5137 visa sponsorship germany English-speaking jobs in Germany

Lead Exterior Designer to develop bold, innovative electric vehicle designs. Experience in automotive exterior design, proficiency in design software, and strong communication skills required.

Do Well Do Good seeks Founding Partners to launch and grow their own consulting offices. Successful candidates will build client pipelines, deliver projects, and achieve €500K revenue in Year 1. Full-time partnership and equity options are offered in Year 2.

Senior Scientist will manage the life cycle of linker-payloads, collaborating with CMOs on development and scale-up. Responsibilities include process design, analytical method development, GMP manufacturing support, and technology transfer. Requires a minimum of 4 years of experience in API process development and scale-up with a PhD or 7 years with a MS degree.

Develop, lead, and implement global regulatory strategies for a pipeline of copper-based theranostic products. Manage regulatory filings (INDs, NDAs) and interactions with global health authorities (FDA, EMA).

Project Manager to lead EV charging infrastructure deployments across central Europe. Manage project budgets, timelines, and technical solutions. Experience in infrastructure, energy, or EV charging project management required.

Senior Interior Designer to lead automotive interior design programs from concept to production. Requires 7+ years of experience in automotive OEM or top-tier design consultancies, a strong portfolio, and proficiency in design tools. Fluent English required.

Founder Associate to support CFO and finance team with day-to-day operations, shareholder and investor relations, and HR processes. Assist with month-end closings, accounts payable/receivable, and procurement.

Shape the future of our mobile platforms as a Product Manager for Mobile Apps. Conceptualize, develop, and lead the roadmap for our native iOS and Android applications, focusing on user experience. Collaborate with designers, engineers, and stakeholders to deliver exceptional mobile experiences.

Senior Scientist Clinical Pharmacology will serve as the clinical pharmacology representative in clinical study and project teams. Responsibilities include ensuring data collection, performing PK/PD analyses, and authoring clinical pharmacology aspects of study documents. Requires a PhD, PharmD, or equivalent with 4+ years of industry experience in clinical pharmacology.

Senior Scientist to develop high-performing production cell lines and robust cell culture processes. Requires expertise in CHO cell lines, transfection, and upstream processing. Must have strong understanding of global CMC regulatory requirements and GxP.

Develops analytical methods for CMC processes, plans and executes experiments, and characterizes ADC assets. Requires experience with mass spectrometry, analytical instruments, and biochemical assays.

Computational Scientist to analyze translational and clinical biomarker data. Apply statistical and computational methods to evaluate biological data and contribute to biomarker strategies and drug development programs. PhD in Life Sciences, Biology, or related field required. Strong experience analyzing biomarker datasets and proficiency in R and Python.

Senior Scientist to provide scientific and operational oversight of biomarker activities in clinical trials. Expertise in immunohistochemistry (IHC) methods and assay development required.

Senior Scientist to oversee outsourced analytical development activities for antibodies, small molecules, and ADCs at CDMOs and CROs. Develop, optimize, and maintain analytical methods and support method transfer. Requires a degree in biotechnology, chemistry, or biochemistry plus 3+ years experience (PhD) or 5+ years experience (Masters). Proven experience in analytical method development and transfer to QC, and supporting outsourced analytical activities.

The Clinical Research Coordinator I conducts and manages clinical trials, ensuring adherence to study protocols, GCP, ICH Guidelines, and Velocity SOPs. Responsibilities include subject recruitment, data collection and management, adverse event reporting, and communication with stakeholders.

The Clinical Research Coordinator I conducts and manages clinical trials, ensuring adherence to study protocols, GCP, ICH Guidelines, and Velocity SOPs. Responsibilities include subject recruitment, data collection and management, adverse event reporting, and communication with stakeholders.

The Director Europe for Onshore Wind and BESS leads commercial strategy and execution for the European market. This role encompasses sales, order intake, customer relationships, and cross-functional delivery coordination. The Director requires deep understanding of the onshore wind value chain and experience leading and closing large-scale turbine supply contracts.

Leads the structural design and engineering of offshore and onshore wind turbine support structures. Manages the design process, ensuring compliance with industry standards and collaborating with multidisciplinary teams.

As a Product Manager for the AI Platform, you will define, scale, and operationalize AI capabilities across Scalable Capital. You will lead the strategy for a unified "AI as a Platform" offering, working with Data Scientists, AI Engineers, and Software Engineers to integrate AI effectively, securely, and ethically. You will drive the implementation of AI use cases, ensuring compliance and governance, and support the launch of client-facing AI features.

The Project Management Office Analyst supports the Portfolio PMO Manager in enhancing portfolio performance by improving the quality and clarity of information used in governance and decision-making. The role focuses on turning complex project data into clear, decision-ready insights, ensuring smooth and predictable portfolio governance.