in Oberding im Umkreis von 30 km

                          Noch nichts dabei? Es gibt 21 weitere Jobs, die zu deiner Suche passen könnten

                          Quality Engineer (m/w/d) Aerospace

                          Blackwave GmbH
                          Taufkirchen
                          Teilweise Home-Office
                          Schnelle Bewerbung
                          We specialize in pushing boundaries through the development and production of high-performance, off-the-shelf pressure vessels and complex carbon structures. * Project & Process Quality Assurance: You define and implement quality assurance strategies across the entire product lifecycle - from suppliers and development to serial production. * Personal responsibility & creative freedom: You actively contribute to the further development of our production technologies. * Further development guaranteed: You will grow both professionally and personally through exciting projects and exchanges with .
                          We specialize in pushing boundaries through the development and production of high-performance, off-the-shelf pressure vessels and complex carbon structures. * Project & Process Quality Assurance: You define and implement quality assurance strategies across the entire product lifecycle - from suppliers and development to serial production. * Personal responsibility & creative freedom: You actively contribute to the further development of our production technologies. * Further development guaranteed: You will grow both professionally and personally through exciting projects and exchanges with .
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                          Consultant - quantitative Methoden & Strategy (w|m|d)

                          zeb
                          Berlin, Frankfurt, Hamburg, München, Münster
                          Teilweise Home-Office
                          Gemeinsam mit deinem persönlichen Career Development Councelor planst Du deinen individuellen Karrierepfad.
                          Gemeinsam mit deinem persönlichen Career Development Councelor planst Du deinen individuellen Karrierepfad.
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                          (Junior) IT Security Auditor (all gender)

                          usd AG
                          Bundesweit, Neu-Isenburg (Frankfurt a.M.), Köln, München
                          Teilweise Home-Office
                          Schnelle Bewerbung
                          Praktische Erfahrung rund um die Themen Identity & Access Management (IAM), Security Hardening, Secure Software Development, Network Security, Cloud Security Schwachstellenmanagement, Logging & Monitoring / Security Operations Center (SOC) und Security Incident Management
                          Praktische Erfahrung rund um die Themen Identity & Access Management (IAM), Security Hardening, Secure Software Development, Network Security, Cloud Security Schwachstellenmanagement, Logging & Monitoring / Security Operations Center (SOC) und Security Incident Management
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                          Quality Assurance Specialist for Quality Control (m/f/d)

                          Bavarian Nordic GmbH
                          Martinsried bei München
                          Teilweise Home-Office
                          We are a fully integrated vaccine company focused on the development, manufacturing, and commercialization of life-saving vaccines. We believe in creating an inclusive and flexible workplace with a strong focus on personal and professional development because we need each other to take things further.
                          We are a fully integrated vaccine company focused on the development, manufacturing, and commercialization of life-saving vaccines. We believe in creating an inclusive and flexible workplace with a strong focus on personal and professional development because we need each other to take things further.
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                          Compliance Monitoring and Implementation: Assist in the development, implementation, and monitoring of compliance policies and procedures, particularly in relation to sales partners and trade activities * Regulatory Research: Monitor and research relevant regulatory developments, including trade regulations, anti-bribery / anti-corruption laws, and industry standards * With regular, mutual, and appreciative feedback, we support you in your individual development and learn from you in the process
                          Compliance Monitoring and Implementation: Assist in the development, implementation, and monitoring of compliance policies and procedures, particularly in relation to sales partners and trade activities * Regulatory Research: Monitor and research relevant regulatory developments, including trade regulations, anti-bribery / anti-corruption laws, and industry standards * With regular, mutual, and appreciative feedback, we support you in your individual development and learn from you in the process
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                          Director of Programmes

