Verfügbarkeit
Verfügbar
Stundensatz
75 - 100 EUR/ Stunde
Vororteinsatz
Möglich
Standort
65812 Bad Soden am Taunus, Deutschland

Persönliche Daten

Nationalität
Schweiz
Beruflicher Status
Freelancer
Berufserfahrung
30 Jahre
Sprachkenntnisse

Deutsch (Muttersprache)

English (Fließend)

Französisch (Gut)

Zur Person

As a Dipl. Ing. Technische Informatik, I have been working in the field of IT for almost 20 years. During this time, I have gained extensive experience in the management of international teams and projects, the implementation of global IT solutions in regulated environments, the management of global IT services and system operations, and the understanding of quality and compliance processes in life science. I have also been involved in the implementation and roll-out of quality management processes and compliance solutions at enterprise level, as well as several global TRACKWISE and DOCUMENTUM implementations. Additionally, I have experience in the development of reporting solutions such as SAP BW, Crystal Reports, QLIKVIEW Reporting, Trending & Management Reporting. I am confident that my experience and qualifications make me an ideal candidate for any project requiring the management of international teams and projects, the implementation of global IT solutions in regulated environments, the management of global IT services and system operations, and the understanding of quality and compliance processes in life science. If you are looking for a reliable and experienced Dipl. Ing. Technische Informatik, please do not hesitate to contact me. I am available to discuss any project requirements and look forward to hearing from you. Send Request Now.

Beschreibung

* Management of International Teams and Projects Implementing Global IT Solutions in Regulated Environments, since 2001 (PMI, GxP, SoX)
* Management of Global IT Services and System Operations, since 2001 (ITIL), in Regulated Environments (FDA, EMEA, BfArM) since 2005
* Excellent Understanding of Quality and Compliance Processes in Life Science (API, Pharmaceutical & Medical Devices)
* Strong Experiences in Managing Implementations & Roll-outs of Quality Management Processes and Compliance Solutions at Enterprise Level, since 2006
* Several global TRACKWISE Implementations, since 2005 (CAPA, Deviations, Change, Complaints, Adverse Event Reporting, eMDR, Supplier Quality, Audit & Risk Management)
* Several global DOCUMENTUM Implementations, since 2005 ( SOP/ Procedures, Quality Records, Master Batch Records, Non-GxP Documentation, eROOM)
* Several Reporting Solutions, since 2001 (SAP BW, Crystal Reports, QLIKVIEW Reporting, Trending & Management Reporting)

Referenzen

03/2009 - heute(15 Jahre, 2 Monate)
GAMBRO Renal Products
IT Leiter, Global Applications ECM & Quality
03/2005 - 02/2009(4 Jahre)
Sanofi, Industrial Operations
IT Manager, Global Document and Quality Solutions
12/2001 - 02/2005(3 Jahre, 3 Monate)
Aventis Pharma AG
IT Manager, Global Support eProcurement
01/2001 - 11/2001(11 Monate)
Deloitte Consulting
Senior Consultant, B2B Buy Side
06/1999 - 12/2000(1 Jahr, 6 Monate)
HP Consulting
Consultant, eProcurement Solutions
10/1995 - 05/1999(3 Jahre, 8 Monate)
Hewlett Packard, Test & Measurement
Sales Engineer

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Statistik von Kai Kiefer

Mitglied seit 13.10.2012
1459  Profilaufrufe
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PERSONAL:

Dipl.-Ing. (BA) Technische Informatik
Joseph-Haydn Strasse 26b
D - 65812 Bad Soden

[email protected]

+49.151.226.57576

OBJECTIVES

Challenges, Software & IT Services
Regulated Businesses / Life Sciences
Working in International Environment

KEY 
COMPETENCIES

Management of International Teams and Projects Implementing Global 
IT Solutions in Regulated Environments, since 2001 (PMI, GAMP, SoX)

Management of Global IT Services and System Operations, since 2001 
(ITIL), in Regulated Environments (FDA, EMEA, BfArM) since 2005

Working in International Environments, since 1995

Excellent Understanding of Quality and Compliance Processes in Life 
Science (API, Pharmaceutical & Medical Devices)

