Schnelle Bewerbung
2476
Erscheinungsdatum
Home-Office-Optionen
Pendelzeit
Bewerbungsart
Sprache
Fähigkeiten
Berufsfeld
Branche
Region
Städte
Berufserfahrung
Anstellungsart
Arbeitszeit
Filter
SortierungRelevanz
Beliebte Jobs
- Leitung Business Process Management
- Leitung Werkstatt
- Minijob
- Physiotherapeut Ausbildung
- Industriekaufmann Ausbildung
- Vertrieb
- Logopädie Ausbildung
- Kommunikation
- Werkstudent
- Rettungssanitäter Ausbildung
- Aushilfe
- Kfz Mechaniker Ausbildung
- Heilpraktiker Ausbildung
- MFA Ausbildung
- English Speaking
- Einzelhandel
Standorte
- München
- Augsburg
- Garching bei München
- Landsberg am Lech
- Starnberg
- Freising
- Ismaning
- Dachau
- Geretsried
- Unterschleißheim
- Erding
- Pfaffenhofen an der Ilm
- Unterföhring
- Aschheim
- Penzberg
- Ottobrunn
- Taufkirchen
- Gilching
- Gräfelfing
- Buchloe
- Europa
- Westliches Europa
- Süddeutschland
- Bayern
- Neckarland-Schwaben
- Südbayern
- Oberbayern
Home-Office-Optionen
Gehalt
Leg fest, wie viel du mindestens verdienen willst.
Pendelzeit
Bewerbungsart
Sprache
Fähigkeiten
Berufsfeld
Branche
Region
Städte
Berufserfahrung
Anstellungsart
Arbeitszeit
Beliebte Jobs
- Leitung Business Process Management
- Leitung Werkstatt
- Minijob
- Physiotherapeut Ausbildung
- Industriekaufmann Ausbildung
- Vertrieb
- Logopädie Ausbildung
- Kommunikation
- Werkstudent
- Rettungssanitäter Ausbildung
- Aushilfe
- Kfz Mechaniker Ausbildung
- Heilpraktiker Ausbildung
- MFA Ausbildung
- English Speaking
- Einzelhandel
Standorte
- München
- Augsburg
- Garching bei München
- Landsberg am Lech
- Starnberg
- Freising
- Ismaning
- Dachau
- Geretsried
- Unterschleißheim
- Erding
- Pfaffenhofen an der Ilm
- Unterföhring
- Aschheim
- Penzberg
- Ottobrunn
- Taufkirchen
- Gilching
- Gräfelfing
- Buchloe
- Europa
- Westliches Europa
- Süddeutschland
- Bayern
- Neckarland-Schwaben
- Südbayern
- Oberbayern
4.172 Treffer für Director Of Quality Management Jobs in Puchheim im Umkreis von 30 km
Noch nichts dabei? Es gibt 4172 weitere Jobs, die zu deiner Suche passen könnten
){kind=logo}
Schnelle Bewerbung
Zum nächstmöglichen Zeitpunkt suchen wir in Vollzeit sowie in unbefristeter Festanstellung einen Head of Quality - Automotive (w/m/d). * Du steuerst die Lieferantenqualität, die Kundenqualität, das Reklamationsmanagement und wirkst bei Bemusterungen und FMEA mit. * Du konzipierst, analysierst und bewertest aussagekräftige Qualitätskennzahlen und Reports und leitest daraus fundierte Entscheidungen sowie Verbesserungsinitiativen für Management und Fachbereiche ab. * Du unterstützt bei der Weiterentwicklung und Umsetzung des Integrierten Managementsystems (IMS), sowie bei der operativen Umsetzung von Normen und Standards, wie z.B. IATF 16949, ISO 9001, ISO 14001, TISAX. * Mehrjährige Berufs- und Führungserfahrung im Qualitätsmanagement eines Automotive-Produktionsumfelds (idealerweise Tier-1 oder OEM-nah) * Nachweisbare Erfahrung in der Anwendung produktionsnaher ...
