External Affairs Management Stellenangebote

Job vor 3 Tagen bei Jobvector gefunden Sanofi- Aventis Deutschland GmbH

Life Scientist as Medical Lead (m/f/d)

• Berlin, 10785 Führungs-/ Leitungspositionen Homeoffice möglich [...] English required About the jobThe General Medicines Medical Team at Sanofi is a high-performing team of Medical leaders who are a trusted source of scientific and Medical information and shared insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health. We represent diverse experiences and backgrounds which strengthens our team and mirrors the healthcare communities we engage. We are an innovative global healthcare company with a focus on immunology that extends to innovation in diabetes and transplant medicine. Across different countries, our talented teams are determined to deliver a best-in-class customer experience using the best of digital, artificial intelligence and personal know-how. With a focus on immunology that extends to innovation in diabetes and transplant medicines, we pursue progress to make a real impact on millions of patients around the world. The Transplant Medical Head GSA will lead the Medical and scientific (non-promotional) strategy for the GSA Transplant portfolio/ therapeutic area in close partnership [...] Leadership: Develop and execute the GSA Transplant Medical Roadmap, Medical Action Plan, and Evidence Generation Plan in close collaboration with internal stakeholders to align with global and local medical strategies. Cross-functional Collaboration: Work closely with various departments, including Brand, Public Affairs, and Global Medical teams, to ensure alignment on strategy, and coordinate with Field Medical teams to integrate office-and field-based activities effectively. Stakeholder Engagement: Build and maintain relationships with key opinion leaders, healthcare providers, academic institutions, and professional societies to foster partnerships, gain insights, and address challenges in patient care. Evidence Generation: Lead the design and execution of clinical trials, including Sanofi-sponsored and investigator-initiated studies, and collaborate with internal teams to generate data supporting the launch and lifecycle of transplant products. External Advisory Leadership: Conduct and lead external advisory boards focused on Sanofis transplant products and pipeline, ensuring engagement with key stakeholders and providing scientific education and updates on disease states and clinical trials. Team Management: Lead and mentor the GSA Transplant Medical team, including Medical Advisors and Field Medical Representatives, fostering a culture of collaboration, innovation, and continuous development. Medical Operations Oversight: Provide medical guidance for internal teams, ensuring the development of educational materials, presentations, and scientific communication strategies in support of product launches and ongoing medical education. Educational Background: Doctorate-level education (MD preferred) , PhD in Life Sciences, or PharmD. Minimum 5 years of experience in Medical Affairs, ideally within the relevant therapeutic area (Transplant, Hematology, or Oncology) . Leadership Experience: At least 3 years of experience managing teams, with the ability to travel up to 20-30 of the time. Subject Matter Expertise: Experience in Transplantation, either from academia/ research or the pharmaceutical industry, [...]
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Job vor 3 Tagen bei Jobvector gefunden Sanofi- Aventis Deutschland GmbH Medical Scientist as Medical Lead (m/f/d) • Berlin, 10785 Führungs-/ Leitungspositionen Homeoffice möglich [...] on millions of patients around the world. The Medical Head of Pediatric Vaccines assures the delivery and execution of the medical strategy, stakeholder engagement plan, and scientific activities, sharing medical expertise with internal stakeholders such as marketing, EbM/ HEOR, public affairs, communication, market access, clinical development, pharmacovigilance, and regulatory in compliance with law, ethical/ scientific principles, and group products strategy. The [...] and scientific (non-promotional) strategy for the German Pediatric Vaccines portfolio (RSV, Meningococcal Disease, PPH) in close partnership with the other functional franchise heads and in alignment with the overall franchise strategy Ensure high-quality delivery of scientific evidence to internal and external stakeholders Ensure subject safety by maintaining compliance with marketing authorization and promoting proper use of our products, particularly in communication [...] discipline Vaccines experience from academia/ research and/or preferably from the pharmaceutical industry with relevant customer knowledge Strong understanding of the German Healthcare system Skills:Strong business acumen to create compelling medical strategies benefiting patients, HCPs, and key external stakeholders Demonstrated team management capabilities Excellent interpersonal, communication, influencing, and networking skills with ability to work in cross-functional and multicultural teams Ability to manage [...]
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Job vor 6 Tagen bei Jobvector gefunden BioNTech SE

Oncologist as Director (m/f/d)

