Quality & Compliance Manager, IT Auditor, Computer System Valididation verfügbar

Quality & Compliance Manager, IT Auditor, Computer System Valididation

verfügbar
Profilbild von Anonymes Profil, Quality & Compliance Manager, IT Auditor, Computer System Valididation
  • 4051 Basel Freelancer in
  • Abschluss: nicht angegeben
  • Stunden-/Tagessatz: 140 €/Std. 1100 €/Tag
    Verhandelbar, Remote Raten möglich
  • Sprachkenntnisse: deutsch (Muttersprache) | englisch (verhandlungssicher)
  • Letztes Update: 16.07.2019
SCHLAGWORTE
DATEIANLAGEN
CV and Project List

Diese Anzeige ist nur für angemeldete Nutzer möglich.

SKILLS
Digital Health Tech Compliance & Quality Management, IT Audit& IT Security Management, Business Analysis/ Requirements Engineering Specialist for Software Development of Medical Device Software and Computerized Systems with Coaching Change and Communication Management background and strong experience in global IT and Business Transformation Programs.
  • More than 18 years’ experience in global corporate positions and multi-cultural and multi-disciplinary projects and programs with extensive know-how and working experience in the regulated Life Science and Health Sector
  • Experience in managing near-shore and / or off-shore teams across multiple locations
  • Excellent writer, presenter, moderator and facilitator for global projects with large audience
  • Customer focused, motivation to exceed expectations and go the extra mile
  • Consulting Services:
    • Regulatory Compliance and Audits within Pharmaceuticals and Medical Device industry (EMA, FDA, PIC/S, ISO, MDD)
    • Quality Management and Assurance for Software Development of Medical Device Software and Computerized Systems (13485,
    • Quality Risk Management (FMEA, ISO 14971)
    • Software Validation and Verification (IEC 623304/82304, GAMP 5/ CSV)
    • Information Security Management ISO 27001 (TÜV SÜD Training as Compliance Officer TÜV SÜD, Certification in 09.2019, Lead Auditor Certification planned for 02.2020)
    • Business Analysis/ Requirements and Usability Engineering (BABOK, IREB, IEC 62366)
    • Business Process Modeling & Transformation, BPMN 2.0
    • Digital and Mobile Solutions Development, Digital Health, Agile/Scrum, Design Thinking
    • Change and Communication Management, Systemic Organizational Development
    • Systemic Business Coaching (St. Galler Management Modell)