Zum nächstmöglichen Zeitpunkt suchen wir in Vollzeit sowie in unbefristeter Festanstellung einen Head of Quality - Automotive (w/m/d). * Du steuerst die Lieferantenqualität, die Kundenqualität, das Reklamationsmanagement und wirkst bei Bemusterungen und FMEA mit. * Du konzipierst, analysierst und bewertest aussagekräftige Qualitätskennzahlen und Reports und leitest daraus fundierte Entscheidungen sowie Verbesserungsinitiativen für Management und Fachbereiche ab. * Du unterstützt bei der Weiterentwicklung und Umsetzung des Integrierten Managementsystems (IMS), sowie bei der operativen Umsetzung von Normen und Standards, wie z.B. IATF 16949, ISO 9001, ISO 14001, TISAX. * Mehrjährige Berufs- und Führungserfahrung im Qualitätsmanagement eines Automotive-Produktionsumfelds (idealerweise Tier-1 oder OEM-nah) * Nachweisbare Erfahrung in der Anwendung produktionsnaher ...
NEU
){kind=logo}
Senior Quality Manager CMO (m/f/x) Antibody Drug Conjugate (ADC) Manufacturing
Senior Quality Manager CMO (m/f/x) Antibody Drug Conjugate (ADC) Manufacturing
Daiichi Sankyo Europe GmbH
München
You will be responsible for managing quality oversight at CMOs, ensuring the implementation and maintenance of Daiichi Sankyo's quality standards (GMP/GDP) and regulatory requirements for our oncology products. o You are involved in establishment of new manufacturing processes and site transfer activities and act as quality supporting PPQ and validation activities - o At least two years in Quality Assurance and/or Quality Management, preferably in Shop Floor QA activities or QA Oversight for GMP operations - With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping ...
You will be responsible for managing quality oversight at CMOs, ensuring the implementation and maintenance of Daiichi Sankyo's quality standards (GMP/GDP) and regulatory requirements for our oncology products. o You are involved in establishment of new manufacturing processes and site transfer activities and act as quality supporting PPQ and validation activities - o At least two years in Quality Assurance and/or Quality Management, preferably in Shop Floor QA activities or QA Oversight for GMP operations - With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping ...
){kind=logo}
Director (gn) Portfolio Management, Market Analysis & Strategic Projects
Director (gn) Portfolio Management, Market Analysis & Strategic Projects
Formycon AG
Planegg
Teilweise Home-Office
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. We are looking for a Director (gn) Portfolio Management, Market Analysis & Strategic Projects with deep expertise in the global biosimilars market to drive strategic decision‑making at company level. * Preparation of strategic recommendations for the Board and Management * Translation of complex analyses into clear, management‑ready insights * Structured management of strategic, cross‑functional projects, ensuring alignment, transparency, and execution discipline * Several years of senior experience in portfolio management, strategy, market analysis, or corporate development, preferably within biosimilars and generics - With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain ...
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. We are looking for a Director (gn) Portfolio Management, Market Analysis & Strategic Projects with deep expertise in the global biosimilars market to drive strategic decision‑making at company level. * Preparation of strategic recommendations for the Board and Management * Translation of complex analyses into clear, management‑ready insights * Structured management of strategic, cross‑functional projects, ensuring alignment, transparency, and execution discipline * Several years of senior experience in portfolio management, strategy, market analysis, or corporate development, preferably within biosimilars and generics - With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain ...
Director (gn) Business Development - Licensing & Alliance Management
Director (gn) Business Development - Licensing & Alliance Management
Formycon AG
Planegg
Teilweise Home-Office
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. Reporting directly to the (CBO), the Director Licensing and Alliance Management is a key value driver for Formycon's external growth, portfolio monetization, and long‑term revenue generation. * Take full ownership of alliance management in late‑stage, launch, and post‑launch phases, ensuring strong profitability from existing partnerships and resolving execution challenges in advanced project stages - With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. Reporting directly to the (CBO), the Director Licensing and Alliance Management is a key value driver for Formycon's external growth, portfolio monetization, and long‑term revenue generation. * Take full ownership of alliance management in late‑stage, launch, and post‑launch phases, ensuring strong profitability from existing partnerships and resolving execution challenges in advanced project stages - With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.