• Mainz, 55131 Führungs-/ Leitungspositionen Homeoffice möglich (Senior) Director, Clinical Development (m/w/d) London, United Kingdom; Berlin, Germany; Mainz, Germany full time Job ID:6950The Senior Director Clinical Development will work hand-in-hand with the[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] (e. g. Regulatory, Pharmacovigilance, Statistics, etc. ) and drives alignment on objectives and expected outcomes Responsible for study medical/ safety aspects and risk-benefit assessments supported by the study clinical expert and Pharmacovigilance. Collaborates closely with Pharmacovigilance on development of Risk Management Plans. Supervises ongoing medical data review and ensures medical queries of running studies are resolved Ensures at the program level, [...] complexity, as well as time and cost considerations Takes ownership together with partner functions in Development on the acceleration of program and trial design and innovation for the patient (e. g. digital endpoints, synthetic control arms, RWE/ HEOR, PRO, Medical Affairs) Owns and ensures preparation for clinical sections of key documents, including Investigators Brochures, IND summary documents, CTAs, responses to questions [...] regulatory authorities, IRBs and ethics committees, and NDAs. Oversees Clinical Study Report (CSR) medical content meets high quality expectations on medical standards, provides respective guidance to other members of the clinical development team Establishes, leads, and manages relationships with key external stakeholders (industry partners, Key Opinion Leaders, health authorities) . Represents the team to decision/ governance meetings, senior management, or advisory [...]
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Job vor 3 Tagen bei Mindmatch.ai gefunden STADA Arzneimittel AG Junior Specialist Regulatory Affairs Global Specialty/ Biosimilar Development (f/m/d) • Bad Vilbel Absolventen, Einsteiger, Trainees Jobticket [...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job vor 3 Tagen bei Mindmatch.ai gefunden STADA Arzneimittel AG

Junior Specialist for Regulatory Program Management/ IT systems (f/m/d)

• Bad Vilbel Absolventen, Einsteiger, Trainees Jobticket [...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]
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Job vor 3 Tagen bei Mindmatch.ai gefunden STADA Arzneimittel AG Pharmacist for Clinical Affairs Management (f/m/d) • Bad Vilbel Jobticket [...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]
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Job vor 3 Tagen bei Mindmatch.ai gefunden STADA Arzneimittel AG

Pharmaceutical Regulatory Affairs Junior Specialist-Global Development (f/m/d)

• Bad Vilbel Absolventen, Einsteiger, Trainees Jobticket Caring for Peoples Health as a Trusted Partner-This mission motivates us at STADA every day to improve the health of people worldwide. With our wide[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job vor 3 Tagen bei Mindmatch.ai gefunden STADA Arzneimittel AG Manager Clinical Affairs-Portfolio Product Development (f/m/d) • Bad Vilbel Jobticket [...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG

Project Manager Clinical Affairs EU (f/m/d)

• Hesse Jobticket [...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG Pharmacist for Clinical Affairs Management (f/m/d) • Hesse Jobticket Caring for Peoples Health as a Trusted Partner-This mission motivates us at STADA every day to improve the health of people worldwide. With our wide[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG

Junior Specialist Life Science/ Pharma Development (f/m/d)

• Hesse Absolventen, Einsteiger, Trainees Jobticket Caring for Peoples Health as a Trusted Partner-This mission motivates us at STADA every day to improve the health of people worldwide. With our wide[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG Junior Specialist for Regulatory Program Management/ IT systems (f/m/d) • Hesse Absolventen, Einsteiger, Trainees Jobticket Caring for Peoples Health as a Trusted Partner-This mission motivates us at STADA every day to improve the health of people worldwide. With our wide[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG

Manager Clinical Affairs-Scientific Evaluation (f/m/d)

• Hesse Jobticket [...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG Manager Clinical Affairs-Portfolio Product Development (f/m/d) • Hesse Jobticket [...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG Pharmaceutical Regulatory Affairs Junior Specialist-Global Development (f/m/d) • Hesse Absolventen, Einsteiger, Trainees Jobticket [...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG Pharmacist as Manager Clinical Affairs (f/m/d) • Hesse Jobticket Caring for Peoples Health as a Trusted Partner-This mission motivates us at STADA every day to improve the health of people worldwide. With our wide[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]

Job vor 5 Tagen bei JobMESH gefunden STADA Arzneimittel AG

Junior Specialist Regulatory Affairs Global Specialty/ Biosimilar Development (f/m/d)

• Hesse Absolventen, Einsteiger, Trainees Jobticket [...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job vor 10 Tagen bei Mindmatch.ai gefunden STADA Arzneimittel AG Junior Specialist Regulatory-Global Specialty Development (f/m/d) • Bad Vilbel Absolventen, Einsteiger, Trainees Jobticket Caring for Peoples Health as a Trusted Partner-This mission motivates us at STADA every day to improve the health of people worldwide. With our wide[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job vor 10 Tagen bei JobMESH gefunden STADA Arzneimittel AG

Manager Clinical Affairs (f/m/d)

• Hesse Jobticket [...] One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Manager Clinical Affairs (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development Professionals In your role as Manager Clinical Affairs, you will be responsible for the planning, preparation, and project management of clinical studies from phases I to IV, with a focus on bioequivalence studies. You will oversee the conduct of [...] to national and EU/ ICH law and ensure compliance with GCP standards. What you can expect: You will develop scientific evaluations and clinical study strategies. As a project manager, you will coordinate clinical studies and supervise contract research organizations and external partners. A key task of your responsibilities is the review of clinical study documents. As a clinical point of contact, [...]

