555 Jobs für External Affairs Management
Stellenangebote External Affairs Management Jobs
Job am 13.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 13.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Natural Scientist as Manager-Product Development Advanced Wound Care (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 13.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 13.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Manager Global Product Development (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 13.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Neu Job vor 4 Std. bei StepStone gefunden
Dr. Falk Pharma GmbH
Head of Global Medical Affairs (m/f/d)
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] by working together. That is why we are looking for: Falk Global Medical (GMED) bridges clinical development and commercial. We translate clinical science and communicate it externally [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and internally. GMED Affairs managers are working closely with their tandem GMED Science partners: Affairs focusing on the market, in permanent contact with HCPs, payers and patients, Science ensuring the solid scientific basis by contributing medical-scientific and compliance expertise. We are looking for a healthcare enthusiast and transformational leader who knows how to [. .. ] compelling medical story for appropriate audience Lead the medical TA strategy within their indication as well as integrated development teams Establish medical advisory boards and conduct regular meetings with key external experts Give input and participate in scientific events and international stand-alone symposia of the company Support the External Innovation, Development Partnering department through medical evaluation and due diligence support concerning potential pipeline candidates You will collaborate closely with Science Innovation, Falk Foundation, Market Access, Commercial as well as with [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Fresenius Kabi Deutschland GmbH
• Bad Homburg
[. .. ] to become part of our impressive growth story. To strengthen our team in the regulated (Gx P) environment, we are looking for a dedicated System Owner for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our global Regulatory Information Management System (RIMS) and the Electronic Common Technical Document (e CTD) as soon as possible. These systems are essential for the creation, management and submission of electronic marketing authorization documents in accordance with the e CTD standard. In this key role, you will assume overall responsibility for the entire life cycle of the [. .. ] in close collaboration with Quality Assurance and IT departments. Creation and maintenance of system documentation (SOPs, work instructions, system descriptions) . Serve as the main contact for specialist departments (Regulatory Affairs, QA, IT) and external service providers. Collaborate with interdisciplinary teams to define requirements and drive system acceptance. Manage incidents, changes, releases, and support audits and inspections. Degree in life sciences, computer science, or a related discipline Extensive experience working in regulated sectors such as Pharma, Biotech, or Med Tech Strong expertise in e CTD, regulatory [. .. ]
Job vor 3 Tagen bei StepStone gefunden
Mercedes- Benz Group AG
Praktikantin Leitungsstab External Affairs (Pflicht-Praktikum)
• Stuttgart
Homeoffice möglich
Flexible Arbeitszeiten
[. .. ] Stellennummer: MER0003V09 Sie interessieren sich für politische Themen und möchten hinter die Kulissen eines internationalen Automobilunternehmens blicken? Dann werden Sie Teil unseres Teams, unterstützen uns ab März [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 2026 im Bereich External Affairs und gestalten die politischen Angelegenheiten des Unternehmens aktiv mit. Wir als Team External Affairs streben durch den Aufbau und die Pflege guter Beziehungen zu den verschiedenen politischen Stakeholdern ein nachhaltiges Wachstum für die Mercedes-Benz Group AG an. Der Bereich unterstützt das Unternehmen auf allen Ebenen von lokalpolitischen Themen bis [. .. ] Korrespondenz Vorbereitung und Begleitung von politischen Besuchen und weiteren Terminen am Standort Die Tätigkeit kann ab März 2026 beginnen. Studiengang im Bereich der Internationalen Beziehungen, Politikwissenschaft, Volkswirtschaftslehre, Jura, Betriebswirtschaftslehre, Internationales Management, Wirtschaftsingenieurwesen, Wirtschaftsinformatik oder ein vergleichbarer Studiengang Sichere Deutsch- und Englischkenntnisse in Wort und Schrift Selbstständiges, strukturiertes Arbeiten und Zuverlässigkeit Kommunikative und organisatorische Fähigkeiten Analytische Denkweise, Affinität zu Zahlen und Wirkungszusammenhängen ist von Vorteil Sicherer Umgang mit MS Office, Kenntnisse bei der Nutzung von KI-Tools von Vorteil Umfassende Kenntnisse und [. .. ]
Job vor 5 Tagen bei StepStone gefunden
Testo Saveris GmbH
• Titisee- Neustadt bei Freiburg
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