){kind=logo}
Senior Product Manager - Materials Management (d/f/m)
Senior Product Manager - Materials Management (d/f/m)
4flow
Berlin, Düsseldorf, Hamburg, Heidelberg, München, Rüsselsheim, Stuttgart
Teilweise Home-Office
At least 6 years of product management experience, ideally with a strong background in supply chain systems - 4flow software develops a range of global standard software products for logistics and transportation planning that can be applied across all industries. The integrated planning approach of our software products ranges from the long-term optimization of network structures to the short-term optimization of transportation capacity utilization. In addition, planning results can be combined with transportation processing and accounting for integrated transportation management. Here, you will work at the intersection of logistics, technology, and compliance, driving product discovery and delivery. * Lead product discovery and delivery for materials and inventory management solutions for our global supply chain clients.
At least 6 years of product management experience, ideally with a strong background in supply chain systems - 4flow software develops a range of global standard software products for logistics and transportation planning that can be applied across all industries. The integrated planning approach of our software products ranges from the long-term optimization of network structures to the short-term optimization of transportation capacity utilization. In addition, planning results can be combined with transportation processing and accounting for integrated transportation management. Here, you will work at the intersection of logistics, technology, and compliance, driving product discovery and delivery. * Lead product discovery and delivery for materials and inventory management solutions for our global supply chain clients.
){kind=logo}
Built on passion and commitment to our work, belief in our goals and a drive to succeed regardless of the challenges we face. The Head of EMEA Regional Marketing is responsible for driving revenue growth and market share for the Bipolar Discrete portfolio across the EMEA region by bridging global strategy with regional execution. * Lead execution of regional marketing campaigns or programs that drive brand awareness, demand, and customer engagement. Team & Stakeholder Management * Influence internal stakeholders across functions (e.g., sales, finance, product groups, operations, quality, others) * Strong knowledge of semiconductor markets, customers, their applications, and/or supply chains * Team player who embraces responsibility and wants to be part of a winning team * Flexible working hours and possibility of overtime reduction to maintain a Work-Life-Balance
Built on passion and commitment to our work, belief in our goals and a drive to succeed regardless of the challenges we face. The Head of EMEA Regional Marketing is responsible for driving revenue growth and market share for the Bipolar Discrete portfolio across the EMEA region by bridging global strategy with regional execution. * Lead execution of regional marketing campaigns or programs that drive brand awareness, demand, and customer engagement. Team & Stakeholder Management * Influence internal stakeholders across functions (e.g., sales, finance, product groups, operations, quality, others) * Strong knowledge of semiconductor markets, customers, their applications, and/or supply chains * Team player who embraces responsibility and wants to be part of a winning team * Flexible working hours and possibility of overtime reduction to maintain a Work-Life-Balance
Zur Verstärkung unseres Teams am Standort München suchen wir eine erfahrene und engagierte Führungspersönlichkeit, die als Head of Qualified Person Support (m/w/d) Regional Quality * Schnittstellenmanagement mit internen Abteilungen (z.B. Regulatory, Supply Chain, Technology Development) und externen Partnern * Umfangreiche Erfahrung im Prozessmanagement, in der Umsetzung von Qualitätsverbesserungen sowie im Umgang mit Audits und Inspektionen auf Leitungsebene
Zur Verstärkung unseres Teams am Standort München suchen wir eine erfahrene und engagierte Führungspersönlichkeit, die als Head of Qualified Person Support (m/w/d) Regional Quality * Schnittstellenmanagement mit internen Abteilungen (z.B. Regulatory, Supply Chain, Technology Development) und externen Partnern * Umfangreiche Erfahrung im Prozessmanagement, in der Umsetzung von Qualitätsverbesserungen sowie im Umgang mit Audits und Inspektionen auf Leitungsebene
){kind=logo}
Anschreiben nicht erforderlich
Vorbereitung und Präsentation von Entscheidungsgrundlagen für Management und Kunden * Mehrjährige Erfahrung im Bereich Customer Quality, Projektqualität oder Serienqualität (Automotive) * Kommunikationsstärke und sicheres Auftreten gegenüber Kunden und Management
Vorbereitung und Präsentation von Entscheidungsgrundlagen für Management und Kunden * Mehrjährige Erfahrung im Bereich Customer Quality, Projektqualität oder Serienqualität (Automotive) * Kommunikationsstärke und sicheres Auftreten gegenüber Kunden und Management
){kind=logo}
Associate Director Regulatory Affairs – Clinical Lead*
Associate Director Regulatory Affairs – Clinical Lead*
Immatics Biotechnologies GmbH
Tübingen, München, Home-Office
Teilweise Home-Office
We are currently seeking an Associate Director Regulatory Affairs – Clinical Lead* to strengthen our EU Regulatory team. In this role, you will take ownership of EU regulatory strategy and execution for innovative oncology biopharmaceutical programs, including ATMPs, across early and late-stage development. You will independently lead EU regulatory activities for assigned clinical programs and act as a of regulatory strategy and execution. * Lead the preparation and coordination of Scientific Advice and other Health Authority interactions, including briefing documents, responses to questions, and meeting follow-up. * Drive initial clinical trial application and its lifecycle management, including major Substantial Modifications, with a proactive and risk-based mindset. This includes preparation, review and maintaining documentation of clinical trial applications.