Competencies
Languages
  • English – business fluent
  • German – native
Business Software, Hardware, Firmware
  • ITSM IT Service Management – BMC Remedy ITSM Suite, SAP NetWeaver, SAP Solution Manager, Service Now
  • Service Now Discovery for IT Infrastructure
  • JIRA Service Desk for IT Demand Management and Software Development
  • CONFLUENCE Content Collaboration-Software
  • ERP – SAP SCM, MM-PUR, WM, PP, PM Plant Maintenance, MMP Procurement (Material Management) incl. all objects: BOM, PR, SL, Contract and Purchase Order, Order Fulfillment (Sales Order Management), Vendor Master Data (including SIM Tool authorization), Quality Master Data, R/3 HR, ESS
  • SAP Hana Cloud (Application for Digital Home & Healthcare)
  • MES Manufacturing Execution Systems (ATLAS, PAS-X, PMX), MMC Material Movement Controller
  • Test Management - HP Quality Center/ PROTON Test Software, SAP Solution Manager (Implementation, Test Workbench)
  • BPM Business Process Modelling – ARIS
  • CMS Content Management – Vignette, Microsoft Office SharePoint Server (ECM), MODx, TYPO3, Wordpress, HTML
  • Document Management - Documentum D2 and Life Science Suite, Veeva, Microsoft SharePoint
  • CRM Customer Relationship Management – Mamis (Deloitte), vtiger, Daylite, salesforce
  • Project Management - Microsoft Project, Biquanda (ehem. OpenTime), Open Workbench, Sciforma, Project Scheduler, GRANEDA Dynamic, GANTT project, MindManager
Education and Training
  • M.Sc. INFORMATION TECHNOLOGIES IN HEALTHCARE, Donau Universität Krems, 09/2019 – 07/2021
  • B.Sc. CLINICAL AND HEALTH PSYCHOLOGY, SRH Riedlingen, 12/2018 – 12/2022
  • ISO 27001 Compliance Officer & Lead Auditor, Certificate TÜV Rheinland, 06/2019 – 02/2020
  • IT AND CYBER SECURITY & DATA PROTECTION FOR MEDICAL DEVICES, Certificate Johner Institute, Konstanz (05/2018)
  • REGULATORY AFFAIRS FOR MEDICAL DEVICES, Certificate Johner Institute, Konstanz (05/2018)
  • IREB Certificate, CPRE Certified Professional for Requirement Engineering (10/2018)
  • HUMAN FACTORS/ USABILITY ENGINEERING (IEC 62366, IEC 60601, ISO 14971, FDA), Certificate Johner Institute, Konstanz (09/2018)
  • MEDICAL DEVICE SOFTWARE DEVELOPMENT, VALIDATION AND VERIFICATION, Certificate Johner Institute, Konstanz (06/2018)
  • REQUIREMENTS ENGINEERING FÜR BUSINESS ANALYSTEN, Certificate, SGO Zürich (10/2017 – 04/2018)
  • BPMN 2.0 BUSINESS PROCESS MODEL AND NOTATION, Certificate, SGO Zürich (10/2017 – 04/2018)
  • GROUP DYNAMICS, Certificate, SGO Zürich (10/2017 – 04/2018)
  • eREGULATORY AND INTELLIGENCE/ ISO IDMP, Drug Information Association DIA, Philadelphia/US (06/2015)
  • SYSTEMIC BUSINESS COACHING/ St. Galler Management Model, University of Applied Sciences: Technology, Business and Design, Wismar (02/2014)
  • CERT. PROJECT QUALITY MANAGER, IT-Project Management & Computer System Validation in pharmaceutical industries, Novartis (11/2013)
  • SAP DATA MIGRATION MANAGER (Novartis Project Role to implement API Business) (2013)
  • SUPPLY DATA MANAGER SAP SCM/ Supply Chain Data Management in pharmaceutical industries, Novartis (02/2013)
  • OPERATIONAL SOURCING MANAGER SAP SCM/ Contract & Price Management in pharmaceutical industries, Novartis (06/2014)
  • CERT. SYSTEMIC CONSULTANT/ AGENT FOR CHANGE MANAGEMENT & ORGANIZATIONAL DEVELOPMENT Alwart institute, Hamburg (02/2013)
  • JOURNALIST FOR PUBLIC RELATIONS & PRESS OFFICE MANAGEMENT, German Institute for Publicity & Journalism, Hagen (09/2008)
  • MANAGEMENT ASSISTANT BUSINESS ADMINISTRATION Apprenticeship, Volkswagen/Audi, Dortmund (06/2002)
  • DIPLOMA IN BUSINESS ADMINISTRATION, Commercial College, Unna (06/1999)
PROJEKTHISTORIE
Self-employed since 2006:
CEO, Quality & Compliance Manager, Auditor
Digital Chameleon GmbH, Basel/CH