Job vor 11 Tagen bei JobMESH gefunden STADA Arzneimittel AG Junior Specialist Regulatory-Global Specialty Development (f/m/d) • Hesse Absolventen, Einsteiger, Trainees Jobticket Caring for Peoples Health as a Trusted Partner-This mission motivates us at STADA every day to improve the health of people worldwide. With our wide[...]

MEHR INFOS ZUM STELLENANGEBOT

[...] want to become part of a dynamic, international team and grow with us? Then apply now as: Junior Specialist Regulatory-Global Specialty Development (f/m/d) Bad Vilbel Germany (DE) Full-time Permanent Portfolio Product Development What you can expect You support regulatory program management activities within global biosimilar and specialty projects. You contribute to the preparation and submission of Marketing Authorization Applications (MAAs) . [...] manage product information texts and coordinate translations across multiple markets. You prepare and publish eCTD sequences and handle documents using document management systems. You maintain regulatory data in internal databases and support xEVMPD submissions. You collaborate with internal stakeholders and external partners to ensure regulatory compliance. Whom we are looking for You hold a degree in life sciences or have completed [...] set clear priorities under tight timelines. You communicate clearly and proactively within cross-functional and international teams. You are fluent in English, both written and spoken; German or any additional language is a plus. You ideally bring first experience in Regulatory Affairs or knowledge of regulatory systems and databases. What we offer An open corporate culture with fast decision-making processes and a [...]

Job am 01.04.2025 bei Mindmatch.ai gefunden PAUL HARTMANN AG Manager Global Product Development (f/m/d) • Heidenheim, BW In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g.[...]

MEHR INFOS ZUM STELLENANGEBOT

In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g. suppliers, manufacturers) as well as internally (e. g. procurement) to our colleagues and be an expert [...] exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies with a focus on electrical engineering Development of new products in compliance with relevant regulations and standards Assist in technical design questions and support project management activities Set up electrical testing setups and collaborate with suppliers Technical responsibility for a dedicated product assortment in the field of negative pressure 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 [...]

Job am 01.04.2025 bei Mindmatch.ai gefunden PAUL HARTMANN AG Junior Product Developer-Global Product Development (f/m/d) • Heidenheim, BW Absolventen, Einsteiger, Trainees In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g.[...]

MEHR INFOS ZUM STELLENANGEBOT

In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g. suppliers, manufacturers) as well as internally (e. g. procurement) to our colleagues and be an expert [...] exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies with a focus on electrical engineering Development of new products in compliance with relevant regulations and standards Assist in technical design questions and support project management activities Set up electrical testing setups and collaborate with suppliers Technical responsibility for a dedicated product assortment in the field of negative pressure 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 [...]

Job am 01.04.2025 bei Mindmatch.ai gefunden PAUL HARTMANN AG Manager Global Product Development (f/m/d) - Medical Devices • Heidenheim, BW In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g.[...]

MEHR INFOS ZUM STELLENANGEBOT

In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g. suppliers, manufacturers) as well as internally (e. g. procurement) to our colleagues and be an expert [...] exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies with a focus on electrical engineering Development of new products in compliance with relevant regulations and standards Assist in technical design questions and support project management activities Set up electrical testing setups and collaborate with suppliers Technical responsibility for a dedicated product assortment in the field of negative pressure 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 [...]
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Job am 01.04.2025 bei Mindmatch.ai gefunden PAUL HARTMANN AG Ingenieur-Global Product Development (f/m/d) • Heidenheim, BW In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g.[...]

MEHR INFOS ZUM STELLENANGEBOT

In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g. suppliers, manufacturers) as well as internally (e. g. procurement) to our colleagues and be an expert [...] exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies with a focus on electrical engineering Development of new products in compliance with relevant regulations and standards Assist in technical design questions and support project management activities Set up electrical testing setups and collaborate with suppliers Technical responsibility for a dedicated product assortment in the field of negative pressure 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 [...]

Job am 04.01.2025 bei JobMESH gefunden PAUL HARTMANN AG Manager Global Product Development (f/m/d) • Baden- Württemberg In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g.[...]

MEHR INFOS ZUM STELLENANGEBOT

In this role you contribute to the development of our Wound Care portfolio. You will act as an interface to external service providers (e. g. suppliers, manufacturers) as well as internally (e. g. procurement) to our colleagues and be an expert [...] exciting phase full of energy awaits you. Responsibilities: Idea generation for new products and technologies with a focus on electrical engineering Development of new products in compliance with relevant regulations and standards Assist in technical design questions and support project management activities Set up electrical testing setups and collaborate with suppliers Technical responsibility for a dedicated product assortment in the field of negative pressure 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 [...]