Technical marketing manager állások Németországban (egészségügy, gyógyszeripar)

• Kennenlernen des vollumfänglichen Herstellungsprozesses eines Medikaments – von der Rohstoffverarbeitung bis zur Verpackung
• Arbeiten in einer der modernsten Produktionsanlagen Europas für Arzneimittel
• Begleitung durch erfahrene Teams, die ihr Know-how in der Herstellung fester Arzneiformen weitergeben

Lead and coordinate the Site-Launch activities and associated teams for internal and external sites and development projects...

• Oversee work for timely completion of a complaint investigation and response to the various customers
• Communicate with customers regarding complaints, product issues and returned devices

• Lead and support cross-functional projects in regulatory affairs and quality management.
• Identify, interpret, and implement regulatory requirements across global markets, with a strong focus on international registrations outside the U.S. and EU.

• design hard- and software solutions to address intraoperative workflow problems of surgeons
• gather and integrate customer feedback to refine your designs
• build proof-of-concept demonstrators and test your solutions with product management and clinical partners

• Ensure economic success of ZEISS Microsurgery Visualization Systems by identifying customer needs, defining product strategy, and creating new business models
• Manage the full product lifecycle, balancing customer needs, technical feasibility, and economic constraints to determine what gets built.

• Responsible for the functionality, data quality, compliance, and user-friendliness of RIMS and eCTD systems.
• Ensuring the operation, maintenance and further development of the systems (Extedo eCTDmanager, Veeva RIM).

Collaborating across Kerry's global and cross-functional network to anticipate market trends, understand customer needs, and drive innovative biotechnology solutions that deliver exceptional taste, nutrition, and functionality to the food & beverage industry....

Define and Execute Strategy: Establish and drive the global regulatory strategy for the Pharmaceutical Business Unit, ensuring direct alignment with our commercial objectives and Testo's 2030 vision....

Conduct Interoperability Testing: Perform comprehensive testing of medical imaging devices and software to ensure compatibility and compliance with DICOM standards....

• Derive, structure, and prioritize user stories to guide development based on stakeholder requirements
• Coordinate interdisciplinary and cross-functional teams to implement new features effectively
• Guide and instruct the development team, managing technical dependencies to ensure smooth progress

• Develop strategies for existing and new product portfolios, including market analysis to identify opportunities for innovation
• Analyze market trends and customer needs to inform pricing strategies and target markets

Development of product strategies for existing and new portfolios, including market research to identify innovation opportunities in lens technology and design, as well as defining product specifications and managing the product lifecycle...

• Lead and manage client relationships for pharma and biotech accounts, ensuring satisfaction and longterm partnerships
• Serve as product owner or strategic advisor on key market access projects (AMNOG, EU HTA, pricing, reimbursement)

• Market development in alignment with the Commercial Operations team
• Developing and conducting product trainings (online and classroom)
• Participation in product launch activities
• Answering questions from the local sales and service organizations
• Support on customer visits, exhibitions and congresses

• Lead and inspire a global team of about 30 scientists and technical experts, fostering innovation, collaboration, and excellence.
• Spearhead the formulation and manufacturing process development for small molecule animal health products, from enabling formulations to tech transfer.

• Technical responsibility in development projects in the field of Intraocular Lenses (IOL)
• Responsibility for the technical support of existing products throughout their entire lifecycle and assistance with approval in international markets

Serve as the medical device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, complaints, safety signals, field action, voice of the customer, and voice of the business....