analyst English-speaking jobs in Lübeck

Inside Sales Representative (m/f/d) Swedish Market supports existing business customers in the Swedish logistics market. Daily work involves regular contact with assigned accounts, maintaining customer relationships, and identifying additional needs. The role is office-based in Berlin and requires Swedish (native level) and English (professional working level).

Data Analyst (m/w/d) needed for full-time position. Collect, clean, and validate data from various sources. Perform exploratory data analysis, create dashboards and reports, and develop KPIs. Collaborate with business units to understand requirements and provide data-driven solutions.

Leads sales efforts for turf and landscape solutions across key market segments, including landscapers, sports fields, and commercial properties. Develops and executes sales plans, builds client relationships, and provides product expertise.

Develops and maintains scientific relationships with ophthalmology experts. Supports medical affairs and clinical development initiatives, including trial recruitment and medical education. Provides up-to-date medical information and collaborates with internal and external stakeholders.

Working student will devise and implement RF measurement scenarios using off-the-shelf components. Tasks include planning measurements, performing reliable RF measurements (S-parameters, de-embedding), automating data acquisition, analyzing/processing data, and creating reports.

Support vendor onboarding, contract management, and performance reviews. Contribute to project management and optimize workflows. Bachelor's degree in a relevant field with experience in provider management or project management preferred.

ISCC is seeking a Software Engineer – Full Stack to design, develop, and maintain full-stack applications, web services, and REST APIs. Responsibilities include implementing and integrating applications with external systems, automating workflows, and creating technical documentation. The ideal candidate will have a university degree in computer science or a related field, at least 2 years of experience as a full-stack software engineer, and strong proficiency in Go, JavaScript/TypeScript, and Python.

As (Senior) Clinical Trial Supply Manager, you will ensure timely and reliable supply of investigational medicinal products to clinical trials. You will manage end-to-end supply execution, from forecasting and packaging to distribution and returns, collaborating with various departments and vendors.

Intern (m|f|d) - Research & Development - Stock Preparation supports research and development projects in sustainable and efficient paper production. Responsibilities include developing and evaluating test rigs, planning and conducting experiments, and supporting external trials.

Senior Applied Researchers lead improvements, automation, and scaling of data-heavy processes. They tackle projects on image quality scoring, taxonomy improvement, entity resolution, and conflict resolution. Responsibilities include collaborating with management, defining project scopes, seeking scientifically valid solutions, and mentoring junior peers.

Supports Company and Department Leaders with HR processes and issues. Manages employee data, time tracking, absence, learning and development, and assists with hiring. Advises on contractual and labor law issues.

Enterprise Sales Representative will win new manufacturing customers, establish Wandelbots as a strategic platform partner, and lead complex sales cycles from initial engagement to multi-year platform adoption.

Leads installations of technical systems and applications for clients. Provides solutions using Salesforce declarative automation and data integrity tools. Troubleshoots complex client issues and assists in avoiding potential downstream issues. Possesses a thorough knowledge of the nCino data model and functionality. Promotes cross-team collaboration and encourages continuous learning. Requires 8+ years of related experience or equivalent. Salesforce certifications required.

Solution Architect for SAP S/4HANA Source-to-Pay systems. Designs, maintains, and validates technical SAP solutions. Translates functional designs into technical specifications and collaborates with stakeholders to prioritize business demands. Requires 10+ years of IT experience, 8+ years in solution architecture, and 5+ years in global projects. Must have S/4HANA Source-to-Pay certification and experience with SAP ABAP and ALE-IDOC.

Lead the implementation of training strategies across various functions within the Product Line Distribution, Dry, Traction Transformers. Develop and enhance the Product Line Training Management strategy and oversee training, development, onboarding, and certification programs. Drive accountability and increase employee engagement through the implementation of the ITM system.

Design and execute test cases for LLM-based agents, simulating human workflows and defining gold-standard behavior. Analyze agent performance, iterate on test scenarios, and ensure reusability.

Software Developer C++ will design and implement software solutions for medical robotic systems. Responsibilities include defining software requirements, coding, debugging, testing, and ensuring product reliability and safety. Requires a Master's or PhD in a related field and 3-5 years of experience in software design and development, preferably in medical device or robotics industries. Strong proficiency in C++ 17/20 and experience developing real-time applications in a Linux environment are essential.

Supports, expands, and analyzes XL customers, selling DKV Group products. Provides feedback on competitive observations and market trends. Develops the product portfolio in cooperation with specialist departments and other key account managers. Reports and forecasts sales figures. Participates in customer events and sales projects.

Group Regulatory Affairs Specialist will research and determine regulatory requirements and compliance activities for product submissions. Evaluates proposed documents for regulatory filing and provides regulatory input and guidance to product development teams. Manages post-approval activities, including submitting notifiable changes and ensuring compliance with regulations. Requires a Master's degree in science and minimum 3 years experience in Regulatory Affairs for medical devices.

Design and maintain enterprise-level data architectures, ensuring scalability, governance, and interoperability. Lead data modeling workshops, define standards, and create documentation. Establish data quality, lineage, and metadata standards while collaborating with security and compliance teams. Mentor and coach architects and engineers on data literacy and architecture maturity.