Daniel Mazza Email & Phone Number

Nürnberg, Bayern, Deutschland

- Creation and extension of conceptual and logical information models in the pharmaceutical industry.- Development of object-oriented class diagrams in various data domains to describe business logic.- Collaboration with subject matter experts to define and refine models used for technical implementation.- Management of project documentation, progress tracking, and stakeholder communication through Confluence and Jira.- Organisation and moderation of workshops to align conceptual and logical models with business needs.Key Tools & Technologies: UML, Class Diagrams, Data Domain Modeling, Innovator, Jira, ConfluenceIndustry: Pharmaceuticals

Fürth, Bavaria, Germany

- Managed requirements for the certification of medical software as a medical device according to the Medical Device Regulation (MDR).- Handled product and system requirements using IBM Rational DOORS in an interdisciplinary Scrum environment.- Developed use case documentation and designed business processes using Enterprise Architect.- Contributed to the regulatory compliance of software by researching and defining requirements based on ISO standards.- Created a functional concept for document management as part of my Master's thesis.Key Tools & Technologies: IBM Rational DOORS, Enterprise Architect, SQL, Scrum, BPMNIndustry: Medical Software

Fürth, Bavaria, Germany

- Supported the software validation processes at Siemens Mobility using the data analytics tool KNIME.- Developed and maintained workflows for automated software validation reports.- Configured user interfaces and connected various data sources to streamline analytics processes.- Managed versioning and error tracking through TortoiseSVN and Redmine.Key Tools & Technologies: KNIME, Python, TortoiseSVN, RedmineIndustry: Mobility

Fürth, Bavaria, Germany

- Work in a multidisciplinary team (13 specialties) from 11 different nationalities- Working with agile methods- Creating a clinical evaluation report for a medical product using SQL database queries, data preparation, and data analytics- Design and customization of information systems- Design and implementation of a document management system to support agile software development- Support of activities to ensure regulatory compliance of a software as a medical device- Creation of process documents and templates- Research on and definition of regulatory requirements such as Regulation (EU) 2017/745 on Medical Device Regulation; ISO 13485 (Medical devices - Quality management systems - Requirements for regulatory purposes) and IEC 62304 (Medical device software - Software lifecycle processes)

Nuremberg, Bavaria, Germany

- Support with business consulting projects- Support with the annual audit- Preparation of presentations- Various research activities- Data preparationProject report: New ways of business consulting for inpatient care facilities in GermanyDerivation of a modular consulting concept for care rate negotiations

Master Of Arts - Ma, Business Administration And Management, General, 1.5

Bachelor Of Arts - Ba, Health/Health Care Administration/Management, 1.6