Aktuell 12 English-Speaking Jobs in Freiamt 79348 & Umgebung

KI-Beschreibung

In this internship, you will engage with MPS Automotive products, focusing on validating components and optimizing test processes. Your role will involve hands-on work with lab instruments and collaboration with engineers to enhance product performance.

• •Pursuing a Bachelor or Master Degree in Electrical Engineering, Computer Engineering, Electrical and Computer Engineering, or related field
• •First experience in switched mode power supplies, load switches, linear regulators, motor drivers
• •Hardware bench experience in power electronics and test equipment

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KI-Beschreibung

As a Hardware Testing and EMC Intern, you will engage in hands-on evaluation and validation of components, optimize testing processes, and contribute to exciting projects while collaborating with experienced engineers in a dynamic laboratory environment.

• •First experience in switched mode power supplies, load switches, linear regulators, motor drivers
• •Programming experience (Labview, Python, C, C#)
• •Hardware bench experience in power electronics including PCB design

Deine Vorteile

KI-Beschreibung

As an intern at Monolithic Power Systems in Germany, you will immerse yourself in the dynamic semiconductor industry, contributing to innovative projects while gaining hands-on experience in integrated power semiconductors and systems.

• •Bachelor's degree in Computer Science or related field
• •3 years of experience in software development
• •Proficiency in Java or Python

KI-Beschreibung

In this role, you will be at the forefront of product development and customer support, collaborating with marketing and engineering teams to drive innovative power management solutions for the automotive sector.

• •5-10 years of work experience in Product Definition, System Engineering, or Applications
• •Hands-on experience with PCB board design
• •Experience with lab equipment to test and debug power management ICs

KI-Beschreibung

In this role, you will be at the forefront of drug discovery, tackling ADME challenges and collaborating with multidisciplinary teams. Your expertise will help optimize drug properties and enhance the success of research programs, while also mentoring junior scientists.

• •PhD or equivalent in biology, pharmacology, drug metabolism, pharmacokinetics, or related disciplines
• •Solid knowledge of discovery DMPK, in vitro ADME, pharmacology, and/or biology
• •In-depth knowledge of discovery DMPK, in vitro ADME, and pharmacology-related topics, ideally combined with experience as a DMPK representative in cross-functional research projects

KI-Beschreibung

In this role, you will lead nonclinical drug safety efforts for eye and mental health projects, guiding strategies from discovery through regulatory submission. You will manage multiple development programs and ensure compliance with external standards.

• •DVM, MD or PhD with specialization or strong working experience in toxicology
• •Several years of experience in regulatory nonclinical drug safety for human pharmaceuticals
• •Disease-area knowledge in at least one therapeutic area (Eye health and/or Mental health)

KI-Beschreibung

In this role, you will lead development projects as the CMC subteam lead, driving innovation and ensuring the implementation of high-quality analytical methods. Your responsibilities will include mentoring colleagues and collaborating closely with various teams to enhance drug development.

• •PhD in Chemistry, Biology, or related Life Sciences with experience in the pharmaceutical industry or Master's degree with longstanding experience in the pharmaceutical industry
• •Proficiency in chromatographic techniques such as HPLC-SEC and HPLC-CEX
• •Extensive hands-on experience with electrophoretic methods like CGE, CZE, or icIEF and familiarity with GMP-regulated environments and compliance standards

KI-Beschreibung

In this role, you will drive genomic target and biomarker identification using advanced methodologies and large-scale datasets. Your expertise will shape strategic initiatives and foster collaboration across teams, influencing R&D portfolio advancements.

• •PhD in Statistical Genetics, Bioinformatics, Genetic Epidemiology, Computational Biology, Statistics, Computer Science, or related fields
• •Several years of post-PhD industry experience in disease translation within a pharmaceutical or biotechnology environment
• •Strong statistical genetics expertise demonstrated through successful disease translation applications

KI-Beschreibung

As a Postdoctoral Researcher, you will shape drug discovery by developing and refining human pharmacokinetic prediction methods, collaborating with experts, and sharing findings to drive impactful decision-making in the pharmaceutical industry.

• •PhD in a field related to pharmacometrics
• •Proficiency in R, MATLAB, Phoenix WinNonLin, or NONMEM
• •Proven skills in PK, PK/PD, PBPK, or longitudinal disease modelling

KI-Beschreibung

In this role, you will lead efforts in patient safety by designing risk management strategies and overseeing pharmacovigilance activities. Your expertise will be crucial in evaluating product safety, preparing regulatory documents, and collaborating with teams to enhance patient outcomes.

• •Clinical or research experience in inflammation therapeutics
• •Experience in pharmacovigilance and risk management in a pharmaceutical company
• •Experience in clinical development and submissions for marketing authorization

KI-Beschreibung

In this role, you will play a pivotal part in shaping the enterprise's data management strategy, collaborating with various teams to ensure data is a strategic asset. Your day-to-day responsibilities will involve designing governance solutions, ensuring compliance, and enhancing data quality across the organization.

• •Master's degree in Computer Science or comparable qualification
• •Proven experience driving enterprise-wide data governance and management initiatives
• •Strong knowledge of data management principles, governance tools, and compliance requirements

KI-Beschreibung

In this role, you will empower healthcare teams by providing essential training on device handling and procedures, ensuring they achieve expert proficiency. Your day-to-day responsibilities will include developing training materials, managing case processes, and collaborating with key accounts to enhance patient outcomes.

• •Minimum 3 years of related medical device or clinical experience
• •Bachelor's Degree in related field
• •Knowledge of cardiovascular science

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