27 English-speaking jobs in Mainz

  • KPMG
  • Mainz
  • August 11
Assistant Manager in Global Quality & Risk Management develops policies and guidance for the Advisory Business. Requires 3+ years in Risk Management/Compliance, knowledge of GQ&RM processes, and strong communication skills.
  • Novo Nordisk Pharma
  • Mainz
  • August 11
Own and coordinate end-to-end German payroll as the subject matter expert. Manage processing, reporting, and benefits while driving continuous improvement and ensuring compliance.
  • Fusion Consulting
  • Mainz
  • August 11
Senior Data Strategy & Migration Consultant for Pharma. Lead data strategy, architecture, and governance, managing end-to-end migration in regulated environments. Requires 8+ years in data strategy with pharma domain knowledge.
  • Fusion Consulting
  • Mainz
  • August 11
Proactive Data Quality Expert needed to support Ataccama ONE adoption in a pharmaceutical setting. This role involves implementing data quality KPIs, educating stakeholders, and translating business needs into technical configurations.
  • Fusion Consulting
  • Mainz
  • August 11
Senior SAP PLM Consultant to support S/4HANA transformation. Focus on PLM process design and implementation during template build, integrating with SAP ERP and master data architecture. Requires 5+ years of PLM consulting experience.
  • Fusion Consulting
  • Mainz
  • August 11
Senior Functional Consultant needed for Veeva Network implementation in Animal Health Pharma. Lead design, configuration, and deployment of CMDM solutions, requiring expertise in customer, master, and commercial data.
  • BioNTech
  • Mainz
  • August 11
The Director Safety Physician provides medical safety expertise to oncology therapeutic areas, ensuring patient safety throughout clinical trials. Responsibilities include safety data assessment, signal detection, and compliance with GCP and regulatory reporting.
  • BioNTech
  • Mainz
  • August 11
Director Program & Production Procurement CDMO / CMO drives procurement strategies for CDMO/CMO services, focusing on protein-based modalities. This role requires 5-10 years in procurement/program management with CDMO/CMO experience and 5+ years of leadership.
  • BioNTech
  • Mainz
  • August 11
Senior Director Global Quality Supply provides global oversight of QA, compliance, and integrity for clinical and commercial supply. This role ensures GMP and GDP compliance across packaging, labeling, serialization, storage, and distribution.
  • BioNTech
  • Mainz
  • August 11
Associate Director, Senior Data Analyst in Clinical Sciences. This role acts as a technical SME in Clinical Data and Analytics, supporting clinical solutions, managing vendor interactions, and ensuring GxP compliance. Requires 10-12+ years in Clinical Operations/Data Management.
  • BioNTech
  • Mainz
  • August 11
Lead deployment and optimization of ICSM SAP module within CTSM. Act as Business Process Owner for the CTSM digital ecosystem, ensuring seamless data flow and process alignment across clinical trials.
  • BioNTech
  • Mainz
  • August 11
Director MS&T leads technical lifecycle management for RNA and antibody commercial products. This role ensures regulatory compliance, drives technical excellence from PPQ through launch, and manages CMC interfaces and strategic partnerships.
  • BioNTech
  • Mainz
  • August 11
Director AS&T Projects & Strategy coordinates analytical activities for late-stage ADC protein pipeline development. This role represents analytics in interdisciplinary CMC teams and owns the analytical CMC Module 3 package.
  • BioNTech
  • Mainz
  • August 11
Lead global speak-up and investigation processes to safeguard integrity. Manage internal investigations, legal assessments, and disciplinary recommendations. Requires a legal degree and 10+ years of experience.
  • BioNTech
  • Mainz
  • August 11
Systems Engineer SAP BTP Administration ensures seamless operation and governance of SAP BTP services. Responsibilities include managing identity via IAS/IPS, supporting S/4HANA in ECS, and overseeing BTP services like Integration Suite.
  • BioNTech
  • Mainz
  • August 11
Associate Director Scientific/Medical Writing ensures high-quality scientific and regulatory document creation for therapeutic agents. Responsibilities include writing, editing, and managing outsourced medical writing tasks. Requires relevant science/medical degree and 5+ years in drug development.
  • Ubisoft
  • Mainz
  • August 11
Lead 3D Programmer for Beyond Good and Evil 2. Lead and mentor 3D programmers, owning technical direction for rendering and real-time 3D features. Requires 5+ years in game development with strong C/C++ and 3D API knowledge.
  • BioNTech
  • Mainz
  • August 11
Senior Director, Safety Sciences Lead guides safety teams, develops strategies for new marketing authorizations, and oversees surveillance, signal detection, and risk management across global departments.
  • Novo Nordisk
  • Mainz
  • August 4
LogoOwn and coordinate end-to-end German payroll as a subject matter expert. Manage processing, reporting, and benefits while driving continuous improvement and ensuring compliance.
  • Plansee SE
  • mainz
  • July 31
Lead the global engineering network for Plansee HPM, driving digital transformation and standardizing CAD, CAM, and PLM tools. Manage international teams and champion automation within the engineering organization.
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