                          European Southern Observatory (ESO)
                          Garching bei München
                          As a member of the ESO Directors' Team the Director of Programmes works closely with the and with the other Directors (both bi-laterally and as a team) in the development of overall policy and strategic planning across the Organisation. * Responsible for the development and implementation of programme-related strategies, plans, policies and practices. * Substantial experience with the development, construction or operation of astronomical facilities or comparable large research infrastructures. Evidence of continuing professional development, e.g. in leadership or management, will be an asset.
                          As a member of the ESO Directors' Team the Director of Programmes works closely with the and with the other Directors (both bi-laterally and as a team) in the development of overall policy and strategic planning across the Organisation. * Responsible for the development and implementation of programme-related strategies, plans, policies and practices. * Substantial experience with the development, construction or operation of astronomical facilities or comparable large research infrastructures. Evidence of continuing professional development, e.g. in leadership or management, will be an asset.
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                          As the project enters its next phase, our team is expanding to support the development of future services and products enabled by the IRIS2 system. As a member of an agile project organization, you will be expected to bring a flexible way of working and an adaptive mindset to a dynamic development environment.
                          As the project enters its next phase, our team is expanding to support the development of future services and products enabled by the IRIS2 system. As a member of an agile project organization, you will be expected to bring a flexible way of working and an adaptive mindset to a dynamic development environment.
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                          NEU
                          Our Clinical Development model brings the customer and the patient to the center of everything that we do. * Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. * Understands the monitoring strategy required for the study and, where required, participates in the development of the study risk assessment plan. * Provides feedback to on performance including strengths as well as areas for development. SummaryRoles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer ...
                          Our Clinical Development model brings the customer and the patient to the center of everything that we do. * Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. * Understands the monitoring strategy required for the study and, where required, participates in the development of the study risk assessment plan. * Provides feedback to on performance including strengths as well as areas for development. SummaryRoles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer ...
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                          You will contribute to the development of a professional customer management system and accompany quality control initiatives. You will help with the writing of reports, the development of presentations for management, and learning how to create meaningful analyses. Our client assignments will challenge you, and our experienced consulting team will actively support you so that you master significant challenges contributing to your personal development.
                          You will contribute to the development of a professional customer management system and accompany quality control initiatives. You will help with the writing of reports, the development of presentations for management, and learning how to create meaningful analyses. Our client assignments will challenge you, and our experienced consulting team will actively support you so that you master significant challenges contributing to your personal development.
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                          Participate in study start-up activities, including protocol development, investigator meetings, and regulatory submissions. * Provide medical input during study design, protocol development, and risk assessment to ensure scientific rigor and feasibility. * Contribute to the development of brochures, informed consent forms, and study-specific training materials.
                          Participate in study start-up activities, including protocol development, investigator meetings, and regulatory submissions. * Provide medical input during study design, protocol development, and risk assessment to ensure scientific rigor and feasibility. * Contribute to the development of brochures, informed consent forms, and study-specific training materials.
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                          In your role, you will be at the forefront of revolutionizing fusion energy, driving cutting-edge technology development and scientific breakthroughs. Your contributions will be crucial to the development of our demonstration facility in the US, advancing our operations, and solidifying our leadership in the fusion energy sector. * You will contribute to the further development of processes, such as oder-2-pay, risk management or supply chain activities
                          In your role, you will be at the forefront of revolutionizing fusion energy, driving cutting-edge technology development and scientific breakthroughs. Your contributions will be crucial to the development of our demonstration facility in the US, advancing our operations, and solidifying our leadership in the fusion energy sector. * You will contribute to the further development of processes, such as oder-2-pay, risk management or supply chain activities
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                          The Strategic Sourcing Manager (TPO) for Beckman Coulter Diagnostics is responsible for strategic sourcing, category and alliance management with Third-Party Organizations (TPO) to enable the successful development and commercialization of Beckman Coulter's diagnostic products. This includes, but is not limited to Supplier & Category Strategy, Strategic Supplier Identification & Evaluation, Alliance Management for Critical Partners, Complex Contract Negotiation & Management, Cross-Functional Partnership & Alignment, Risk Management & Mitigation, Cost Management & Value Engineering, Supplier Performance & Development, Market Intelligence & Trend Analysis and Compliance. * Strategic Sourcing: Develop and execute comprehensive sourcing strategies for Third-Party Organization (TPO) suppliers, components, sub-assemblies, and finished goods supporting new product development, launch and ...
                          The Strategic Sourcing Manager (TPO) for Beckman Coulter Diagnostics is responsible for strategic sourcing, category and alliance management with Third-Party Organizations (TPO) to enable the successful development and commercialization of Beckman Coulter's diagnostic products. This includes, but is not limited to Supplier & Category Strategy, Strategic Supplier Identification & Evaluation, Alliance Management for Critical Partners, Complex Contract Negotiation & Management, Cross-Functional Partnership & Alignment, Risk Management & Mitigation, Cost Management & Value Engineering, Supplier Performance & Development, Market Intelligence & Trend Analysis and Compliance. * Strategic Sourcing: Develop and execute comprehensive sourcing strategies for Third-Party Organization (TPO) suppliers, components, sub-assemblies, and finished goods supporting new product development, launch and ...
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                          8 passende Jobs liegen außerhalb deiner Region

