Manager Product Documentation Stellenangebote


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Stellenangebot Manager Product Documentation Job bei Dedalus Health Care GmbH Job vor 2 Tagen gefunden Dedalus Health Care GmbH

Technical Product Manager (m/w/d) Frames

• Trier, Home- Office Homeoffice möglich Work-Life-Balance
MEHRProduct Management, Technical Product Manager, healthcare . Dedalus Health Care GmbH sucht in Trier, Home- Office eine/n Technical Product Manager (m/w/d) Frames (ID- Nummer: 11731854) [...] partners Analysis, prioritization and implementation of market and internal requirements and trends Conception and validation of development requirements in close cooperation with end- users, UX designers and development teams Functional guidance of the development team and adjacent areas such as documentation A successfully completed degree in the field of health care or engineering, alternatively an equivalent combination of education and professional [...]
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Job vor 10 Tagen gefunden Takeda GmbH Process Validation Engineer (f/m/d) • Singen
MEHR[...] CMO manufacturing site include, but are not limited to, the following areas. How you will contribute: Validation subject matter expert to conceive, design and direct the execution of validation/ technical shared services projects in support of VBU Authoring process validation documentation for Lifecycle Process Validation Oversight and approval of process validation activities, as well as perform data analysis and compilation of [...] and support and maintain the process validation communications board and community of practice Establish, support and direct collaborative projects with other VBU functions for example CMC, External Manufacturing, PO, Quality and External Partners CMOs to generate and execute process and product technology transfers and the associated qualification and validation activities In this position you will report to the Senior Manager, Vaccines MS T Validation. What you bring to Takeda: You have completed studies in the natural sciences field Several years [...]
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Job vom 28.10.2024 Takeda GmbH

Manager MS T Analytical Lab (f/m/d)

• Singen
MEHR[...] is true to the best of my knowledge. Job Description Are you looking for a patient- oriented, innovation- driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as Manager MS T Analytical Lab (f/m/d) Lead a dynamic team at the forefront of vaccine development, driving innovation and efficiency in biopharmaceutical manufacturing processes, while shaping the future of Takeda s global dengue vaccine operations. Responsibilities: Establish, lead and manage the MS T Analytical Lab Team, overseeing analyses, troubleshooting, and lab activities to support process development and product characterization. Collaborate with DS Labs, DP Labs, international Analytical/ QC departments, and other functions to align analytical strategies, standards and [...] scientific and technical leadership, ensuring high- quality results across biological, molecular, and physical/ chemical methods, while fostering team collaboration and continuous improvement. Serve as the main contact for internal and external partners, managing operational and capital expenditures, safety, training, and documentation. Attract, mentor and evaluate team members, developing talent to meet future competency needs and enhancing analytical capabilities through standardized methods. [...]
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Jobbörse Stellenangebote Manager Product Documentation Jobs gefunden bei Jobbörse Stellenanzeigen.de

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Stellenangebot Manager Product Documentation Job bei PIMCO Prime Real Estate GmbH Job vor 5 Tagen gefunden PIMCO Prime Real Estate GmbH Real Estate Analyst (m/f/d) Acquisition • 60325, Frankfurt am Main, Deutschland Work-Life-Balance
MEHR[...] Acquisitions Sales Team as Analyst (m/f/d) and shape the future of real estate investment for PIMCO Prime Real Estate in the region North Central Europe. Be part of a motivated leading European acquisition sales community and work alongside experienced investment manager together with other European talents. Make the first step into a successful career in the real estate industry at one [...] an active role in the support of due diligence processes for new investments or sales, and the preparation of internal due diligence documents Gain valuable experience by assisting in negotiations related to investments and collaborating on the drafting of transaction documentation. Communicate effectively and professionally with internal and external partners, attending meetings, and build up your own professional real estate network Contribute to regular reporting activities of investments and help to organize global investment forum and other internal conferences Play a part in driving new business and product development across sector strategies, conducting market research and preparing investment strategy papers. Support for any financing activity for standing assets [...]
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Stellenangebot Manager Product Documentation Job bei MC- Bauchemie Müller GmbH Co. KG Job vom 06.11.2024 MC- Bauchemie Müller GmbH Co. KG

Civil Engineer as Product Manager (m/f/d) international Concrete Protection of Water Infrastructure

