Aktuell 109 English-Speaking Jobs in Ginsheim Gustavsburg & Umgebung

KI-Beschreibung

In this temporary role, you will play a key part in supporting pricing and commercial conditions, conducting analyses, and creating essential reports. Your day-to-day responsibilities will involve collaborating with the team to ensure data quality and assist in market reviews.

• •Advanced MS Office skills and basic SAP skills
• •Financial understanding and good analytical skills
• •Ability to provide insights with confidence

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KI-Beschreibung

In this role, you will play a crucial part in transforming the architecture by collaborating with various teams and stakeholders. Your focus will be on simplifying IT landscapes and addressing the evolving needs of the financial services sector.

• •Extensive experience in IT Architecture on enterprise level
• •Proven ability to simplify, modernize, and digitize IT landscapes
• •Comprehensive knowledge of modern IT technologies

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KI-Beschreibung

In this role, you will play a crucial part in transforming the enterprise architecture by collaborating with various teams and stakeholders. Your focus will be on simplifying complex IT landscapes while addressing the evolving needs of the financial services sector.

• •Extensive experience in IT Architecture on enterprise level
• •Proven ability to simplify, modernize, and digitize IT landscapes
• •Comprehensive knowledge of modern IT technologies

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KI-Beschreibung

In this role, you will lead product development within a Quality Management System, ensuring compliance with key regulations while driving innovation. Your day-to-day responsibilities will involve guiding teams, managing product changes, and fostering a culture of excellence.

• •Extensive experience in pharmaceutical product development, Quality Assurance, and GMP compliance
• •Proven track record of leading product lifecycle management and strategic initiatives
• •Deep understanding of ICH guidelines (Q8, Q9, Q10) and their application

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KI-Beschreibung

In this role, you will lead the global manufacturing network's quality assurance efforts, driving compliance and strategic changes while fostering a collaborative team culture. Your day-to-day responsibilities will involve guiding critical decision-making and ensuring operational excellence across multiple regions.

• •Extensive experience in Quality Assurance, GxP compliance, and manufacturing operations within the pharmaceutical industry
• •Significant experience in steering external manufacturing networks
• •Demonstrated success in preparing and executing commercial product launches from a Quality Assurance perspective

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KI-Beschreibung

In this role, you will drive efficiency by designing and maintaining a comprehensive process architecture, collaborating with teams to enhance processes through automation and AI, and ensuring compliance with management guidelines.

• •Degree in industrial engineering, business administration, IT, or comparable qualification
• •Several years of professional experience in process management, process architecture, or similar role
• •Proficiency in process modeling and architecture frameworks, such as BPMN 2.0 and APQC, and experience with process management tools

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KI-Beschreibung

In this role, you will lead a team to enhance statistical programming efficiency, ensuring high-quality data analysis and compliance with regulatory standards while collaborating with various departments to meet project timelines.

• •15+ years experience in pharmaceutical industry, CRO, or clinical research setting with focus on oncology
• •Excellent knowledge of statistical programming in SAS including Base, macro, STAT, GRAPH, SQL
• •Bachelor’s degree in Statistics, Mathematics, Computer Science, or related discipline

KI-Beschreibung

As a Medical Director in Clinical Development, you will define and execute strategies for innovative Infectious Diseases programs, lead cross-functional teams, and drive clinical trial design to enhance patient outcomes in a fast-paced environment.

• •MD or MD-PhD with clinical background in infectious diseases
• •Multiple years of experience in vaccine or therapeutic development
• •Expertise in clinical trial strategy, design, and execution

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KI-Beschreibung

In this role, you will immerse yourself in a dynamic research environment, gaining hands-on experience in cutting-edge techniques while collaborating with top scientists and enhancing professional skills.

• •Bachelor or Master student

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KI-Beschreibung

As a Data Quality Expert, you will play a crucial role in promoting Ataccama ONE across business units, educating stakeholders on data quality initiatives, and translating technical requirements into actionable insights that drive business benefits.

• •Hands-on experience with Ataccama ONE
• •Strong technical understanding of data architecture
• •Experience implementing KPI monitoring and data quality rules

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KI-Beschreibung

As a Clinical Safety Manager, you will play a crucial role in overseeing safety and pharmacovigilance during clinical trials, ensuring compliance with regulations while safeguarding patient safety and enhancing global health.