07/2019– today
Project Manager, Development Software as a Medical Device (SaMD)
Service Delivery and direct report to Program Lead
Sanofi Aventis, Frankfurt/DE and worldwide
  • Project Management within Global Program for Software Development of several Apps as Software as a Medical Device (SaMD)
  • Giving Strategy and Advice to establish and improve Corporate Framework within existing QMS 13485 for Software Development, Verification and Validation of Health Apps
  • Quality Management support to extend QMS 13485 with relevant procedures and working instructions for 
  • Regulatory Compliance with new Medical Device Regulation (MDR) in regard to SaMD, transfer to class 2a nd 2b
  • Business Process Design within SharePoint and other Tools for usage as a regulated and validated QMs, Lifecyle and Document Management System (Workflows, Templates, Technical File, Electronic Records and Signatures)
06/2019– 08/2019
Quality and Compliance/ CSV Strategy Consultant, Medical Devices ISO 13485/ MDR
Service Delivery and direct report to Head of Quality Management
Camlog/Altatec GmbH, Basel/CH, Wimsheim/DE
  • Conduct Audit and Inspection Readiness for MDR, MSDAP and ISO in the area of Computer System Validation
  • Giving Strategy and Advice to establish and improve a Corporate Framework within existing QMS 13485 for Computer System Validation, implementing a corporate procedure for CSV including templates for validation management
  • Implementing CSV Strategy into ITIL processes within IT Department
  • Concepting of Validation Strategy for the Re-validation of current IT Systems as part of the QMS, fulfilling requirements from FDA (820.20, Part 11), Annex 11 and ISO 13485, execution of all validation activities and documentation
  • Develop Validation Lifecycle Documentation and Templates, i.e. Validation Plan, Test Plan, Validation Report (German and English documentation)
04/2019 – 05/2019
Lead Auditor for IT Supplier Audit (GMP, CSV, Data Integrity)
Service Delivery and direct report to Quality Assurance and Regulatory Affairs Management
Fresenius Kabi SwissBioSimiliar, CH-Eysin
  • Auditing an IT Supplier and its Cloud Solution for Clinical Trial Analytics and Data Management (SAS): Audit Preparation, Desktop Audit (Document Review), Onsite Audit at Data Center and Quality Department, manage audit response with Supplier, create Audit Report, Audit Closure
01/2019– today
Quality and Compliance/ CSV Strategy Consultant, Laboratory Relocation
Service Delivery and direct report to Quality Assurance and Regulatory Affairs Management
Fresenius Kabi SwissBioSimiliar, CH-Eysin
  • Giving Strategy and Advice to establish a Corporate Framework for Project Governance of Computer System Validation and Equipment Qualification during Laboratory Relocation
  • Conception and Realization of Validation Strategy for the Development and Implementation of local and global IT Systems for Document Management (Documentum D2 for eTMF, eCTD, Submission Management, R&D) and Data Handling (eLN, Rotronic RMS) within the Research & Development Laboratory
01/2018– 03/2019
Global Quality and Compliance Strategy Consultant, Medical Device Software (SaMD)
Service Delivery and direct report to Managing Director Digital Lab for Software Development of Medical Device Software and Computerized Systems
Fresenius Kabi Digital Labs GmbH, Berlin
  • Conception and Realization of Software Development Framework for Digital and Mobile Solutions based on Scrum Methodology combining regulated Life Cycle Documentation of Medical Device Software Validation and Verification and Computerized System Validation
  • Validation Strategy and Management for Digital Health Medical Apps
•        Validation Concept and Management for Software Validation of JIRA and Confluence for usage as validated Project and Documentation Software within Digital Lab
  • Quality Management support to implement Quality Management System ISO 134585, ISO 27001 and ISO 9001 into Digital Labs (QMS Handbook, Procedures, Internal Audits)
  • Regulatory Compliance within Pharmaceuticals and Medical Device industry (EMA, FDA, PIC/S, ISO, MDD)
  • Quality Risk Management (FMEA)
  • Software Validation and Verification (IEC 623304/82304, GAMP 5)
  • Training and Coaching in regard to Computer System Validation and Regulatory Compliance
  • Stakeholder Management within Fresenius Quality Community
11/2017– today
Global IT Quality and Compliance Strategy Consultant, Program Quality Lead, Senior Business Analyst and Requirements Engineer
Service Delivery and direct report to Head of Global Quality and Global IT Management
Fresenius Kabi, worldwide
•        Conception and Realization of a Global Competence Center for Computer System Validation to ensure worldwide Quality Assurance and Compliance of gxp-relevant IT systems and projects, including implementation of CSV Knowledge Management and Quality Assurance Unit worldwide
•        Conception and Process Design of One Global IT Architecture Landscape for a validated Global Application Lifecycle Management, integrating all Global IT Systems through harmonized Business Process & Business Requirement Management, System Specification and Test Case Design (using ARIS BPM Tool), including Change Control and Change Impact Analysis
