85+ English-Speaking Jobs in Liesberg

KI-Beschreibung

As a Senior Project Manager for Device Software, you will lead innovative software projects from idea to launch, collaborating with diverse teams to enhance flow meter efficiency and optimize processes in a dynamic, global environment.

• •Several years of experience managing traditional and agile development projects in a software environment
• •Experience with embedded software, software platforms, edge computing, and AI
• •Degree in a technical field or comparable education

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KI-Beschreibung

As a Trainee in Corporate Controlling, you will dive into financial data analysis and reporting while collaborating with various departments. This role focuses on ensuring accurate financial insights and optimizing reporting processes.

• •Proficiency in Microsoft Office (Excel, PowerPoint, Power Automate / Power Query)
• •Strong analytical skills and attention to detail
• •Effective communication skills, both written and verbal

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KI-Beschreibung

As a Trainee in Corporate Controlling, you will engage in financial analysis and reporting, collaborating with various departments to ensure accurate and timely financial insights that drive company success.

• •Proficiency in Microsoft Office (Excel, PowerPoint, Power Automate / Power Query)
• •Strong analytical skills and attention to detail
• •Effective communication skills, both written and verbal

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KI-Beschreibung

In this role as a Clinical Research Associate, you will be actively involved in the clinical monitoring process, ensuring quality and accuracy while coordinating various aspects of clinical trials. Your work will directly contribute to improving health outcomes globally.

• •University degree in a life-sciences field
• •At least 6-18 months independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
• •Oncology disease experience

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KI-Beschreibung

As a Product Owner, you will manage the product backlog and serve as the key link between stakeholders and the development team. This role involves conducting market research, participating in strategic planning, and supporting go-to-market activities to enhance the Netilion ecosystem.

• •Industrial background in Water/Wastewater, Food & Beverage, Life Sciences, or Chemical industry
• •Familiarity with software applications in process automation, asset management, and industrial process management
• •Experience in business development, product management, sales, or strategic partnerships

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KI-Beschreibung

In this role, you will provide medical leadership and oversight for clinical projects, ensuring high-quality scientific input and guiding the Clinical Trial Team. Your day-to-day responsibilities will involve engaging with external experts, conducting safety reviews, and contributing to strategic decisions.

• •At least 5 years of experience in Clinical Development within the pharmaceutical or biotech industry
• •Medical degree (MD)
• •Strong knowledge of drug development and clinical trial process

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KI-Beschreibung

As the Global Market Access Lead for Biologics, you will shape strategies to ensure timely access to innovative therapies, collaborating with teams worldwide to drive successful product launches and develop impactful access solutions.

• •8–10 years of experience in pharma/biotech with a focus on launching innovative biologics and/or biosimilars in global or regional market access role
• •Proven success in developing global access strategies and launch plans
• •Experience with pricing governance, reimbursement submissions, and patient access programs

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KI-Beschreibung

In this role, you will lead a PhD project focused on developing advanced models to understand insecticide resistance. This position involves collaboration with top researchers and sharing findings through publications and presentations.

• •MSc degree or nearing completion in quantitative field or biology/environmental sciences/epidemiology
• •Strong analytical and programming skills
• •Prior experience in Bayesian data analysis or related fields

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KI-Beschreibung

In this role, you will oversee quality assurance for GCP, PV, and GLP activities, ensuring compliance and continuous improvement. Your daily responsibilities will include managing audits, training, and non-conformance issues while supporting inspection readiness.

• •Minimum 10 years of experience in the Pharmaceutical industry
• •Minimum 5 years of experience in QA GCP
• •Excellent knowledge of GCP and PV legislation

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KI-Beschreibung

In this role, you will oversee HEOR projects and collaborate with global teams to develop impactful strategies. Your work will involve mentoring professionals, adapting economic models, and translating data into compelling narratives for stakeholders.

• •8+ years of experience in biotech, pharma, or healthcare sector
• •Strong knowledge of health economic modeling and RWE
• •Advanced degree in health economics, public health, epidemiology, or related field

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KI-Beschreibung

In this role, you will drive patent initiatives in emerging markets while advising leadership on strategies for pharmaceutical development and launches. Your expertise will help shape the strategic direction of the global patent team.

• •5+ years of experience in patent law, ideally within pharmaceutical industry
• •Patent law expertise
• •Qualification as European Patent Attorney (EQE) or equivalent, or attorney-at-law admission

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KI-Beschreibung

As a Clinical Trials Label Program Manager, you will engage with clients to develop tailored label solutions, support the sales team, and ensure smooth project execution. This role involves coordinating studies, training teams, and maintaining key client relationships.

• •Good understanding of clinical trial setup and international regulatory
• •2-3 years of successful project management experience
• •Strong proficiency in digital tools and software

KI-Beschreibung

In this role, you will drive innovation by developing tailored reports and applications, leading a team of programmers, and collaborating with various departments to enhance efficiency. Your expertise will shape the adoption of modern programming practices and ensure the continuous improvement of processes.

• •10+ years within a pharmaceutical company or CRO
• •Master’s degree in Computer Science, Data Science, Machine Learning, Applied Statistics, Mathematics, or related field
• •Extensive R programming experience, including packages like dplyr and ggplot2

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KI-Beschreibung

In this internship program, you will engage in impactful projects while receiving mentorship from experienced leaders. You will have the opportunity to develop innovative solutions in various business areas, shaping your career in the healthcare industry.

• •Demonstrated work experience in healthcare, marketing, sales, finance, project management, strategy, or operations
• •Strong analytical and communication skills
• •Enrollment in MBA, MA, or PhD program

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KI-Beschreibung

In this role, you will lead a dedicated team of project managers, ensuring the successful delivery of clinical supplies projects while enhancing efficiency. Your day-to-day responsibilities will include mentoring the team, addressing client concerns, and driving process improvements to maintain high client satisfaction.

• •5-7 years of experience supporting project management teams
• •Previous work experience in the Healthcare field
• •Accredited degree in a health-related field or advanced degree

KI-Beschreibung

As a Senior Scientific Associate, you will engage in organic synthesis and process development, optimizing reactions and analyzing compounds. This role involves collaboration with the lab team, documentation of experiments, and presentation of research findings, ensuring efficient and safe chemical processes.

• •>5 years of industrial experience in process chemistry or related field
• •MSc or equivalent degree in Chemistry
• •Expert in preparative organic synthesis up to kg-scale

KI-Beschreibung

In this role, you will lead complex clinical pharmacology studies, ensuring timely and quality deliverables. You will collaborate closely with teams, interpret results, and contribute to regulatory documents, all while making a significant impact on the drug development pipeline.

• •At least 10 years’ industrial experience in clinical pharmacology
• •Minimum PharmD degree or preference for PhD/MD
• •Experience in regulatory submission documents and meetings

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