We are currently seeking an Associate Director Regulatory Affairs – Clinical Lead* to strengthen our EU Regulatory team. In this role, you will take ownership of EU regulatory strategy and execution for innovative oncology biopharmaceutical programs, including ATMPs, across early and late-stage development. You will independently lead EU regulatory activities for assigned clinical programs and act as a of regulatory strategy and execution. * Lead the preparation and coordination of Scientific Advice and other Health Authority interactions, including briefing documents, responses to questions, and meeting follow-up. * Drive initial clinical trial application and its lifecycle management, including major Substantial Modifications, with a proactive and risk-based mindset. This includes preparation, review and maintaining documentation of clinical trial applications.
){kind=logo}
Teamleiter Qualitätssicherung (m/w/d) für den Bereich After Sales und Markt
Teamleiter Qualitätssicherung (m/w/d) für den Bereich After Sales und Markt
meinestadt.de
München
Teilweise Home-Office
Erfahrung in der Qualitätssicherung und dem Reklamationsmanagement im internationalen Markt
Erfahrung in der Qualitätssicherung und dem Reklamationsmanagement im internationalen Markt
){kind=logo}
Teamleiter Qualitätssicherung (m/w/d) für den Bereich After Sales und Markt
Teamleiter Qualitätssicherung (m/w/d) für den Bereich After Sales und Markt
BAUER KOMPRESSOREN GmbH
München
Teilweise Home-Office
Schnelle Bewerbung
Erfahrung in der Qualitätssicherung und dem Reklamationsmanagement im internationalen Markt
Erfahrung in der Qualitätssicherung und dem Reklamationsmanagement im internationalen Markt
){kind=logo}
Expert (d/m/w) Hardware Evaluation, Testing & Quality Assurance
Expert (d/m/w) Hardware Evaluation, Testing & Quality Assurance
genua GmbH
Kirchheim bei München
Teilweise Home-Office
Als Expert für Hardware Evaluation, Testing & Quality Assurance sorgst du dafür, dass unsere Hardware zuverlässig, leistungsfähig und sicher funktioniert. Du analysierst komplexe Zusammenhänge, entwickelst Teststrategien weiter und bist eine zentrale Schnittstelle zwischen Entwicklung, Produktmanagement und Operations an unserem Standort Kirchheim bei München. * Du fungierst als Bindeglied zwischen Entwicklung, Produktmanagement, Operations und Projektmanagement * Mehrjährige Erfahrung im Bereich Hardware Testing, Evaluation oder Quality Assurance
Als Expert für Hardware Evaluation, Testing & Quality Assurance sorgst du dafür, dass unsere Hardware zuverlässig, leistungsfähig und sicher funktioniert. Du analysierst komplexe Zusammenhänge, entwickelst Teststrategien weiter und bist eine zentrale Schnittstelle zwischen Entwicklung, Produktmanagement und Operations an unserem Standort Kirchheim bei München. * Du fungierst als Bindeglied zwischen Entwicklung, Produktmanagement, Operations und Projektmanagement * Mehrjährige Erfahrung im Bereich Hardware Testing, Evaluation oder Quality Assurance
){kind=logo}
Principal Researcher (f/m/d) - Foundation and World Models on Structured Business Data
Principal Researcher (f/m/d) - Foundation and World Models on Structured Business Data
SAP SE
Garching bei München, DE, 85748
We're builders touching over 20 industries and 80% of global commerce, and we need your unique talents to help shape what's next. At SAP's Business AI Research, we are exploring the next frontier of AI methods on structured business data – graphs, tables, time series, and more. We collaborate with our existing applied research teams in creating novel benchmarks for business problems and the development of novel architectures and , with the goal to publish benchmarks and at scientific conferences and in the open-source community. We are working jointly with our to create ever better means of solving real business problems. Originally known for leadership in enterprise resource planning (ERP) software, SAP has evolved to become a market leader in end-to-end business application software and related services for database, analytics, intelligent technologies, and experience management.