[. .. ] die Zukunft der Testo Saveris Gmb H. The Regulatory Manager serves as the chief strategic authority for all regulatory matters within Testos Pharmaceutical Business Unit. This pivotal [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role moves beyond compliance management to actively shape the regulatory landscape and convert foresight into a competitive business advantage. You will ensure flawless global compliance across our innovative hardware, software, and service solutions while enabling strategic market access, accelerating product time-to-market, and reinforcing Testos reputation as a trusted, pioneering partner in the digital [. .. ] product lifecycle (Regulatory-by-Design) . Culture and Process: Establish, standardize, and maintain robust global internal regulatory processes and mandatory training to foster a strong, proactive culture of compliance. 3. External Influence and Thought Leadership Shape the Environment: Proactively build and nurture high-level relationships with global regulatory authorities and industry associations to strategically influence the direction of future Gx P and digital compliance standards relevant to Testos solutions. Thought Leadership Advocacy: Represent Testo in high-value regulatory working groups, consultation processes, [. .. ] and insight to the Strategic Account Management team to help close high-value, complex deals requiring deep regulatory validation. Deep Regulatory Expertise: Several years of progressive experience in pharmaceutical regulatory affairs or a quality function, with specific experience in international markets (including EMEA and US) and a proven ability to interpret and apply complex regulatory frameworks (FDA, EMA, IATA, WHO) . Technical Background: University degree in a technical or scientific field. Authority Engagement: Demonstrated experience in direct, successful engagement with regulatory [. .. ]
Job vor 5 Tagen bei StepStone gefunden
Elanco Animal Health GmbH
Senior Director-Head of Formulation Development SMTD (m/w/d)
• Monheim am Rhein
Führungs-/ Leitungspositionen
Jobticket
[. .. ] for Formulation Development within SMTD, aligning with Elancos pipeline objectives. Provide expert oversight and coaching for formulation development activities across numerous projects, ensuring timely achievement of milestones. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Collaborate with Regulatory Affairs, QA, and other cross-functional teams to ensure compliance with global regulatory requirements and commitments. What You Need to Succeed (minimum qualifications) : Education: Ph D (highly preferred) A minimum of 10 years of experience developing human or animal health products. Exceptional people and project leadership; Subject Matter Expert (SME) in [. .. ] change. Strong understanding of relevant regulations for product development and manufacturing requirements. Excellent verbal and written communication skills, with the ability to work effectively across all Elanco teams and with external collaborators. Additional Information: Location: Monheim, Germany Freedom for personal initiative and opportunities for individual further training Work in a dynamic team Subsidization of pension provision by the employer 40 hours/ week 30 days vacation Health and fitness offerings in an international company Subsidized Job Ticket and bike leasing Encourage individual [. .. ]
Job vor 11 Tagen bei StepStone gefunden
Mercedes- Benz AG
• Böblingen
Teilzeit Homeoffice möglich Werkstudenten
Flexible Arbeitszeiten
[. .. ] ist das Team Netzwerkentwicklung verantwortlich für die strategische Entwicklung der CKD-Standorte weltweit inkl. derer Produktportfolios. Dies erfolgt in enger Zusammenarbeit mit verschiedenen Schnittstellen. Hierzu gehören u. a. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] die Produktionsplanung, External Affairs, Controlling, Supply Chain und Sales. Neben der Integration von Prämissen in neue Produktprojekte, stehen die Wirtschaftlichkeitsbetrachtung sowie lokale Gesetzgebungen und aktuelle Entwicklungen der CKD Länder zu jeder Zeit im Fokus. Das bieten wir an: Kennenlernen der Abläufe eines DAX-Unternehmens Hautnah erleben, wie die internationale strategische Ausrichtung des Unternehmens erarbeitet [. .. ] zu: Unterstützung in der Abstimmung von entscheidungsrelevanten Prämissen und finanziellen Bewertungen in unterschiedlichen Projekten mit allen tangierten Projektpartnern aus Vertrieb, Controlling, Logistik, etc. Vorbereitung von Präsentationen und Entscheidungsvorlagen für das Management Mitwirken bei der Vor- und Nachbereitung von Meetings und Berichterstattung an das Management Organisation, Teilnahme und Mitarbeit an Projekt-Meetings mit teilweise internationalen Teilnehmern sowie direktem Kontakt zu unseren internationalen Produktionsstandorten Unterstützung bei der Identifikation und Bewertung von Komplexitätsindikatoren/-treibern und Ableitung eines Zielesystems im CKD Netzwerk Die Tätigkeit kann [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Engineer as Manager Regulatory Affairs-Quality Assurance (w/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
Job am 25.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Manager Regulatory Affairs Operations (w/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
Job am 14.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Engineer as Manager-Idea Generation/ Products Technologies (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 14.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Natural Scientist as Manager-Product Development Advanced Wound Care (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 14.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Manager-Innovation Development Wound Care (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 14.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Manager-Development Lifecycle Design Reviews (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job am 09.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Manager Global Product Development (f/m/d)