•        CSV/ Software Validation of ARIS BPM Tool to manage all business process/ system changes and validation documentation (URS, FS, RA, Test Scripts) within ARIS (validated Approval workflow without print outs)
  • CSV/ Software Validation of new implementation of Service Now Discovery/ IT Infrastructure
  • CSV/ Software Validation and Quality Assurance of global Archive System in compliance with Data Integrity and EU-DSGVO, creation of business requirements and SOPs/ WIs in regard to Data Integrity and ERES regulations
  • CSV/ Software Validation and Quality Assurance, Program Quality Lead of global Cloud Solution
  • CSV/ Software Validation and Quality Assurance, Program Quality Lead for Office 365 corporate Implementation and Global Rollout (Lotus Notes to Office 365), including Data Migration Projects for GxP-relevant IT System to SharePoint or Documentum D2
Global Quality Assurance and Global Program Lead for Computer System Validation
Global Quality & System Compliance, Global IT and Business Transformation, Worldwide Rollout of harmonized SAP, MES and Documentum D2
Fresenius Kabi, worldwide
  • Giving Strategy and Advice to establish a Corporate Framework for Project Governance of Computer System Validation (risk-based approach GAMP5) to Head of Global Quality and Global IT
  • Ensure the Corporate Framework and corresponding Global Operating Procedures are fully integrated into Fresenius Kabi Global IT Strategy
  • Ensure that computer system validation strategy is effectively implemented for all GxP systems and that they remain compliant throughout their life-cycle
  • Support the development of compliance standards (e.g. Global Operating Procedures, templates, and training materials) as well as IT project related documents in line with Fresenius quality and regulatory requirements in the respective IT function.
  • Liaise effectively with Quality and IT personnel across Fresenius Kabi as well as other Divisional quality and business functions to ensure that standards and effective processes for governing GxP computerized systems are in place, maintained and opportunities for continuous improvement identified and implemented
  • Support the development and delivery of training relevant for Quality, IT and business functions in the area of computerized systems compliance
  • Develop and integrate appropriate risk-based models for CSV activities of GxP systems
  • Support the development and drive the implementation of Risk Management Strategy in line with quality and regulatory requirements to ensure effective and compliant quality oversight over GxP computerized system
  • Monitor risks and deviations related to GxP computerized systems and computer system validation to ensure gaps are identified, adequately addressed and documented
  • Support throughout several project deliveries with regards to aspects of project related risk, compliance and quality
  • Track quality and compliance risks for ongoing projects, perform root cause analysis on trends and address deviations via preventive, detective and corrective measures
  • Ensure adequate analysis have been performed for relevant testing conditions based on functional risk assessment, test overview list, test plan, test results, test deviations and change requests.
10/2015 – 12/2015
IT Quality Audit Manager with focus on IT Transition, Information Governance and Risk Management
ITIL Transition and Quality Audit Project, Digital and Commercial Solutions
Novartis AG, Basel, Switzerland
  • Ensuring that the transition projects and applications are managed in compliance with IGM requirements, e.g. Novartis project management methodology (“ICE”)
  • Validating and auditing all project and system life cycle documents in compliance with IGM/ICE and CSV to force the acceptance of transition, developing document management and archiving concept for all audit relevant documents
  • Verify that all project-related tests are conducted according to the project quality plan and in compliance with IGM requirements.
  • Perform quality reviews for audit readiness, identify and document all project observations, gaps and risk with associated mitigation strategies
  • Support the problem solving of project and quality risk and provide quality guidance on GxP regulatory requirements (including, but not limited to 21 CFR Parts 11, 820 and EU GMP Annex 11.)
  • Schedule sessions with Project and Operations Team to drive mitigation actions on gaps and risks 
  • Ensure Acceptance Meetings, Knowledge Transfer and Asset identification for project transition
05/2015 – 09/2015  
Senior IT Business Analyst with focus on Requirements Engineering and Test Management 
Document Management Software Project, Artwork Operations 
Novartis AG, Basel, Switzerland 
  • Global Implementation of Documentum D2 for Document Management of Regulatory Artworks
  • Identify and create Business User Requirements within Workshops with Key Users to design the expected IT Solution
  • Design of Test Cases (PQ Testing) ensuring coverage of user requirements  
  • Authoring of Test Specifications  
  • Coordinate Test Execution with Subject Matter Experts  
  • Prepare and Conduct pre-go-live and post-go-live/ hyper care sessions tailored for the different end user groups of 800 users worldwide
12/2014 – 10/2015  