We're builders touching over 20 industries and 80% of global commerce, and we need your unique talents to help shape what's next. At SAP's Business AI Research, we are exploring the next frontier of AI methods on structured business data – graphs, tables, time series, and more. We collaborate with our existing applied research teams in creating novel benchmarks for business problems and the development of novel architectures and , with the goal to publish benchmarks and at scientific conferences and in the open-source community. We are working jointly with our to create ever better means of solving real business problems. Originally known for leadership in enterprise resource planning (ERP) software, SAP has evolved to become a market leader in end-to-end business application software and related services for database, analytics, intelligent technologies, and experience management.
){kind=logo}
Technology Business Leader (Data Centres)
Technology Business Leader (Data Centres)
Arup Deutschland GmbH
Berlin, Frankfurt, München, Düsseldorf
Teilweise Home-Office
Lead the expansion of our Data Centre business in a critical European market. You will position Arup not just as a provider, but as the market leader and trusted advisor for high-quality, sustainable, and resilient data centre solutions. This is a career-defining opportunity to take full ownership of Arup's Data Centre business in Germany. You will have the autonomy to define the strategy, drive commercial growth, and a high-performing team in one of the most dynamic sectors of the built environment. You will move beyond project delivery to become the face of Arup in the German market, cultivating strategic relationships with major clients and identifying new avenues for value creation. You will be instrumental in integrating our local strengths with our global expertise, fostering a culture of innovation that attracts the best talent and secures the most prestigious commissions.
Lead the expansion of our Data Centre business in a critical European market. You will position Arup not just as a provider, but as the market leader and trusted advisor for high-quality, sustainable, and resilient data centre solutions. This is a career-defining opportunity to take full ownership of Arup's Data Centre business in Germany. You will have the autonomy to define the strategy, drive commercial growth, and a high-performing team in one of the most dynamic sectors of the built environment. You will move beyond project delivery to become the face of Arup in the German market, cultivating strategic relationships with major clients and identifying new avenues for value creation. You will be instrumental in integrating our local strengths with our global expertise, fostering a culture of innovation that attracts the best talent and secures the most prestigious commissions.
){kind=logo}
Associate Director Country Operations Management
Associate Director Country Operations Management
Alexion Pharma Germany GmbH
Germany - Munich
Teilweise Home-Office
Schnelle Bewerbung
The Associate Director Country Operations Management (AD COM) reports to the of Country Operations. The Associate Director Country Operations Management (AD COM) is responsible for day-to-day management of a dedicated functional group(s) within Country Operations Management local team, and is responsible for planning and utilization of resources, objective setting and performance development. * Leading and developing of the dedicated functional group within Country Operations Management at local level. * Development and performance management of direct reports, including implementation of development and training plan and regular coaching of the direct reports. * Contribute to the quality improvement of the study processes and other procedures through close partnership with DCQ at Country level * Minimum 8 ( 5 for LM of CRAs only) years of experience in ...
The Associate Director Country Operations Management (AD COM) reports to the of Country Operations. The Associate Director Country Operations Management (AD COM) is responsible for day-to-day management of a dedicated functional group(s) within Country Operations Management local team, and is responsible for planning and utilization of resources, objective setting and performance development. * Leading and developing of the dedicated functional group within Country Operations Management at local level. * Development and performance management of direct reports, including implementation of development and training plan and regular coaching of the direct reports. * Contribute to the quality improvement of the study processes and other procedures through close partnership with DCQ at Country level * Minimum 8 ( 5 for LM of CRAs only) years of experience in ...