• •Minimum 3 years of clinical research and pharmacovigilance experience
• •Strong knowledge of GCP, GVP, and regulatory requirements
• •Advanced degree in life sciences, pharmacy, public health, or related field

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KI-Beschreibung

In this role, you will engage with donors by conducting eligibility exams and providing essential information about plasma donation, all while ensuring their safety during the donation process.

• •Approbation als Arzt/Ärztin
• •Verantwortungs- und Einsatzbereitschaft
• •Teamarbeit

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KI-Beschreibung

In this role, you will take charge of specific sub-processes within the Source-to-Pay framework, collaborating with global stakeholders to enhance efficiency and drive digital transformation while ensuring compliance and alignment with organizational goals.

• •10+ years of experience in procurement or related field within large-scale, multinational environment
• •Bachelor's or Master's Degree in Business, Finance, Supply Chain, or related field
• •Proven ability to lead and influence in a matrixed, global environment

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KI-Beschreibung

In this strategic leadership role, you will be the technical voice for RNA and antibody products, ensuring compliance and driving excellence throughout the product lifecycle, from development to post-launch support.

• •Advanced degree in Biotechnology, Biochemistry, Chemical Engineering, or related field
• •Extensive experience in late-stage product development, commercial manufacturing, and technical lifecycle management
• •Proven track record in CMC leadership, including technical transfer, regulatory submissions, and post-approval change management

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KI-Beschreibung

In this role, you will play a key part in enhancing DD&I's processes by assisting with internal initiatives, identifying efficiency improvements, and conducting data analysis. Your contributions will help shape training materials and develop tools for effective business intelligence communication.

• •Currently pursuing a degree in Business Administration, Computer Science, Industrial Engineering, or a related field
• •Strong analytical skills
• •Proficiency in Microsoft Office applications, particularly Excel and PowerPoint

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KI-Beschreibung

In this role, you will support researchers in adhering to data management guidelines while ensuring data quality and compliance. Your daily responsibilities will include managing the research data sharing platform and educating staff on best practices.

• •Master’s degree or equivalent qualification in bioinformatics, computational biology, biological science, computer science, or other fields
• •Experience in working with big data, data management, and data repositories
• •Excellent written and oral communication skills in English

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KI-Beschreibung

In this role, you will focus on improving patient outcomes while driving the success of the Specialty Business Unit. Daily activities will involve strategic sales conversations, project management, and collaboration with healthcare professionals to enhance care in the region.

• •Experience in supporting specialists
• •Experience in clinical work
• •Experience in organizing training events

KI-Beschreibung

In this role, you will be at the forefront of safety data analysis, transforming complex datasets into actionable insights while enhancing the analytics platform. Your work will directly support regulatory submissions and improve safety assessments across the innovative product portfolio.

• •Master’s degree in life sciences, computational sciences, data sciences, or related fields
• •Multiple years of experience in pharmaceutical/biotech data analysis and the pharmaceutical industry
• •Strong knowledge of pharmacovigilance regulations (GCP, GVP) and FDA, EMA, and ICH guidelines

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KI-Beschreibung

As a Senior Data Engineer, you will take charge of the entire data lifecycle, from ingestion to transformation, creating data products that enhance AI capabilities and drive intelligent decision-making in hearing care.

• •5+ years of hands-on experience with complex ETL processes
• •Production experience with modern cloud data warehouses (Snowflake, BigQuery, Redshift) on AWS, GCP, or Azure
• •Proficiency in building and optimizing data transformations and pipelines in Python

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KI-Beschreibung

In this role, you will be at the forefront of scientific writing, generating essential documents for novel therapies from discovery to marketing approval. Your expertise will guide teams, ensure compliance, and foster knowledge in writing practices and regulatory standards.

• •>10 years hands-on experience in drug development in therapeutically relevant field, preferably oncology and/or immunology
• •>10 years hands-on experience as scientific or medical writer in pharmaceutical/biotech industry
• •Relevant life science university degree, ideally M.D., Pharm. D, or Ph.D.