Strong Experiences in Managing Implementations & Rollouts of Quality 
Management Processes and Compliance Solutions at Enterprise Level, 
since 2006 

o

Several global TRACKWISE Implementations, since 2005 (CAPA, 
Deviations, Change, Complaints, Adverse Event Reporting, eMDR, 
Supplier Quality, Audit & Risk Management)

o

Several global DOCUMENTUM Implementations, since 2005 ( SOP/ 
Procedures, Quality Records, Master Batch Records, Non-GxP 
Documentation, eROOM)

o

Several Reporting Solutions, since 2001 (SAP BW, Crystal Reports, 
QLIKVIEW Reporting, Trending & Management Reporting)

ARIBA Purchasing/Invoicing Solutions Implementations (Indirect 
Procurement, Contract Management, Tender/Quotation Management, 
Reverse Auctions) from 1999-2004

HISTORY

Manager, IT Center of Excellence ECM & Quality Solutions

GAMBRO Renal Products, Medical Devices 
March 2009 - today

Responsible for IT Applications and Platforms, 2 Teams, 6 people 
located in Sweden and Hechingen, 

o

Global Quality Management Solution Platform, used worldwide for 
Post Market Surveillance, CAPA and Audit Management. 700 users

o

12 Enterprise Content Management Platforms used worldwide for 
Collaboration, Publishing, Doc Control, Labeling, Contract 
Management, 1500 users

o

Global eLearning Service, used worldwide with 2500 users

o

IT Solutions supporting Clinical Trails

Technologies:
DOCUMENTUM, TRACKWISE, QLIKVIEW, eROOM, SHAREPOINT, 
JAVA, .NET, XML, AS2 Messaging, MSSQL, MICROSOFT SERVERS

Curriculum Vitae - KAI KIEFER

Curriculum Vitae - KAI KIEFER

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HISTORY

Achievements:

o

Established Center of Excellence for Content Management and 
Quality Solutions, aligned Cooperate IT and Quality and Business 
Functions, transitioned technical solutions to Center of Excellences, 
build up team and services for support and projects

o

Defined an overall Quality/IT Alignment Strategy, established 
Enterprise Architecture, Process and Technology Landscape. 
Established overall Program Road Map, Management of 
Implementation and Roll-outs of First Phase Projects.

o

Implemented full cycle Post Surveillance Solution (Complaints, Field 
Actions, Adverse Event Reporting, Management Product Review)

o

Established Global IT standards for Software Validation, System 
Operation and Change Control (based on GAMP5 and ITIL v3)

o

Supported Quality Organization during various FDA Inspections as 
System Owner

o

Given Public Speeches on Quality Management and Document 
Management 

IT Manager for Global Document and Quality Management 
Solutions

Sanofi Aventis, Pharmaceutical Industry
March 2005 – February 2009 

 

Responsible for several  IS Applications and Platforms, 10+ projects/
year, 2 Project Teams, 15+ people located in Frankfurt and Paris, 
yearly Budget >5M$

o

Global Document Management Platforms for controlled Documents 
and non-controlled Documents , 6000+ trained users, used with in 
25 Sites, globally 40.000 signatures/month, integration with local 
ERP Systems

o

Global Quality Process Platform Processes: Supplier Audits, Risk 
Management, Deviation Management, eCAPA and Change Control) 
for currently 1500 users used in over 80 sites.

o

Automated Functional Testing, IS Change control, IS Incident 
Management, IS Release Management System

Technologies:

DOCUMENTUM 5 & 6, ADOBE, TRACKWISE, CRYSTAL REPORTS, 
SERENA DIMENSIONS, HP/MERCURY QUICKTEST,JAVA, HP-UX, 
WINDOWS 2003, ORACLE DB

Achievements:

o

Build up Support and Project teams, developed and implemented 
mid-term and long-range project and budget plans

o

Coordinated and managed Roll-out Program with over 30 Sub 
projects, managed several Data Centre Migrations (3), and 
migration several major(5+) and minor(10+) Software releases and 
Upgrades, Managed Migration and Integration of several existing 
solutions into global platforms

o

Ensured Development and Support Process being audible and 
conform with internal Quality Standards, defended operations 
against internal and external audits, Optimized internal Processes 
according to industry best practices (ITIL, GAMP, TQM, PMBOK) 
Actively driven relationships with Software Vendor and Sanofi-
Aventis Industrial Affairs