){kind=logo}
Deep understanding of EU pharmacovigilance expectations (EU legislation, EU regulations/directives, and GVP Modules) and the ability to translate requirements into pragmatic, high-quality execution. Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact. As Deputy EU QPPV, you act as the designated back-up for the EU QPPV during periods of absence and provide day-to-day operational leadership within the EU QPPV Office. * Support critical PV oversight and approvals, including aggregate reports, Risk Management Plans, risk minimisation measures/materials, PASS, responses to regulatory authorities, and the Pharmacovigilance System Master File.
Deep understanding of EU pharmacovigilance expectations (EU legislation, EU regulations/directives, and GVP Modules) and the ability to translate requirements into pragmatic, high-quality execution. Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact. As Deputy EU QPPV, you act as the designated back-up for the EU QPPV during periods of absence and provide day-to-day operational leadership within the EU QPPV Office. * Support critical PV oversight and approvals, including aggregate reports, Risk Management Plans, risk minimisation measures/materials, PASS, responses to regulatory authorities, and the Pharmacovigilance System Master File.
){kind=logo}
As Director of Biometrics, you will lead the team responsible for the core biometric recognition technology behind the World project - especially iris and face recognition, and the systems that make these technologies reliable and secure at massive scale. World is building a real human network designed to accelerate people in the age of AI. We're one of the fastest-growing networks in tech. World has been featured on the cover of TIME Magazine, highlighted in Fast Company's Next 5 in Fintech, and explored in a Bloomberg deep dive. The AI & Biometrics team is building a biometric recognition system that delivers an unprecedented level of accuracy at a billion people scale. We use cutting-edge machine learning models deployed on custom hardware to enable high-quality image acquisition, identification, and fraud prevention, all while requiring minimal user interaction.
As Director of Biometrics, you will lead the team responsible for the core biometric recognition technology behind the World project - especially iris and face recognition, and the systems that make these technologies reliable and secure at massive scale. World is building a real human network designed to accelerate people in the age of AI. We're one of the fastest-growing networks in tech. World has been featured on the cover of TIME Magazine, highlighted in Fast Company's Next 5 in Fintech, and explored in a Bloomberg deep dive. The AI & Biometrics team is building a biometric recognition system that delivers an unprecedented level of accuracy at a billion people scale. We use cutting-edge machine learning models deployed on custom hardware to enable high-quality image acquisition, identification, and fraud prevention, all while requiring minimal user interaction.
){kind=logo}
In this versatile position, which combines design, strategy and creative project management, your focus will be on excellent design in all phases of the project. * You will be responsible for the quality of all workplace interiors projects in the Munich studio – and will also set standards in your own projects. As Design Director - Workplace Interiors (m/f/d), you will play a key role in our Munich studio. You will lead our design team, shape our creative culture and take design quality to a new level. Als Design Director - Workplace Interiors (m/w/d) spielst du eine Schlüsselrolle in unserem Münchner Studio. * As the central point of contact for clients, you will manage the design process, maintain close and trusting relationships, and ensure that your design vision exceeds the set goals. * You define the creative basis of a project – formulating goals, strategies and a clear ...
In this versatile position, which combines design, strategy and creative project management, your focus will be on excellent design in all phases of the project. * You will be responsible for the quality of all workplace interiors projects in the Munich studio – and will also set standards in your own projects. As Design Director - Workplace Interiors (m/f/d), you will play a key role in our Munich studio. You will lead our design team, shape our creative culture and take design quality to a new level. Als Design Director - Workplace Interiors (m/w/d) spielst du eine Schlüsselrolle in unserem Münchner Studio. * As the central point of contact for clients, you will manage the design process, maintain close and trusting relationships, and ensure that your design vision exceeds the set goals. * You define the creative basis of a project – formulating goals, strategies and a clear ...
