06.06.24 | Teilzeit, Vollzeit | Berlin | E.ON Digital Technology GmbHThe organization who are accountable for delivering E.ON's ambitious digital transformation programs, to empower us on our way towards a digital-first energy company. - Account Development Work closely with our teams to understand client needs and challenges, helping to establish and guide strategic account
Später ansehen06.06.24 | Vollzeit | München | EGYM GmbHStrategy - Guidelines You maintain writing and design guidelines for instructional content - Translation & Project Management You are responsible for day-to-day translation project management, including communication with vendors and reviewers, final QA, as well as release, publication, and deployment
Später ansehen07.06.24 | Vollzeit | München | Infineon Technologies AGguidelines - Drive foundry assessment and selection process within RFQ (incl. Risk assessment) - Drive negotiation aspects for business award in line with business needs - Interface to Contract Management to guide them with business needs This position is suitable for full- and part-time. Your Profile You
Später ansehen03.06.24 | Teilzeit, Vollzeit | Unterföhring | Allianz Global Corporate & Specialty SEAdvice on cross-border insurance of risks abroad and support the regular updating of our International Licensing Guide. - Develop strategic positions on legal topics jointly with our colleagues of various Allianz Commercial locations worldwide. - Participate in the conception, planning and performance
Später ansehen03.06.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHAnd resolution of contract management issues, oversight of timely and accurate site payments, and oversight of the CRO deliverables to ensure complaint and timely execution of site contracts. The position is responsible for adherence to all processes and guidelines along with the CRO relationship management
Später ansehen01.06.24 | Vollzeit | Berlin | ZEISSResearch project management in the medical device/ pharma industry or with contract research organizations - In-depth knowledge of relevant regulatory requirements for clinical studies and clinical evaluations for medical devices (ICH-GCP, ISO 14155, MDR, MPDG, MDCG, MEDDEV, IMDRF guidelines
Später ansehen06.06.24 | Vollzeit | München | Publicis SapientAnd the team's experience and expertise, to guide product development; then validate that learning with user testing - Translate product strategy into a roadmap containing well-defined and prioritized user stories, and features and enablers that will realize the product vision to assist the client in achieving
Später ansehen31.05.24 | Vollzeit | Berlin | ZEISSIn-depth knowledge of relevant regulatory requirements in clinical evaluations for medical devices (MDR, MPDG, MDCG, MEDDEV, IMDRF guidelines) Other knowledge - Good knowledge in biostatistics, data interpretation, and critical reading of publications - Good knowledge of regulatory requirements for CE, FDA
Später ansehen31.05.24 | Vollzeit | Berlin | ZEISSKnowledge of relevant regulatory requirements in clinical evaluations for medical devices (MDR, MPDG, MDCG, MEDDEV, IMDRF guidelines) Other knowledge - Knowledge in biostatistics, data interpretation, and critical reading of publications - Knowledge of regulatory requirements for CE, FDA, NMPA, Health
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