KI-Beschreibung

In this role, you will lead the development and execution of biomarker strategies for oncology programs, ensuring alignment with clinical objectives while collaborating with cross-functional teams to drive R&D success.

• •Ph.D. or MD in Immunology, molecular biology, pathology, or related discipline
• •6 to 10+ years of oncology clinical development experience
• •Experience with innovative assay development and problem-solving

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KI-Beschreibung

In this role, you will navigate the complexities of regulatory affairs for diagnostic and medical device products, ensuring compliance while driving market access. Your expertise will be crucial in managing submissions and adapting to evolving regulations.

• •Relevant higher education (Master's degree or PhD) or extensive professional experience (typically >5 years)
• •Proven experience in regulated, quality-controlled environments
• •Skilled in preparing and assembling regulatory documents

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KI-Beschreibung

In this role, you will lead global regulatory efforts for development projects, shaping strategies for interactions with health authorities and overseeing the preparation of essential regulatory documents. Your expertise will help navigate the evolving regulatory landscape and ensure successful product authorization.

• •University degree in natural sciences or equivalent
• •9+ years of working experience in Regulatory Affairs
• •Experience in development of antibody- and ADC-based cancer therapies

KI-Beschreibung

In this role, you will drive complex projects and strategic initiatives, enhancing operational efficiency across drug development. Your day-to-day responsibilities will involve collaborating with senior leadership and fostering innovation within diverse teams.

• •Advanced degree (PhD, PharmD, MD, or MSc) in Life Sciences, Medicine, Pharmacy, or related field
• •Over 5 years of proven experience leading cross-functional teams
• •Expert knowledge of pharmaceutical drug-development processes

KI-Beschreibung

As a Technical Product Manager Lead, you will modernize the data landscape by guiding product strategy and collaborating with teams to ensure solutions are effective and aligned with business needs. This role involves translating insights into actionable decisions and driving best practices.

• •Significant experience as a product owner, technical product manager, or similar role in a data-centric environment
• •Proven track record of launching and scaling technology products and services in an enterprise environment
• •Strong understanding of the modern data stack, including data platforms such as GCP BigQuery, Snowflake, or Databricks

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KI-Beschreibung

In this role, you will focus on enhancing quality processes through digitalization, collaborating with various teams to optimize workflows and ensure compliance with data integrity standards. Your work will drive continuous improvement and automation across the organization.

• •Bachelor's degree in Engineering Informatics, Technology, or similar
• •3-5 years of practical experience in quality engineering within a GMP environment
• •Knowledge of SAP-QM and preferably in Signavio

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KI-Beschreibung

In this role, you will lead the creation of high-quality scientific documents while managing a dynamic team. Your day-to-day responsibilities will include writing, coordinating, and ensuring compliance with regulatory standards, all while fostering a collaborative environment that adds value to the organization.

• •>10 years hands-on experience in drug development in a therapeutically relevant field, preferably in oncology and/or immunology
• •>10 years hands-on experience as a scientific or medical writer in the pharmaceutical/biotech industry
• •Relevant life science university degree, ideally M.D., Pharm. D, or Ph.D.

KI-Beschreibung

In this role, you will lead compliance efforts across Global Technical Development, ensuring training alignment and audit readiness while developing frameworks that support GxP requirements. Your expertise will help maintain data integrity and drive continuous improvement initiatives.

• •Master’s degree in pharmacy, Chemistry, Life Sciences, or related field
• •5+ years in pharmaceutical development, process improvement, or compliance
• •Deep understanding of global GxP requirements and regulatory frameworks

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KI-Beschreibung

In this role, you will play a crucial part in product development and regulatory submissions for RNA and protein-based therapeutics. You will ensure that analytical methods meet GMP standards while collaborating with cross-functional teams and external partners.

• •Advanced university degree in a scientific discipline
• •Industry experience in CMC development/commercial
• •In-depth knowledge of analytical techniques with hands-on experience in assay development and validation

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KI-Beschreibung

As a Driver/Data Collector, you will be on the move capturing high-quality visuals of streets and key locations. This role involves using advanced equipment to gather data that enhances a leading online mapping platform, ensuring every detail is documented.

• •At least 5 years of driving experience
• •Valid EU-issued driver’s license
• •Professional driving experience (e.g., taxi, delivery, logistics)

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