){kind=logo}
Ensure the delivery of high-quality, customer-centric technology solutions in close partnership with Product, enabling sustainable growth and continuous innovation * You have a proven ability to define and execute technology strategies aligned with business goals * You have a track record of delivering scalable, secure, and high-quality systems * Build, scale, and continuously evolve the Technology organisation, including its structure, operating model, processes, governance, and external management * Drive company-wide enablement through the effective use of advanced technologies, digitalised processes, and the responsible adoption of AI and emerging technologies to create sustainable value at both strategic and operational levels * Ensure the reliability, security, scalability, and maintainability of all systems, while maintaining full compliance with relevant information security standards
Ensure the delivery of high-quality, customer-centric technology solutions in close partnership with Product, enabling sustainable growth and continuous innovation * You have a proven ability to define and execute technology strategies aligned with business goals * You have a track record of delivering scalable, secure, and high-quality systems * Build, scale, and continuously evolve the Technology organisation, including its structure, operating model, processes, governance, and external management * Drive company-wide enablement through the effective use of advanced technologies, digitalised processes, and the responsible adoption of AI and emerging technologies to create sustainable value at both strategic and operational levels * Ensure the reliability, security, scalability, and maintainability of all systems, while maintaining full compliance with relevant information security standards
Schnelle Bewerbung
Director of Medical Affairs provides scientific and medical leadership to establish a deep understanding of the medical landscape regarding relevant, rare amyloidoses, such as AL-A, and Alexion products. Director of Medical Affairs Amyloidosis makes strategic contributions to Alexion's activities in the field of rare amyloidoses. * Disciplinary leadership of the Amyloidosis Medical Affairs team and ensuring the team's objectives are achieved through the efficient management of all directly reporting to the position and the retention of talented employees through personal development support. * Acquisition of sufficient knowledge of current local regulations of the pharmaceutical industry and collaboration with the Regulatory Affairs department, Pharmacovigilance department, Quality Assurance, Legal, Commercial Department and all other company divisions
Director of Medical Affairs provides scientific and medical leadership to establish a deep understanding of the medical landscape regarding relevant, rare amyloidoses, such as AL-A, and Alexion products. Director of Medical Affairs Amyloidosis makes strategic contributions to Alexion's activities in the field of rare amyloidoses. * Disciplinary leadership of the Amyloidosis Medical Affairs team and ensuring the team's objectives are achieved through the efficient management of all directly reporting to the position and the retention of talented employees through personal development support. * Acquisition of sufficient knowledge of current local regulations of the pharmaceutical industry and collaboration with the Regulatory Affairs department, Pharmacovigilance department, Quality Assurance, Legal, Commercial Department and all other company divisions
){kind=logo}
Advise the company' internal processes, including its Board of Directors, board committees and disclosure committee, on matters of US securities laws. * Good knowledge of regulatory processes, corporate governance, legal entity management, and corporate documentation. * Be part of an international and collaborative legal environment in a fast growing, innovative business on the forefront of top quality engineering. With a track record of innovation, INNIO designs, manufactures and services high performance power systems under its Jenbacher and Waukesha brands. INNIO operates a global installed base across approximately 100 countries as of December 31, 2025, supported by a resilient, high margin services business that delivers long term, recurring revenues across the full equipment lifecycle. To support INNIO in regulatory compliance and corporate governance matter relating to its US stock ...
Advise the company' internal processes, including its Board of Directors, board committees and disclosure committee, on matters of US securities laws. * Good knowledge of regulatory processes, corporate governance, legal entity management, and corporate documentation. * Be part of an international and collaborative legal environment in a fast growing, innovative business on the forefront of top quality engineering. With a track record of innovation, INNIO designs, manufactures and services high performance power systems under its Jenbacher and Waukesha brands. INNIO operates a global installed base across approximately 100 countries as of December 31, 2025, supported by a resilient, high margin services business that delivers long term, recurring revenues across the full equipment lifecycle. To support INNIO in regulatory compliance and corporate governance matter relating to its US stock ...
){kind=logo}
In this role, the VP oversees the Directors of Clinical Monitoring in Europe and North America, ensuring operational excellence across all monitoring activities and the consistent delivery of high‑quality outcomes to sponsors while meeting expectations, timelines, and regulatory standards. The VP is also responsible for establishing and leading a new organizational unit dedicated to feasibility assessments and the development and management of a robust network of site partnerships, including oversight of site contracting processes. In addition, the position oversees the Director of Study Start-Up, providing strategic and operational leadership to the study start up group. * Serves as a leader, point of mentorship, and point of escalation for the DirectorsDirectors of Clinical Monitoring, and Director(s) of Study Start Up.