• Baden- Wurttemberg Heidenheim
[. .. ] Manager Global Product Development (f/m/d) DEU-Heidenheim In this role you contribute to the development of our Advanced Wound Care portfolio. You will act as an interface to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] external internal stakeholders and be an expert in the field of wound therapy. You will support our team, which drives the development of products with passion and dedication. If, like us at HARTMANN, you want to design products that make peoples lives better, we should definitely get to know each other-a dynamic and exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies Development of new products in compliance with relevant regulations and standards Management and leadership of projects throughout the development lifecycle including Design Reviews, Technical Reviews and Project Gate Reviews within the Innovation and Development areas of the Wound Management division Preparation and presentation of project status at all levels of the company Technical responsibility for a dedicated product assortment in the field of advanced wound care Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements Ensuring product compliance to all relevant rules and guidelines Qualifications: Completed studies in natural science/ engineering (e. g. medical technology, polymer science, chemistry) and the associated production technologies Experience in project collaboration and/or [. .. ]
Job vor 3 Tagen bei Stellenanzeigen.de gefunden
GYNEMED GmbH Co. KG
Regulatory Affairs Specialist (m/f/d) - Medical Devices (Full-time)
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will be 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 aligning closely with our quality management system, you will directly contribute to [. .. ] of working combined with a collaborative mindset. Fluency in German and English; additional languages are an advantage for international registrations. Confident communicator with the ability to build strong internal and external relationships. Proficiency in MS Office applications. We offer An exciting and varied role in a collaborative, international environment. Direct involvement in global registration strategies, with significant responsibility for markets outside the EU and U. S. Flat hierarchies and the opportunity to shape processes after structured onboarding. Attractive benefits in a [. .. ]
Job am 14.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Regulatory Affairs Manager-Risk Prevention/ Manufacturing Marketing (w/m/d)
• Bavaria 91719 Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
Job am 14.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Engineer as Manager Regulatory Affairs-Quality Assurance (w/m/d)
• Bavaria 91719 Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
Job am 14.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Bavaria 91719 Heidenheim
[. .. ] a difference. And with your commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Manager Regulatory Affairs Operations (w/m/d) DEU-Heidenheim Join HARTMANN and become part of a global team thats shaping the future of healthcare. As a Manager Regulatory Affairs Operations (f/m/d) we offer you a varied and challenging position in an international environment in the Division Risk Prevention. Here you can [. .. ] the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the 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 [. .. ] and management systems and associated processes Open and competent attitude when working with internal partners Strong communication skills with an open and professional attitude when collaborating with both internal and external partners IT affinity and proficiency with the MS Office package Fluent written and spoken German and English Benefits Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days paid leave per year, [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als External Affairs Management pro Jahr?
Als External Affairs Management verdient man zwischen EUR 70.000,- bis EUR 100.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für External Affairs Management Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 555 offene Stellenanzeigen für External Affairs Management Jobs.
Wieviele Unternehmen suchen nach Bewerbern für External Affairs Management Jobs?
Aktuell suchen 59 Unternehmen nach Bewerbern für External Affairs Management Jobs.
Welche Unternehmen suchen nach Bewerbern für External Affairs Management Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für External Affairs Management Stellenangebote:
- PAUL HARTMANN AG (70 Jobs)
- Discover International (11 Jobs)
- Bio Talent (11 Jobs)
- Paul Hartmann (8 Jobs)
- Jazz Pharmaceuticals (7 Jobs)
- United Nations (6 Jobs)
In welchen Bundesländern werden die meisten External Affairs Management Jobs angeboten?
Die meisten Stellenanzeigen für External Affairs Management Jobs werden derzeit in Bayern (113 Jobs), Berlin (40 Jobs) und Nordrhein-Westfalen (40 Jobs) angeboten.
Zu welchem Berufsfeld gehören External Affairs Management Jobs?
External Affairs Management Jobs gehören zum Berufsfeld Rechtswesen, Justiz und Verwaltung.