Senior IT Business Analyst with focus on Manufacturing and Logistics, IT Service Management 
Interim Management at Local IT, Manufacturing and Logistics 
Novartis AG, Basel, Switzerland 
  • Responsible for the integrated IT warehousing, material flow and distribution system environment in PharmOps Switzerland, support Unit Process and Logistics Services by leveraging global and local logistics systems such as SAP WM (ERP), MES /Werum), GISC Labeling and Material Movement Controller
  • Work closely with the business, Engineering and IT service providers to “translate” requirements and realize IT solutions through change and project management concerning application operations and projects (e.g. warehouse refurbishment, weighing & dispensing) for Achievement of modern technology and operations concepts according to industry best practice
  • Managing ITSM Service Management for achievement of service levels corresponding to industry best practice (price/performance etc.): incident, problem, service request and change management processes
  • Create solution architectures which fulfill business requirements for process execution, data capture, storage, availability and archiving
  • Integrate systems supporting logistics processes from warehouse automation to global supply chain.
  • Analyze pharmaceutical production (dispensation) and material flow processes and identify optimization potential
  • Maintain close relationships with business key-users to continuously expand & improve systems to meet future customer requirements. Align requirements with global standards.
  • Interview business partners, organize and run requirements sessions with groups of users.
  • Lead the project team in designing a “to be” process. Lead authoring of the user requirements document.
  • Ensure the business aligns processes (SOPs) with the system functionality
  • Collaborate to define deployment and business value metrics that can be used to indicate successful roll out and use of new technology.
  • Serve as SAP Change Management Evaluation Assessor and Approver (Business Owner) on behalf of the respective system owner.
  • Evaluate proposed SAP QSCRs for potential local impact and initiate necessary changes to local business processes, partner systems (interfaces), Standard Operating Procedures, Authorization roles, and Training Materials with the business.
  • Perform the local SAP Change Management process in accordance with the ACMS Change Management SOP.
  • Serve as local system manager for SAP, GISC Labeling, MMC and My Catalogue Pool (MCP)
  • Development of MS SharePoint Site for Document Management and Knowledge Base for Key Users, delivered Workshops, Trainings and Onboarding Strategy 
05/2014 – 12/2014  
Project Manager with focus on Change and Communication Management, Business Process Analysis 
Business Transformation and Transition Project, Supply Chain Excellence, MRP II Class A
Novartis AG, Basel, Switzerland 
  • Leading the Transition of Master Data Management and Purchasing from Basel/Switzerland to Hyderabad/India in Pharma External Supply Organization
  • Accompany of NOSSCEE (Novartis Operational Standards for Supply Chain Excellence), Project to establish Global Supply Chain Excellence and KPI Reporting to target a MRP2 Class-A Certification, audited by Oliver Wright Company
  • Direct reports to Head of Supply Chain and Steering Committee: project charter, project plan, project report,status reports, risk plan including targets, milestones, resources, cost, expenses
  • Business Process Analysis, Gap Analysis and Optimization 
  • Development of value-creation and harmonized processes within all involved functions: Quality, Supply Chain, Sourcing and Finance 
  • Stakeholder Management
  • Change Management, Change Communication 
  • Training Development, Training Coordination 
Achievements:  
  • Improve Business Process including KPI Reporting of Master Data Management and Operational Sourcing to handover to new Master Data Team in Hyderabad/India (Business Process Offshoring/ Outsourcing) 
  • Delivered Change and Communication Strategy including Stakeholder Management 
  • Delivered Workshops, Trainings and Onboarding Strategy for new Master Data Team in India and all effected users and stakeholders 
10/2013 – 04/2014 
Project Quality Manager Computer System Validation, Document Management Responsible
Change Control Project with Oracle Agile integration, Global Technical Operations, Supply Chain 
Novartis AG, Basel, Switzerland 
  • Implementation of an integrated system based on Oracle Agile PLM to change control and support product information management of regulatory relevant information for Pharma 
  • Preparation of key Computerized System Validation documents, such as Validation Plan and Validation Report, conducting Quality Risk Assessment
  • Coordination of the preparation of documents by adequate stakeholders 
  • Management of the review, approval and implementation process of project deliverables 
  • Definition of the Tollgate Report, tracking of Tollgate deliverables 
Achievements:  
  • Delivered Validation Strategy 
  • Delivered compliant system, no incidents 
  • Improved Project Documentation Management by implementing new concept for document archiving and approval process including Training for all writers and users 
 