In this role, the VP oversees the Directors of Clinical Monitoring in Europe and North America, ensuring operational excellence across all monitoring activities and the consistent delivery of high‑quality outcomes to sponsors while meeting expectations, timelines, and regulatory standards. The VP is also responsible for establishing and leading a new organizational unit dedicated to feasibility assessments and the development and management of a robust network of site partnerships, including oversight of site contracting processes. In addition, the position oversees the Director of Study Start-Up, providing strategic and operational leadership to the study start up group. * Serves as a leader, point of mentorship, and point of escalation for the DirectorsDirectors of Clinical Monitoring, and Director(s) of Study Start Up.
){kind=logo}
Schnelle Bewerbung
PFASuiki is developing advanced electrochemical oxidation technology to enable true destruction of PFAS (“forever chemicals”) at source. This is a consultative, technical-commercial role, responsible for building a structured, high-quality pipeline and progressing opportunities through: initial engagement to full-scale deployment. You will work at the interface of clients, engineering, and market strategy, ensuring opportunities are both technically credible and commercially viable. * Strategic Qualification: Evaluate opportunities based on regulatory pressure, matrix complexity, and commercial likelihood of conversion. * Stakeholder Management: Act as the interface bridging the gap between on-site EHS managers, engineering firms (EPCs), and C-suite procurement. * Market Savvy: Strong understanding of regulatory-driven markets and the adoption of emerging green technologies.
PFASuiki is developing advanced electrochemical oxidation technology to enable true destruction of PFAS (“forever chemicals”) at source. This is a consultative, technical-commercial role, responsible for building a structured, high-quality pipeline and progressing opportunities through: initial engagement to full-scale deployment. You will work at the interface of clients, engineering, and market strategy, ensuring opportunities are both technically credible and commercially viable. * Strategic Qualification: Evaluate opportunities based on regulatory pressure, matrix complexity, and commercial likelihood of conversion. * Stakeholder Management: Act as the interface bridging the gap between on-site EHS managers, engineering firms (EPCs), and C-suite procurement. * Market Savvy: Strong understanding of regulatory-driven markets and the adoption of emerging green technologies.
){kind=logo}
As part of our Tier 1 Account Team, you will work with a leading Automotive Tier 1 to understand its vision and liaise with all relevant Business Lines to make this vision a reality. The Global Key Account Director (GKAM) has end‑to‑end ownership and full accountability for the global Schaeffler AG account. The GKAM represents the single point of ultimate accountability for revenue, profitability, growth, and long‑term strategic positioning of across all Schaeffler business units and regions. * Ensure achievement of short‑, mid‑, and long‑term financial objectives, including forecasting accuracy and pipeline robustness - Leadership & Organization of the Global Account Team * Lead a global, cross‑functional virtual team, including Business Lines, Marketing, FAE, Operations, Quality, and Supply Chain - Governance, Risk & Stakeholder Management
As part of our Tier 1 Account Team, you will work with a leading Automotive Tier 1 to understand its vision and liaise with all relevant Business Lines to make this vision a reality. The Global Key Account Director (GKAM) has end‑to‑end ownership and full accountability for the global Schaeffler AG account. The GKAM represents the single point of ultimate accountability for revenue, profitability, growth, and long‑term strategic positioning of across all Schaeffler business units and regions. * Ensure achievement of short‑, mid‑, and long‑term financial objectives, including forecasting accuracy and pipeline robustness - Leadership & Organization of the Global Account Team * Lead a global, cross‑functional virtual team, including Business Lines, Marketing, FAE, Operations, Quality, and Supply Chain - Governance, Risk & Stakeholder Management
NEU
Schnelle Bewerbung
The CSM will work closely with of Country Operations (HCO), and/or Associate Director Country Operations Manager (AD COM), to ensure adequate study resourcing. * Quality and timeliness of study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) for assigned study(ies). * Quality of monitoring oversight in the assigned study(ies) * Relationship management with the national coordinating investigator as applicable and coordination of country level engagement activities. * Training, supporting and advising Investigators and in study related matters, including Risk Based Quality Management (RBQM) principles. The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory requirements.
The CSM will work closely with of Country Operations (HCO), and/or Associate Director Country Operations Manager (AD COM), to ensure adequate study resourcing. * Quality and timeliness of study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) for assigned study(ies). * Quality of monitoring oversight in the assigned study(ies) * Relationship management with the national coordinating investigator as applicable and coordination of country level engagement activities. * Training, supporting and advising Investigators and in study related matters, including Risk Based Quality Management (RBQM) principles. The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory requirements.