90+ English-Speaking Jobs in Mainz

Designing and operationalizing AI use cases for pharmaceutical product safety. Generative AI, LLMs, and RAG experience required. Hybrid work, flexible hours.

Designing and deploying deep learning pipelines for action quality assessment in MedTech. Experience with DL/CV model deployment and time-based signals required. Monthly shopping vouchers, Urban Sports Club membership.

Global portfolio strategy and investment prioritization for biotechnology drug development. Deep portfolio management expertise required. Flexible hours, vacation account, digital learning.

Governing clinical data integration lifecycle for novel therapies at a global biopharmaceutical company. 10-15 years experience, including 5+ in Clinical Data Integration, required. Bonus and equity options available.

Developing real-time software and hardware solutions for satellite ground systems. Programming in PLC and embedded environments. Hybrid work, 4-day work week.

Developing and maintaining Flutter mobile apps for health and wellness frequency technology. Solid Flutter and Dart experience required. 100% remote work possible, company bike.

Designing and executing immuno-oncology clinical trials from Phase I-III for a biotech firm. M.D. with extensive clinical development and NDA submission experience required. Flexible hours, vacation account, digital learning.

Bioinformatics research for immunotherapy of cancer, infectious diseases, and autoimmunity. Master's degree in a relevant field and English proficiency required. Fully funded position with dedicated supervision and cutting-edge technologies.

Defining business needs for Veeva Network, Vault, and CRM integrations in Life Sciences. Veeva Network, CRM, and Vault experience required. 25 days workflex, CHF 1,500 annual training budget.

Leading proposal activities and studies for future-oriented Earth observation data systems. Business concept development and new project acquisition expected. 4-person team, 3 weeks travel per quarter.

Leading bid/proposal projects for satellite data IT systems and mechatronic solutions. Building customer relationships and identifying market opportunities. Experience in proposal management and solution concept development preferred.

Establishing product quality standards for mRNA-based therapies and identifying risks. Fifteen years of QA experience in FDA/EMA regulated environments required. Flexible hours, vacation account, and leadership development.

End-to-end payroll processing and compliance for Germany, with regional EMEA contributions. German social security and labour law knowledge required. Continuous learning and professional development opportunities.

Conducting research placements with hands-on training in CRISPR/Cas genome editing and NGS. Outstanding Bachelor or Master student enthusiasm required. Stimulating interdisciplinary research environment.

Developing enterprise AI security frameworks and policies for generative AI and MLOps environments. Extensive cybersecurity experience securing AI/ML systems required. Flexible hours, vacation account, digital learning.

Market analysis and mechanical design for satellite ground systems. Support for bidding activities and system engineering tasks. Engaging in calculations and design tasks.

Leading late-stage technical transfer and BLA readiness for novel biologics. Extensive commercial manufacturing and CMC leadership experience required. Flexible hours, vacation account, digital learning.

Supporting global satellite operation and IT solutions projects. Familiarity with satellite data systems preferred. Hybrid work, flexible hours.

Statistical leadership for oncology and infectious disease clinical trials at a biotech firm. 5+ years pharma/CRO experience, including 3 years staff oversight, required. Annual bonus and equity.

Primary contact for after-sales and warranty for satellite data IT systems. Coordinate customer service requests, repairs, and contract extensions. Support throughout warranty period.

Leading a team of structural and mechanical engineers on satellite ground systems projects. Operational involvement and proposal support. Team performance evaluation and corrective action monitoring.

Conducting donor eligibility examinations and medical supervision for plasma donation at a global biopharma subsidiary. Approbation as a doctor required. Family-friendly working hours, no night shifts.

Leading EMEA compliance for a global CGM pioneer, navigating complex multi-jurisdictional healthcare regulations. 8-10 years healthcare compliance experience in medical devices or pharma required. Growth opportunities, in-house learning programs.

Medical safety expertise for oncology drug development, including clinical trial protocol contributions and investigator training. MD/PhD and extensive drug safety experience required. Annual bonus and equity.