05/2013 – 10/2013 
IT Business Analyst, SAP Data Migration Manager 
SAP Data Migration Project, Supply Chain Management 
Novartis AG, Basel, Switzerland 
  • Integration of API Drug Substance and SRM Strategic Raw Material business in one single SAP plant for Multimarket business and Switzerland in Pharma Supply Chain 
  • Development of the data migration methodology & implementation plan 
  • Development of best practice, processes and standards for effectively carrying out data migration activities 
  • Analysis, cleansing, harmonization and migration of data 
  • Coordination of testing activities 
  • Change Management, Change Communication 
  • Training Development, Training Coordination 
Achievements:  
  • Delivered Migration and Cutover Strategy 
  • Assessed and delivered clean and proper Data for data migration activities 
 
12/2012 – 04/2013 
Project Manager Change and Communication Management, Business Process Analysis 
Business Transformation Project with SAP SCM integration, Supply Chain Management 
Novartis AG, Basel, Switzerland 
  • Establishment of Master Data Organization in External Supply Chain Management 
  • Establishment of Supply Data Manager job role 
  • Integration of MDM Team to ESO Organization 
  • Business and IT Process Analysis and Optimization 
  • Improvement of Standard Organization Procedures including process flows 
  • Training Development, Training Coordination  
  • Change Management, Change Communication 
Achievements:  
  • Drive the organizational Change in Master Data Organization and make sure the functional solution fits to the global and local structures 
  • Delivered Change and Communication Strategy including Stakeholder Management 
  • Delivered Workshops and Trainings for users and stakeholders 
09/2012 – 11/2012 
Project Manager Supply Chain Master Data Management, Business Process Modelling and Engineering
SAP – New Plant Implementation Project, Supply Chain Management 
Novartis AG, Basel, Switzerland 
  • Implementation of a new SAP plant to concentrate all business operations for multimarket and European external supply activities in Pharma External Supply Organization 
  • Leading the Workstream for Master Data Management
  • Direct reports to Head of Supply Chain and Steering Committee: project charter, project plan, project report, status reports, risk plan including targets, milestones, resources, cost, expenses
  • Business Process Analysis and Optimization 
  • Development of value-creation and harmonized processes within all involved functions: Quality, Supply Chain, Sourcing and Finance 
  • Change Management, Change Communication 
  • Training Management, Training Coordination 
Achievements:  
  • Developed of Master Data Maintenance Strategy for Material, Vendor and Quality Master Data 
  • Delivered Concept for Master Data Governance 
 
