Aktuell 114 English-Speaking Jobs in Mainz 83052 & Umgebung

KI-Beschreibung

In this role, you will oversee TMF compliance and quality across clinical trials, ensuring readiness for inspections and effective documentation practices. You will collaborate with various teams, manage vendor relationships, and drive continuous improvement in TMF operations.

• •University degree or comparable professional education in medicine, life sciences, paramedical sciences, information management, or business administration
• •Minimum of 8 years in the pharmaceutical industry or clinical development roles
• •At least 5 years of TMF-focused responsibilities

KI-Beschreibung

In this role, you will play a vital part in advancing medical safety and pharmacovigilance by tracking important safety information, preparing legal templates, and filing essential documents while supporting the team's ongoing needs.

• •Valid student status and studying medicine, pharmacy, or life sciences
• •Basic knowledge of drug safety and pharmacovigilance principles
• •Experience in clinical trials

KI-Beschreibung

In this role, you will drive strategic growth by developing account strategies for key tech customers while integrating product development into sales workflows. You will build strong partnerships with senior decision-makers and ensure compliance with legal frameworks, all while staying ahead of industry trends.

• •Master’s degree in Industrial Engineering, Optics, Physics, or related technical field
• •Several years of experience in international key account management
• •Solid knowledge of consumer electronics, optics, and AR technologies

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KI-Beschreibung

In this role, you will lead the design and optimization of contract life cycle management processes, ensuring compliance and efficiency. You will collaborate with cross-functional teams to drive improvements and establish governance frameworks, while monitoring performance metrics to enhance the overall process.

• •5+ years of experience in contract management, Legal, Finance or Procurement; previous experience in a similar role highly preferred
• •Strong understanding of financial regulations and contract law
• •Proven experience with contract management software and tools

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KI-Beschreibung

In this role, you will be at the forefront of liquid biopsy advancements, evaluating ctDNA methodologies, leading data analysis, and collaborating with teams to ensure the success of clinical trials and research programs.

• •Ph.D. in Molecular Biology, Oncology, Genetics, or related field
• •Proven experience in ctDNA data analysis and results interpretation
• •Demonstrated ability to independently plan and execute projects

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KI-Beschreibung

In this role, you will lead the development of protein-based products, ensuring compliance with regulatory standards while fostering a collaborative team environment. Your daily responsibilities will include overseeing product changes, managing deviations, and driving excellence in quality assurance.

• •Degree in Life Sciences, Pharmacy, Chemistry, Engineering, or related field
• •Extensive experience in R&D Quality or Product Quality
• •Deep understanding of ICH guidelines (Q8, Q9, Q10)

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KI-Beschreibung

In this role, you will lead the design and implementation of compliance processes for third-party due diligence, ensuring effective risk management while collaborating with various divisions. Your expertise will be crucial in navigating complex transactions and fostering seamless compliance integration.

• •Bachelor’s degree in Law or Compliance degree
• •5+ years of experience
• •Proven expertise in compliance management

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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 shape the global commercial strategy for lung cancer therapies, drive new product planning, and collaborate with cross-functional teams to ensure successful market positioning and launch readiness.

• •8–12+ years of relevant experience in oncology commercial strategy, new product planning, launch readiness, or asset strategy roles
• •Significant experience in early-stage commercialization, including product concept shaping, indication assessment, and early launch strategy
• •Strong track record in solid tumors, ideally with direct or adjacent lung, head and neck cancer experience

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 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 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

Deine Vorteile

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

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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