Curriculum Vitae - KAI KIEFER

Curriculum Vitae - KAI KIEFER

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HISTORY

o

Implemented Integrated version, build & release management 
Solution

o

Implemented Support Delivery Process Solution 

o

Developed several automated Functional Testing Programs

IT Manager – Global Support e-Procurement Solution 

Sanofi Aventis, Pharmaceutical Industry
December 2001 – February 2005

Responsible for operation and support of an Global e-Procurement 
Platform 
 20.000 users, integrated with 18 SAP system in 24 countries, Team 
with 10+ people located in France, US and Germany
ARIBA BUYER & SOURCING, TIBCO, SAP, JAVA, HP-UX, ORACLE, CFT

Achievements:

o

Build up and established a global 24h Support organization 

o

Managed established SLAs and managed Services Delivery 
according to agreements and KPIs (based on ITIL Framework)

o

Coordinated and managed several Go-Lives and Migration 
Activities

o

Setup up and implemented Quality Improvements and Efficiency 
Programs 

o

Organized and performed Workshops for technical ARIBA 
SOURCING

o

Actively driven Supplier Relationship 

Senior Consultant, B2B Buy Side Technology

Deloitte Consulting, Management Consulting Industry
January 2001 – November 2001 

Support Global Purchasing in Supplier Integration Process to 
eProcurement Platform (ARIBA BUYER) Netherlands

Lead Internal Education Program and Sales Awareness Activities

Performed Software Cost Estimation for Banking Software

Consultant, e-Procurement Solutions

Hewlett Packard,  Information Technology and Services Industry
June 1999 – December 2000

Support Sales & Marketing Activities for TOP 100 HP European 
Clients (ARIBA)

Conduct Presentations, Public Speeches and Workshops

Developed and Maintained a global eCatalog Publishing Application

2 month support Internal Roll-out Activities and Supplier Adoption 
Projects ( Palo Alto / CA)

3 month intense ARIBA Train the Trainer Program in Sunnyvale, CA

Sales Engineer - Electronic Test & Measurement Products

Hewlett Packard, Electrical/Electronic Manufacturing Industry
October 1995 – May 1999 

Consulting customers on using Electronic Test  & Measurement 
Tools (D/A/CH)

Support Fairs, Presentations and Road shows (D/A/CH)

In-house Telesales activities (Germany)

2 months stay in Mountain View, CA for T&M University 

Curriculum Vitae - KAI KIEFER

Curriculum Vitae - KAI KIEFER

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HISTORY

Seed Student

Hewlett Packard, Electrical/Electronic Manufacturing Industry
October 1992 – September 1995

2 months stay in Colorado Springs / CO, during Senior Project

EDUCATION

1992 – 1995 Berufsakademie Stuttgart, Computer Science

Dissertation: “Embedded Debugging Concept for a Siemens Micro 
Controller Family”,  Grade 1.0

1994 Staatl.-geprüft. Mathematisch Technischer Assistent

1992 Werner-Siemens Schule,Stuttgart,  
          Allgemeine Hochschulreife, Grade Average 1.9

1992  Staatl.-geprüft. Technischer Assistent Nachrichten Technik
1989  Fachschule Reife – Berufsfeld: METAL, Award
1987  Hauptschulabschluss , Award

QUALIFICATIONS

Languages

German - mother tongue

English - fluent

French - intermediate

Skill Trainings

CERTIFIED COMPUTER VALIDATION MANAGER 

ITIL Infrastructure in Regulated Environments

IT-Service Management with ITIL

HP Strategic Visioning, HP Effective Presentation, HP Effective Sales

HP Test & Measurement Sales Engineer

Technology Trainings

ARIBA BUYER Train the Trainer Certificate 

DOCUMENTUM Compliance Manager 5 

TRACKWISE Configuration & Utilities

ARIBA BUYER 7.0 Customization

SERENA DIMENSION CM 10 Administration and Configuration

HP QUICKTEST PROFESSIONAL Basic and Advanced

QLIKVIEW Developer

PRIVATE 
INTERESTS

Sports

Swim/Bike/Run & Triathlon

Volleyball

WindSurfing

Music 

Guitar (Blues/Pop)

Piano

Curriculum Vitae - KAI KIEFER

Curriculum Vitae - KAI KIEFER