• 46236, Bottrop, Deutschland Work-Life-Balance
MEHR[...] success story spanning over 60 years, we offer long- term prospects and partnerships to our customers and employees. To expand the technical service team in our headquarters in Bottrop, we are looking for an engaging personality as Civil Engineer as Product Manager (m/f/d) international Concrete Protection of Water Infrastructure Grow with us through diverse responsibilities: After intensive training, you will be responsible [...] concrete repair and surface protection products for wastewater and underground sewer structures. You will initiate and support product innovations from development to application tests, certification, and market launch. As a basis for the sale, you will provide the technical product documentation and work with the technical marketing team on social media posts and website content. Your core tasks include designing and [...]
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Stellenangebot Manager Product Documentation Job bei PAUL HARTMANN AG Neu Job vor 6 Std. gefunden PAUL HARTMANN AG Regulatory Affairs Manager for Clinical Evaluation (f/m/d) • Heidenheim
MEHR[...] commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills and play an active role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements. If you are also enthusiastic about our meaningful product portfolio, we should get to know each other. Responsibilities: Provide and update documentation of clinical evaluation, post- market clinical follow- up and post- marketing surveillance Cross- functional communication with other departments such as [...]
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Stellenangebot Manager Product Documentation Job bei PAUL HARTMANN AG Neu Job vor 6 Std. gefunden PAUL HARTMANN AG

Natural Scientist as Clinical Evaluation Manager (f/m/d)

• Heidenheim
MEHR[...] commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills and play an active role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements. If you are also enthusiastic about our meaningful product portfolio, we should get to know each other. Responsibilities: Provide and update documentation of clinical evaluation, post- market clinical follow- up and post- marketing surveillance Cross- functional communication with other departments such as [...]
Stellenangebot Manager Product Documentation Job bei PAUL HARTMANN AG Neu Job vor 6 Std. gefunden PAUL HARTMANN AG Clinical Research Manager for Regulatory Affairs (f/m/d) • Heidenheim
MEHR[...] commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills and play an active role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements. If you are also enthusiastic about our meaningful product portfolio, we should get to know each other. Responsibilities: Provide and update documentation of clinical evaluation, post- market clinical follow- up and post- marketing surveillance Cross- functional communication with other departments such as [...]
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Stellenangebot Manager Product Documentation Job bei PAUL HARTMANN AG Neu Job vor 6 Std. gefunden PAUL HARTMANN AG

Regulatory Affairs Manager for Post- Market Surveillance (f/m/d)

• Heidenheim
MEHR[...] commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills and play an active role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements. If you are also enthusiastic about our meaningful product portfolio, we should get to know each other. Responsibilities: Provide and update documentation of clinical evaluation, post- market clinical follow- up and post- marketing surveillance Cross- functional communication with other departments such as [...]
Stellenangebot Manager Product Documentation Job bei PAUL HARTMANN AG Neu Job vor 6 Std. gefunden PAUL HARTMANN AG Clinical Evaluation Manager (f/m/d) • Heidenheim
MEHR[...] commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills and play an active role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements. If you are also enthusiastic about our meaningful product portfolio, we should get to know each other. Responsibilities: Provide and update documentation of clinical evaluation, post- market clinical follow- up and post- marketing surveillance Cross- functional communication with other departments such as [...]
Stellenangebot Manager Product Documentation Job bei PAUL HARTMANN AG Neu Job vor 6 Std. gefunden PAUL HARTMANN AG

Life Scientist as Clinical Evaluation Manager (f/m/d)

• Heidenheim
MEHR[...] commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills and play an active role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements. If you are also enthusiastic about our meaningful product portfolio, we should get to know each other. Responsibilities: Provide and update documentation of clinical evaluation, post- market clinical follow- up and post- marketing surveillance Cross- functional communication with other departments such as [...]
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Stellenangebot Manager Product Documentation Job bei PAUL HARTMANN AG Neu Job vor 6 Std. gefunden PAUL HARTMANN AG Regulatory Affairs Manager (f/m/d) • Heidenheim
MEHR[...] commitment you can grow on your job every day. At HARTMANN we believe in the difference you can make. Join our team as DEU- Heidenheim At HARTMANN, you have the opportunity to become part of a global team. As a Manager Regulatory Affairs Clinical (f/m/d) , we offer you a varied and challenging position in an international environment. Here, you can develop your skills and play an active role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements. If you are also enthusiastic about our meaningful product portfolio, we should get to know each other. Responsibilities: Provide and update documentation of clinical evaluation, post- market clinical follow- up and post- marketing surveillance Cross- functional communication with other departments such as [...]
Job vom 02.11.2024 PAUL HARTMANN AG

Manager Global Product Development (f/m/d) - Medical Devices

• Heidenheim
MEHR[...] 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 all relevant rules and guidelines Qualifications: Trained Electrician or Electronics Technician [...]
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