                          Your expertise and judgment will be instrumental in guiding cross-functional teams, supporting innovation, and enabling successful product development and commercialization. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. * Lead and develop high-performing GCSP, Epidemiology, Medical Affairs, and Medical & Process Compliance teams, including people leadership, budgets, and talent development * Set and execute global Medical Affairs strategy aligned to development milestones, regulatory interactions, and commercialization plans; ensure medical accuracy and balance across all external scientific content
                          Your expertise and judgment will be instrumental in guiding cross-functional teams, supporting innovation, and enabling successful product development and commercialization. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. * Lead and develop high-performing GCSP, Epidemiology, Medical Affairs, and Medical & Process Compliance teams, including people leadership, budgets, and talent development * Set and execute global Medical Affairs strategy aligned to development milestones, regulatory interactions, and commercialization plans; ensure medical accuracy and balance across all external scientific content
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                          CMC Lead (m/f/d) is responsible for supporting the overall CMC strategies within projects, and manage for the development of small molecule pharmaceuticals. These project teams are cross functional teams based on the project needs and the respective development stage of the project. * Accountability to lead teams within overall CMC development project(s) * Drive strategies and activity within the team to support overall development plan. * Leads special project(s)/committee(s) that are critical to Compound development and/or Unit milestones. * Provides leadership in the project/development team as Matrix Lead for cross-functional working teams * At least 8+ years of experience in the pharmaceutical industry working in a small molecule drug development environment. * Extensive experience in project management, process, product, and/or analytical development activities and ...
                          CMC Lead (m/f/d) is responsible for supporting the overall CMC strategies within projects, and manage for the development of small molecule pharmaceuticals. These project teams are cross functional teams based on the project needs and the respective development stage of the project. * Accountability to lead teams within overall CMC development project(s) * Drive strategies and activity within the team to support overall development plan. * Leads special project(s)/committee(s) that are critical to Compound development and/or Unit milestones. * Provides leadership in the project/development team as Matrix Lead for cross-functional working teams * At least 8+ years of experience in the pharmaceutical industry working in a small molecule drug development environment. * Extensive experience in project management, process, product, and/or analytical development activities and ...
                          mehr
                          The Senior Tech Management Lead Drug Product is responsible for the development of the strategy and the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for investigational and commercial drugs to the sites of manufacture, both internal and external to Daiichi Sankyo, until transition to routine manufacture. * Lead and coordinate the Site-Launch activities and associated teams for internal and external sites and development projects * Multiple years of experience in the pharmaceutical/biotechnology industry working in a drug development environment * Extensive experience in CMC related functions including solid formulation and/or sterile and lyophilized process and product development * Excellent knowledge of CMC development, process development and technology transfer, CMC regulatory, and ...
                          The Senior Tech Management Lead Drug Product is responsible for the development of the strategy and the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for investigational and commercial drugs to the sites of manufacture, both internal and external to Daiichi Sankyo, until transition to routine manufacture. * Lead and coordinate the Site-Launch activities and associated teams for internal and external sites and development projects * Multiple years of experience in the pharmaceutical/biotechnology industry working in a drug development environment * Extensive experience in CMC related functions including solid formulation and/or sterile and lyophilized process and product development * Excellent knowledge of CMC development, process development and technology transfer, CMC regulatory, and ...
                          mehr
                          Schnelle Bewerbung
                          Die ectacom GmbH ist der führende Business Development Distributor (BDD) für anspruchsvolle Unternehmenslösungen im Bereich Business Continuity, IT Risk Management und Security. * Ein PAM arbeitet dabei interdisziplinär mit anderen Abteilungen, d.h. Business Development Management, Produktmanagement, Marketing sowie Technik zusammen.
                          Die ectacom GmbH ist der führende Business Development Distributor (BDD) für anspruchsvolle Unternehmenslösungen im Bereich Business Continuity, IT Risk Management und Security. * Ein PAM arbeitet dabei interdisziplinär mit anderen Abteilungen, d.h. Business Development Management, Produktmanagement, Marketing sowie Technik zusammen.
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                          Was ist das Durchschnittsgehalt für Development Underwriter in Oberding?

                          Durchschnittsgehalt pro Jahr
                          61.100 €

                          Das Durchschnittsgehalt für Development Underwriter in Oberding liegt bei 61.100 €. Gehälter für Development Underwriter in Oberding liegen im Bereich zwischen 53.100 € und 72.700 €.

                          Häufig gestellte Fragen

                          Wie viele offene Stellenangebote gibt es für Development Underwriter Jobs in Oberding?
                          Aktuell gibt es auf StepStone 21 offene Stellenanzeigen für Development Underwriter Jobs in Oberding.

                          Welche anderen Orte sind auch beliebt für Leute, die in Oberding einen Development Underwriter Job suchen?
                          Folgende Orte sind auch interessant für Leute, die in Oberding einen Development Underwriter Job suchen: München, Garching bei München, Gilching.

                          Welche anderen Jobs sind beliebt bei Kandidaten, die nach Development Underwriter Jobs in Oberding suchen?
                          Wer nach Development Underwriter Jobs in Oberding sucht, sucht häufig auch nach Consultant Project Management, Head of Project Management, Design Project Manager.

                          Welche Fähigkeiten braucht man für Development Underwriter Jobs in Oberding??
                          Für einen Development Underwriter Job in Oberding sind folgende Fähigkeiten von Vorteil: Risikomanagement, Kommunikation, Entwicklung, Führung, Projektkompetenz.

                          Zu welcher Branche gehören Development Underwriter Jobs in Oberding?
                          Development Underwriter Jobs in Oberding werden allgemein der Kategorie Versicherungen zugeordnet.

                          Wie viele offene Teilzeit-Stellen gibt es für Development Underwriter Jobs in Oberding?
                          Für Development Underwriter Jobs in Oberding gibt es aktuell 3 offene Teilzeitstellen.