02/2012 – 07/2012 
PMO Lead 
Various Projects 
Deutsche Telekom AG, Bonn, Germany 
  • PMO/Project Management Officer to Program Manager Product Design & Innovations, Telekom Innovation Labs, Virtualized Infrastructure & Global Cloud IT, User Experience Design 
  • Project Management for Design Transformation and Global Talent Management, Change Management, Change Communication, Concepts & Text, Design Thinking, Agile/Scrum 
Achievements:  
  • Improve Talent Management Strategy to hire worldwide the most talented Designers for Deutsche Telekom Product Design 
 
05/2010 – 05/2011 
Chief Editor/ TV-Journalism & TV-Production 
Various TV Projects 
RTL Television, Cologne, Germany 
  • TV Editorial, TV Production, Television reports, features, magazines, RTL Punkt 12, RTL exklusiv, VOX prominent  
Achievements:  
  • Developed TV-Production concept and editorial for TV-Features with ViPs like Topmodel Franziska Knuppe, Fashion Designer Talbot & Runhof and Guido Maria Kretschmar 
 
08/2007 – 08/2012 
Corporate Communication Manager, Public Relations Officer
Various Projects & Clients (Deutsche Telekom, Deutsche Post, RTL Television, Versatel, Runners Point) 
Agency for Corporate Communication and Strategy, Corporate Branding, Public and Social Media Relations, Digital Marketing and Design, Cologne, Germany 
  • Consulting for Strategy, Conception, Campaigning, Branding, Public Relations, Online & Social Media Relations, Digital Marketing, Corporate and Web Design 
  • Social Media Management, Content Management, Journalism, Editorials 
  • Event Management, Incentives 
  • Art & Culture Management, Bookings and Promotion 
Achievements:  
  • Developed Communication and Marketing strategies, that foster innovation in the digital space by adding cross-domain, cross-functional expertise on technology and business trends 
  • Reference Project: Developing and implement “VERSA” as digital avatar for VERSATEL to enforce Customer Relationship and Online Reputation Management on twitter, Facebook and diverse online forums (First Online Avatar in Germany)
 01/2007 – 07/2007 
Project Manager – Online and Digital Marketing 
Various Projects 
Virtual Nights Media Ltd, Essen, Germany 
  • Online Editorials, Internet/Intranet Content Management (TYPO 3, JOOMLA), CRM, Social Media, Festivals and Incentives, Conception, Campaigning, Branding 
Achievements:  
  • Developed Sponsoring and Communication Concept for Love Parade Dortmund and other international Events and Festivals 
  • Developed new Micro-Website for Customer Services in TYPO 3
06/2006 – 12/2006 
Project Manager – Marketing and Events 
Various Projects 
Movie Art Marketing, Dortmund, Germany 
  • Project Management, Event Management, Incentives, Sponsoring, Product Placement in TV and Cinema movie productions, Online Editorials, Internet/Intranet Content Management, CRM, Social Media, Festivals and Incentives, Conception, Campaigning, Branding 
Achievements:  
  • Increase the sells for Sponsoring and Customer Events over a 35 % during my procedure 
  • Delivered Marketing Strategy for Charity Golf Event of Deutsche Post and Kamps
01/2006 – 06/2006 
Junior Project Manager – Marketing and Events 
Various Corporate Communication & Branding, Public Relations Projects 
Evonik AG, Düsseldorf, Germany 
  • Personal Assistant to Head of Corporate Communications and Head of Public Relations, Junior Project Manager for global Projects in Corporate Communications & Branding, Public Relations 
ZEITLICHE UND RÄUMLICHE VERFÜGBARKEIT
Weltweite Reisebereitschaften
KONTAKTANFRAGE VERSENDEN

Nachricht:

Absenderdaten: