MedTech Safety & Quality & Requirements & Usability & Risk Manager-Engineer/ Team-Project Lead/ SYS & SW & HW Architect
Aktualisiert am 13.12.2023
Profil
Referenzen (2)
Freiberufler / Selbstständiger
Remote-Arbeit
Verfügbar ab: 13.12.2023
Verfügbar zu: 100%
davon vor Ort: 100%
Requirements Engineering
Teamleading
Risikomanagement
Künstliche Intelligenz
Data Scientist
FMEA
Algorithmics
Projektmanagement/Projektleitung
Systems Engineering
SystemArchitektur
CVS
DIN 13485
ISO 14971
IEC 62304
IEC 62366
Machine Learning
German
Business level/ fluent
English
Business level/ fluent
Italian
Business level/ fluent
Spanish
Mother tongue
Valencian/ Catalan
Mother tongue
Russian
Basic
Swedish
Basic
French
Basic

Einsatzorte

Einsatzorte

Deutschland, Österreich, Schweiz

Weltweit ansetzbar. Aber am besten wäre gleich in Valencia oder in Frankfurt, oder in der Nähe. Oder in Osteuropa Oder USA.

möglich

Projekte

Projekte

2023: ARTIFICIAL INTELLIGENCE, MACHINE LEARNING & DATA SCIENCE

Role: ARTIFICIAL INTELLIGENCE, MACHINE LEARNING & DATA SCIENCE ENGINEER / CONSULTANT / COACH / ADVISOR
Location: Germany & Remote
Customer: Start-Up

Tasks
  • Machine Learning/ Algorithmics/ Data Science/ Artificial Intelligence/ Big Data/ Neural Networks/ Deep Learning/ Software Architecture & Design/ Framework Concept & Development/ DevOps/ Programming/ Requirements Engineering-Management

Skills:
Python & R/ Anaconda/ PyTorch/ TensorFlow/ Scikit-Learn/ Zeppelin & Jupyter Notebooks/ ONNX AI/ Gitlab CI/CD/ DVC (Data Version Control)/ SQL/ SCRUM/ Agile/ Kubernetes/ Docker/ HADOOP/ Amazon AWS/ Value Cloud/ Celery/ DJANGO/ React ?JavaScript/ REST APIs/ GitOps/ Argo CD/ SysML/ UML/ BPMN/ JIRA/ Confluence


2022 - 2023: QUALITY MANAGEMENT/ COMPUTER SYSTEM VALIDATION/ GAMP 5 CSV/ SOPs & WIs/ PLANNING/ BPMN/ TEST MANAGEMENT

Role: SYSTEMS ENGINEER/ QUALITY MANAGEMENT/ COMPUTER SYSTEM VALIDATION/ GAMP 5 CSV/ SOPs & WIs/ PLANNING/ BPMN/ TEST MANAGEMENT
Location: Germany & Remote
Customer: BioNTech SE (PHARMA)

Tasks
  • Pharmaceutical Development & Production/ Digitalization of Paper-Based Pharmaceutical Manufacturing Process/ IQ (Installation Qualification)/ OQ (Operational Qualification)/ PQ (Performance Qualification)/ Databases/ GAMP5 CSV (Computer System Validation)/ SAP Cutover Planning and Execution/ Documentation Approvals/ Regulatory Affairs/ Write & Review SOPs (Standard Operating Procedures) & WIs (Working Instructions)/ SCM - Supply Chain Management Testing/ Test Management/ Quality Control/ Quality Management/ Clinical Trials/ SAP Introduction in the company/ Multi-site/ SW
  • ERP Tool Change Cutover Planning and Execution / SW Tool Deployment (SAP ERP in Supply Chain Mgmt) / FMEAs / BPMN 2.0 (Business Process Model and Notation) / BPM (Business Process Management) / ADONIS BPM Suite / Risk Management / Ris Assessments / FMEAs / FTAs / HAZOP / Corona Virus Vaccine / individualized Neoantigen/mRNA/cancer Specific Immunotherapy (iNeST) / Monoclonal Antibody Therapies (Cancer, etc)
  • Pharma Product / Pharmaceutical Production / IFUs (Instructions for Use) & O&M (Operation & Maintenance Manuals) / Systems Engineering / Documentation / Training / DMSs SOP-Guard & SOP-Form/ Software / Audit Trials / Changes / Databases / SQL / CAPAs / V-Model & SCRUM

Skills:
MS Office/ Adonis BPM/ GUS-OS ERP/ SAP ERP/ SOP-Guard/Alpega TMS/ MS Navision/ WinSped/ MS Teams ? Sharepoint/ LabWare LIMS & ELN/ MES


2022: RISK & QUALITY MANAGEMENT

Role: RISK MANAGER/ QUALITY MANAGEMENT/ FMEA MODERATION & ISSUANCE/ TEAM LEADING/ COORDINATION/ SYSTEMS ENGINEERING
Location: Germany & Remote

Tasks
  • RISK & QUALITY MANAGEMENT, Artificial Intelligence, Machine Vision & Sensor R&D
  • APIS IQ-RM Pro / DOORS / JIRA/ Medini Analyze / PTC-MKS Integrity/ Enterprise Architect
  • FMEA Issuance and Moderation (SYS/SW/HW/MD)/ Team Leading/ Coordination/ Systems Engineering/ Risk Management/ Requirements Engineering / Quality Management/ Documentation/ Coaching-Training/ Safety Related Hardware, Mechanical Design, Software and System Level FMEAs / FTAs / Safety Analysis / C-C++ / VB.NET


2020 - 2021: various projects

Role: TEAM LEAD/ REGULATORY AFFAIRS/ SYSTEMS ENGINEERING (+SW+HW+MD)/ RISK MANAGEMENT/ QUALITY MANAGEMENT/ REQUIREMENTS MANAGEMENT/ ALM- PLM CONSULTANT
Location: Ireland & Remote
Customer: MALLINCKRODT Pharmaceuticals (PHARMA & MedTech & Combination Products)

Tasks
  • 2 projects: Nitric Oxide pulmonary Delivery System (China registration) & Extracorporeal blood Photochemotherapy (ECP)/ Photopheresis System
  • Documentation Review and Approval, FDA & China & EU Submissions, PMAs/ IDEs/ 510Ks, Systems Engineering, Regulatory Affairs, Risk Management, Quality Management Quality Management, Documentation, Audits, Cross functional interfacing (Medical, Clinical, V&V, company management, Usability, RA, Legal, Marketing, Purchasing, Engineering, Quality, Risk Mgmt), stakeholder management, ALM/PLM Consultancy & Planning & Implementation, Systems Engineering, Requirements Engineering/Management, System Architecture, Software, Risk Management, Quality Management, Documentation, Reviews. DMS, V-Model, Microsoft Project, Enterprise Architect/EA/SysML/UML, JAMA ReqEng, listing of international standards, resource planning, budgeting, regulations and guidelines applicable to the project (including the conversion of clauses into design input requirements), gap analysis.
  • Phases: Planning, Development, Qualification & Post-Martket

Skills
ISO 13485:2016, 21 CFR/FDA, ISO 9001, MDD/IVD, MDR/IVDR, ISO 14971, EN 62304, EN 62366, CSV, GxP, GMP, GCP, GLP, GAMP, MES, LIMS. V-Model, SCRUM, Agile, Python, JAVA, JavaScript


2020: Development and Clearance of a fully integrated Operating Theater for an Operating/ Surgery Hospital Room

Role: TEAM LEAD/ SYSTEMS ENGINEERING/ QUALITY MANAGEMENT/ RISK MANAGEMENT/ GAP ANALYSIS
Location: Germany & Remote
Customer: KARL STORZ SE & Co.KG (MedTech)

Tasks
Functions: ALM-PLM Consultancy & Planning & Implementation, Systems Engineering Leading/ Risk Management Engineering/ Regulatory Affairs Support/ DMS/ Clearance Support

Skills:
Databases, SQL, VB.NET, JAVA, Labview, C# & Testing tools, Linux OS, RTLinux OS, Siemens Polarion & Teamcenter ( ALM ? PLM ) / FDA & EU Submissions, OOD, OOP, Video Processing, Streaming, Network protocols, SaMD (Software as a medical device), IEC 60601, MDD/IVD, MDR/IVDR, ISO 14971, AAMI TIR32, AAMI TIR57, 21 CFR 820, ISO 13485, IEC 6230, SysML, V-Model, Scrum, Agile


2019 - 2020: MEDICAL DEVICES & PHARMA

Role: LEAD AUDITOR/ QUALITY MANAGER
Location: Switzerland, France, Hungary and UK + Germany & Remote
Customer: HAEMONETICS (PHARMA & MedTech & Combination Products)

Tasks
  • Blood Filtering Systems, Blood & Plasma Collection Systems & Blood Management Systems
  • SOFTWARE & HARDWARE/ Quality Management/ Several Audits as Lead Auditor/ 1st and 2nd party Audits of Medical Device/ Pharma/ Combination Products companies, Supplier Audits, Internal Audits, mock-up Audits (CE Marking, MDSAP, preparation for Notified Body Audits)

Skills
ISO 13485:2016, MDSAP, GMP, GCP, GLP, GAMP 5, SaMD (Software as a Medical Device), 21 CFR/FDA, ISO 9001, MDD/IVD, MDR/IVDR, ISO 14971, EN 62304, EN 62366


2017 - 2018: Development and Market Clearance (especially USA/FDA and EU) of different Insulin Infusion Pump Systems/ Auto-injectors & Pens/ SaMD (Software as a Medical Device)

Role: QUALITY MANAGEMER/ REGULATTORY AFFAIRS/ RISK MANAGER/ SAFETY ASSURANCE CASES LEAD
Customer: YPSOMED & ROCHE DIABES CARE (PHARMA & MedTech & Combination Products)
Loctation: Germany & Switzerland & Remote

Tasks
  • MEDICAL TECHNOLOGIES (Class 2 device) and PHARMA (Combination Products)
  • Function: Regulatory Affairs Support/ Clearance Support/ Post-market/ Clinical Evaluation/ Clinical Trials/ Risk Manager/ Risk Assessments/ Supplier Management/ Safety Assurance Cases/ Quality Engineer/ Requirements Engineer
  • Goals: Engineering Lead/ FDA & EU Submissions (PMAs/510Ks/IDEs/CE-Mark)/ Resource planning/ Introduction of Software tools in the company/ Coordination of external partners and internal teams/ Budgeting/ Risk Management/ ALM-PLM
  • Consultancy & Planning & Implementation/ CSV (Computer System Validation)/ DMS/ Perform Safety Assurance Cases (SACs) ? including Cyber-Security -, SIEMENS MES, SIEMENS Opcenter, DMS, Labware LIMS, Preliminary Hazard Lists and Analysis, Risk Analysis, FTAs and FMEAs; DHF, DMR & DHR; SACs: in the case of insulin pumps, based on ?Infusion Pumps Total Product Life Cycle, Guidance for Industry and FDA Staff? (December 2, 2014)
  • RIMS/ Additional norms/ guidances/ papers applied/used: Papers on cybersecurity, ISO 14971/ ISO 15026/ MDD, MDR/ AAMI TIR32/ AAMI TIR57/ 21 CFR 820/ ISO 13485/ LIMS Labware/ IEC 62304/ IEC 60601/ WiFi/ Audits
  • Listing of international standards, regulations and guidelines applicable to the project, conversion of clauses into design input requirements (including assessment), gap analysis
  • Additional Tasks: CAPAs, interaction with the development and Regulatory Affairs teams; introduction of an appropriate SW tool for SAC performance; support of the introduction of the SAC work product and process into the company lifecycle; Cyber-Security; compilation of the Risk Management File (RMF)

Skills:
Java, JavaScript, Python, Angular & Testing tools/ V-Model, Agile, Scrum, UML, SysML/ LabWare LIMS & ELN, MES SAP, Siemens Polarion & Teamcenter (ALM ? PLM), Google Cloud/ Databases/ SQL, Polarion, DOORS, Turbo-AC, SaMD (Software as a medical device), GLP, GxP, Papers on cybersecurity, transition MDD/IVD to MDR/IVDR, GAMP5, Computer System Validation (CSV)


2016 - 2017: Submission & Audit & Development & DHF (Design History File) Remediation

Role: SYSTEMS ENGINEER/ QUALITY MANAGEMENT/ GAP ANALYSIS/ REGULATORY AFFAIRS/ COORDINATION/ TESTING
Customer: ZIMMER BIOMET (MedTech)

Tasks
minimal-invasive surgery robot (electro-mechanical device) - innovative highprecision brain & spine SURGERY
  • MEDICAL TECHNOLOGIES (Class 2b device)
  • SaMD (Software as a medical device), FDA 510k submission, 93/42/EEC, FDA & EU
  • Submissions, transition MDD/IVD to MDR/IVDR, 2007/47/EC, GAMP5, Java, JUNit, Labview, SAP, C#, Matlab Simulink, C++,Perforce, GLP, GxP, CSV (Computer System Validation), 93/42/EEC, 2007/47/EC, 2016/MDR (Medical Device Regulation), Regulatory Affairs/ Project Management/ DMS/ Clearance Support/ Systems Engineering/ Risk Management/ RIMs/ Quality Engineering/ Testing/ Post-market/ Clinical Evaluation/ Clinical Trials/ EN

Skills
ISO 13485(Quality Management), EN ISO 14971 (Risk Management), EN 62304 (Software Lifecycle), Usability (EN 62366 & EN 60601-1-6), FDA 21 CFR parts 820, 803 and 806


2014 - 2016: SAFETY CRITICAL SYSTEMS

Role: PROJECT MANAGER/ SYSTEMS LEAD/ RISK MANAGER/ FUNCTIONAL SAFETY MANAGERENGINEER/ TEAM LEAD
Location: GERMANY & Remote

Tasks
  • Audits, Presentations, coaching of development; checklists, templates and process definition
  • FMEA (and FMEDA) Issuing&Moderation, Java, Javascript, Labview, C#, Matlab Simulink, C++
  • Depending on the project, responsible, author, coordinator, reviewer and/or co-authour of different work products or responsible for the whole FuSa
  • Lifecycle: Hazard%Risk Analysis, Safety Concepts, FuSa effort estimation, customer contact, Functional Safety Plan, Impact Analysis, FMEA, FMEDA, FuSa Test Specs, Safety Case, FuSa Assessments, etc.

Skills:
Medini Analyze, APIS IQ, PTC Integrity and ReqEng, Subversion, MS Project, IBM DOORS, Enterprise Architect, MS Visio, Power Point, Excel


2013 - 2014: Audits/ DHF Remediation activities / Gap Analysis, Gap Assessment and Gap Closing

Role: SYSTEMS ENGINEER/ REGULATORY AFFAIRS/ QUALITY MANAGEMENT/ AUDITS/ SYSTEM ARCHITECTURE/ REQUIREMENTS ENGINEERING
Customer: B. BRAUN (PHARMA & MedTech & Combination Products)

Tasks
Audits/ DHF Remediation activities / Gap Analysis, Gap Assessment and Gap Closing
  • Planning and Execution / FDA-clearance (PMAs/510Ks) and improvement of existing Infusion Pump Systems
  • Function: Requirements Engineering/ Regulatory Affairs Support / Clearance Support/ Postmarket / Clinical Evaluation / Clinical Trials / System & Sw Senior Quality & Design Engineer/ Requirements Management/ V-Model / Agile / SCRUM / SysML

Skills:
DMS, Polarion, Supplier Management , RIMS, 21 CFR 820/ ISO 13485/ ISO 14971/ IEC 62304/ IEC 60601/ SIEMENS MES, SIEMENS Opcenter/ WiFi/ FDA clearance-approval process - FDA 21 CFR 803/ Cybersecurity/ CSV/ STARLIMS/ GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GLP/ GCLP/ GDP/ FDA 21 CFR 806/ Total Product Life Cycle, test case/ DHF, DMR & DHR/ Audits/ CAPAs/ Optics/ SQL, Java, JavaScript, GLP, GxP, CSV (Computer System Validation)


2012 - 2013: IVD Device - New Development of the to date highest throughput medical in-vitro diagnosis for different diseases (COVID, HIV, Hepatitis, etc.) based on PCR technology

Role: REQUIREMENTS ENGINEER-MANAGER/ QUALITY MANAGEMENT/ SCRUM MASTER/ TESTING/ RISK MANAGEMENT/ QUALITY CONTROL/ DEVELOPMENT ENGINEER
Customer: ROCHE Diagnostics (MedTech & PHARMA)

Skills:
Audits/ HL7/ LIMS/ C#/ Scrum/ V-Model/ Google Cloud/ Databases/ SQL/ ISO 13485/ ISO 14971/ IEC 62304/ IEC 60601/ EU & FDA clearance approval process/ FDA 21 CFR 820/ GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GLP/ GCLP/ GDP/ FDA 21 CFR 803 & 806


2011 - 2012: SW DEVELOPMENT FOR FUNCTIONAL SAFETY

Role: TECHNICAL PROJECT MANAGER (Engineering Product Leader - EPL), RISK MANAGER, FUNCIONAL SAFETY PROJECT LEAD and TEAM LEADER OF THE FUNCTIONAL SAFETY SW-DEVELOPMENT TEAM
Location: Southern Region, GERMANY. (/remote)

Tasks
  • MS Project, IBM DOORS, MS Visio, MS Power Point, MS Excel, Atlassian JIRA & Confluence, Enterprise Architect/ ISO 26262, Automotive SPICE, AUTOSAR 4, FlexRay, CAN, Python
  • Engineering Project Manager (composed of HW-Team, SW-Team, Mech-Team, Test and Validation Teams, ?), team of ca. 60 people. Multi-cultural and multi-location team (6 locations in different countries)
  • Audits, Functional Safety (ISO 26262) project leader (HW+SW) & Team Leader/ Functional Owner of the FuSi-SW-Development team (ca. 8 people)
  • Multi-location/ remote team (4 locations)

Skills:
C, C++, VxWorks OS, DSP, CppUTest


2011: QUALITY MANAGEMENT/ QUALITY ASSURANCE TEAM LEAD/ ASSESSMENT PREPARATION

Role: Multisite (& multi-country) Team Leading
Location: GERMANY & Remote

Tasks
  • Audits, MS Project, MS Power Point, IBM/Telelogic Rational DOORS
  • Multisite (& multi-country) Team Leading
  • Goal of the Project: Process Improvement of a multi-site development as preparation for an Assessment
  • Disciplines: Requirements Management, Version Control Management, Change Management, Software Development and Testing
  • Typical Tasks: organization of meetings and workshops (with engineers, quality managers and discipline managers), chair meetings, prepare presentation slides, hold presentations, write down minutes, hold presentations and trainings, slide preparation,business trips to sites in other countries, project planning, process analysis, coordination, arrive to agreements among the different teams, commissioning, Action Item List creation and management / C, C++, VxWorks OS, Microcontrollers


2010 - 2011: SAFETY CRITICAL SYSTEMS

Role: SOFTWARE DEVELOPER/ TESTER/ REQUIREMENTS ENGINEERING/ SW DESIGN & ARCHITECTURE
Location: Northern Region, GERMANY & Remote

Skills:
Video-processing, DSP, OpenGL, Adobe Video libraries, C, C++, Qt, Microsoft Windows RT OS, Perl , PerlUnit, Test::Unit, Python, UnitTest++, QtTest


2010 - 2011: Precision electronic system for liquid-powder mixing

Role: REQUIREMENTS MANAGER -HP QUALITY CENTER- AND SYSTEMS & SW ARCHITECT
Customer: METTLER-TOLEDO (MedTech), SWITZERLAND

Tasks
Precision electronic system for liquid-powder mixing to be used in the Pharma
  • Industry and Medical Research/ Cybersecurity/ CSV/ LIMS/ DMS/ GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GLP/ GCLP/ GDP/ LabWare LIMS/ Test Case Derivation, Development, Execution and Reporting/ SIEMENS MES, SIEMENS Opcenter/ V-Model/ Agile/ SCRUM
  • PHARMA/ MEDICAL TECHNOLOGIES/ WiFi / PRECISION MEASUREMENT ELECTRONICS
  • Function: Audits/ Requirements Engineering/ Regulatoy Affairs Support/ Clearance Support/ Post-market/ Clinical Evaluation/ Clinical Trials/ System & Sw Senior Quality & Design Engineer/ Requirements Management


other projects on request

Aus- und Weiterbildung

Aus- und Weiterbildung

2002
Master?s Degree (5-years worldwide-accepted University program) in Telecommunications Engineering ? Specialties Electronics & Telecommunications, UPV Valencia, Spain

Certifications/ Trainings
  • MEDICAL TECHNOLOGIES, MEDICAL DEVICES, Biotech : AUDIT-GARANT (Advanced Professional Program for Medical Device Development and Clearance Process (Regulatory Affairs, Quality Mgmt, Technical Documentation and System Development: 47/EC, MDR, 510k, ISO 13485, ISO 14971, EN 62304, EN 62366, EN 60601-1-6, 21 CFR, HL7, DICOM, LOINC, GxP), Johner Institute
  • Different trainings on PHARMA & BioTech: GMP, GAMP5 Computer System Validation (CSV), User Requirements (URS) and Functional Specifications (FS) Definition, Risk Analysis&Management, Change Control, different DMSs (Document Management Systems), CAPAs and Action Management, ERPs and Supply Change Management and Warehouse Management Systems (SAP,GUS, etc)
  • Medical Devices LEAD AUDITOR Certification - bsi Group (Notified Body, British Standards Institution), 5 days, Frankfurt, Germany (ISO 19011:2018 / ISO 13485:2016)
  • MDSAP Auditor Training (Medical Device Single Audit Program) ? bsi Group (Notified Body, British Standards Institution), 2 days
  • INCOSE CSEP Systems Engineering Professional Certification Training
  • Certified Requirements Manager ? IREB
  • FMEA moderator Training (4 days) - KVP Institut
  • Certified Risk Manager (TüV Nord)
  • IVDR Trainings
  • MDR (Medical Device Regulation) Implementation for CE-Marking ? Training Course - bsi Group (Notified Body, British Standards Institution), 3 days, Frankfurt, Germany
  • Clinical Trials/ Clinical Studies of Medical Products. 2 days training, June 2018, Bonn/ FORUM Institut für Management
  • 3-day hands-on training about Safety Assurance Cases for Medical Devices - GessNet
  • Certified Auditor (ISO 13485:2016) ? Johner Institut, Germany
  • LIMS trainings
  • BPMN (Business Process Model & Notation) & ADONIS BPM & ADOIT Suite Training, 2 days
  • Several days of individual Training&Coaching in Project Management, Presentation, Interaction, Time Management and Rhetoric skills, techniques and tools
  • isQI CPMS (Certified Professional for Medical Software) ? currently Exam preparation
  • iSQI ISTQB Certified Tester, currently Exam Preparation

Position

Position

  • SYSTEMS ENGINEER/ REQUIREMENTS MANAGER (Customer & System & HW & SW Reqs)/ System & HW & Software ARCHITECT/ MedTech, Pharma and Biotech SENIOR ENGINEER
  • TEAM LEAD/ PROJECT MANAGER/ PM/ Scrum Master/ Scrum Product Owner
  • AI (Artificial Intelligence)/ ML (Machine Learning)/ Data Science/ Algorithm Engineer
  • RISK MANAGER (MedTech, Pharma, Biotech and Combination Products)/ Functional Safety Engineer & Manager
  • QUALITY MANAGER/ LEAD AUDITOR/ REGULATORY AFFAIRS/ Technical Documentation
  • FMEA (also FMEDA) Issuer/ Moderator
  • Software Development/ Programming
  • TESTING/ Quality Assurance/ Validation/ CSV ? Computer System Validation / Verification/ Test Management
  • HW Development/ Mechanical Design

Kompetenzen

Kompetenzen

Top-Skills

Requirements Engineering Teamleading Risikomanagement Künstliche Intelligenz Data Scientist FMEA Algorithmics Projektmanagement/Projektleitung Systems Engineering SystemArchitektur CVS DIN 13485 ISO 14971 IEC 62304 IEC 62366 Machine Learning

Produkte / Standards / Erfahrungen / Methoden

Actano RPLAN e3
AUTOSAR 4
C++ Standard Template Library (STL)
CAN
Embedded OpenGL
for C++
Ethernet
FireWire
FlexRay
MATLAB
for C
Microsoft Team Foundation Server (MS TFS)
Mindjet MindManager
MOST
MS Office
Word, PowerPoint, Excel, Access, Visio
MS Project
OpenOffice
PERL
for C
SAP
SysML
UML

Professional Experience

  • More than 10 projects in the fields of MEDICAL TECHNOLOGIES, MEDICAL DEVICES, BIOTECH, PHARMA and combination products. More than 20 years of professional experience in international teams, mainly in Germany and Switzerland, but also in Ireland, the USA, the UK, Spain, France, Italy, Romania, Austria and Hungary, as well as with various teams in Sweden, Mexico, Egypt, Israel, Australia and Asia (China, South Korea, India, Philippines and Japan).
  • Other end customers and employers in other business areas: CERN (European Organisation for Nuclear Research)
  • Additional Know-How in Pharma, BioTech, Biomedicine & Biology ? Cancer, Aging, Longevity, Omics ?Genomics, Epigenomics, Proteomics, Transcriptomics, Metabolomics-, Lab-grown organs, etc (Research, Services, Products, Networking, etc)
  • Several Audits: supplier Audits, internal Audits, mock-up Audits (ISO 13485, MDSAP, GCP, GMP, GAMP 5, GLP, GxP, FDA 21 CFRs, FDA 21 CFR 58, ISO 9001, ISO 14971, EN 62304, EN 62366, EN 60601, EU/ MDD/ MDR/ IVDD/ IVDR, USA/FDA, Canada/HC, Australia/TGA, Brasil/ANVISA, Japan/MHLW, etc)

SKILLS & TECHNOLOGIES
  • Applied and theoretical knowledge of MEDICAL TECHNOLOGIES/ PHARMA/ BioTech Specifications and Laws/Regulations: Design, Quality, Regulatory Affairs, GxP, GMP, GCP, GLP, GAMP 5, CSV (Computer System Validation), FDA 21 CFRs, FDA 21 CFR 58, Digitalization, Toolchain/ALM/PLM coaching, process documentation, 93/42/EEC, 2007/47/EC, 2016/MDR (Medical Device Regulation), 510k submission, EN ISO 13485(Quality Management), EN ISO 14971 (Risk Management), EN 62304 (Software Lifecycle), Usability (EN 62366 & EN 60601-1-6), LIMS, FDA 21 CFR part 820. Other: DICOM, LOINC, HL7, FDA 21 CFR 803, FDA 21 CFR 806, MES, ISO/IEC 15026-2, ISO 9001, ISO 9003, GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GCLP/ GDP, EN 60601, IEC 12207, IEC 61508, ISO 61010, GAMP-CSV.
  • REQUIREMENTS ENGINEERING: Project experience in Requirements elicitation, analysis (project, negotiation, specification and modeling (e.g. SysML/UML) and management. Also Template creation, DXL scripting, etc. Variant Management for Requirements Engineering.
  • R&D, MODELING, SIMULATION, SYS&SW&HW DESIGN/ARCHITECTURE and Programming Techniques: Machine Learning/ Algorithmics/ Data Science/ Artificial Intelligence/ Big Data/ Neural Networks/ Deep Learning/ HMI development (Human Machine Interface) and Usability/ UI-UX/ User Interface/ User Experience/ IxDF/ Virtual Reality (VR) ? Augmented Reality (AR), SCRUM, Agile, V-Model, SysML, UML Modeling, OOA, OOD, OOP (Object Oriented Architecture, Design & Programming), Databases, AUTOSAR 4, Model-driven Development, Automatic Code Generation, Architecture & Design Patterns, Reverse Engineering.
  • QUALITY MANAGEMENT/ PROCESS: ISO 13485, Audits, Quality Management, Risk Management, GxP, GMP, GCP, GLP, GAMP 5, CSV, FMEA issuing and moderation as well as experience as Quality System and Software Engineer in the MedTech branch (DHF, DMR & DHR: development and remediation activities, and CAPA). Supplier Quality, Supplier Management, Reporting. Experience also as project manager for process improvement and assessment preparation, in an international multi-site development scenario. V-Model, SCRUM and Extreme Programming/Agile.
  • RISK MANAGEMENT & FUNCTIONAL SAFETY & Critical System Design & Development in the Medical Technologies, Pharma and Automotive Branches: Experience as Risk/ Functional Safety Manager, Functional Safety Engineer, Functional Safety Project Leader and Functional Safety SW implementation Team Leader. DIA (Development Interface Agreement), Risk and Hazard Analysis, Functional Safety Plan, Technical Safety Concept Specification (Reqs & Arch), FuSa HSI, FMEA, FTA, FMEDA, FuSa V&V (Testing), etc. ISO 14971, ISO 26262 and IEC 61508.
  • PROJECT MANAGEMENT/ TEAM LEADERSHIP: Project experience in Planning and Tracking, Scrum, Action Point List generation and tracking, meeting and workshop organization and chairing, preparation of slides for presentations, presentation skills, soft skills, cost calculation, budgeting, external resource acquisition, interviewing, commissioning.
  • Experience in BUSINESS MANAGEMENT, Marketing, International Relations, Client & Partner Acquisition & Care, Presentation & People Skills, Purchasing, Tax Systems and Contract Negotiation.
  • QUALITY ASSURANCE & TESTING: CSV (Computer System Validation), Testing Plan, Testing Management, Unit Testing, HIL, SIL, Unit Testing, Endurance/Long-term Testing, Automated & Managed Testing. Experience in Regulated (V-Model, Water-Fall), Agile and mix development environments. Understanding of the importance of client-facing roles, excellent customer service and communication skills. Good team member understanding of wrap-around development and testing processes. Solid understanding of test case design implementation and reporting, Regression testing and automation, Solid analytical approach, Good understanding of the place of creativity in the testing and mitigation process. Experience in Code Reviews and Static Rule Checking. Knowledgeable about different testing, development and defect tracking tools.
  • HARDWARE DEVELOPMENT & TESTING: PCB Schematics and layout (plus component footprints), EMC/EMV, FPGA development, laboratory testing experience.
  • MICROPROCESSORS: different Texas Instruments SoCs & DSPs, NVidia SOCs and GPUs, ALTERA SOCs, XILINX SOCs, Mobileye EyeQ, Infineon TriCore, TI Jacinto, TI OMAP 5, ARM7, ARM9, ARM11, ARM Cortex A15, ARM Cortex M4, Infineon Aurix, Freescale ColdFire, Renesas SH-4, Xilinx Microblaze.
  • EMBEDDED OPERATING SYSTEMS: RTOS and non-RTOS. OSEK, QNX, Embedded Linux, Express Logic ThreadX, MS WinCE, Texas Instruments DSP BIOS, Freescale MQX? Also experience with very low resources systems with no embedded operating system.
  • Areas of SPECIALIZATION in the SYSTEMS DEVELOPMENT: MedTech Devices, Pharma and Biotech (e.g. Pharma production facilities, minimal invasive chirurgical electro-mechanical devices -robots- for brain/spine surgery, MRT device, X-ray device, electronic blood infusion pumps, in-vitro diagnostics, video-cameras for medical appliances, pharma and medical research electronic devices).

Tools
  • RISK MANAGEMENT, FUNCTIONAL SAFETY and QUALITY MANAGEMENT: GessNet TurboAC, KPIT Medini Analyze, APIS IQ-SW, Plato FMEA, Method Park STAGES, LINT, Coverity, QAC, Polyspace, Klocwork, etc
  • REQUERIMENTS ENGINEERING: IBM DOORS (+ DXL), Polarion, MKS/PTC, HP Quality Center, Borland Caliber, Orcanos QPack, Banana Scrum, HOOD DESIRe, Pure::variants and Big Lever Gears for Variant Management in Requirements Engineering.
  • Process Definition, Modeling, Simulation, Product & Application Lifecycle Mgmt (PLM/ ALM), Integration, VERSION Control, CHANGE, CONFIGURATION, VARIANT Mgmt Tools, ReqEng, Testing, SW&HW ARCHITECTURE & DESIGN: BPMN (Business Process Model & Notation) & ADONIS BPM & ADOIT Suite, BPM/PBMN & ADONIS SysML & UML (IBM Rational Rhapsody, SparxSystems Enterprise Architect, MID Innovator, IBM Rational Rose, Microsoft VISIO and StarUML), Polarion, MKS / PTC Integrity, Perforce P4V, Telelogic-IBM ALM toolchain, Atlassian tools (JIRA, etc), Subversion and CVS, Serena Team Track & PVCS, pure systems pure::variants, BigLever Gears, GIT, MAVEN, Jenkins, IBM DOORS (+ DXL), HP Quality Center, Borland Caliber, Orcanos QPack
  • TEAM LEADING, PROJECT MANAGEMENT & OFFICE APPS: MS Office (Word, PowerPoint, Excel, Access, Visio), MS Project, Microsoft Team Foundation Server (MS TFS), Actano RPLAN e3, ERPs and Warehouse Mgmt (SAP, GUS, etc), Mindjet MindManager
  • PHARMA/ Biotech/ Medical/ LAB tools : Minitab, STARLIMS & LabWare LIMS & ELN, MES (for MedTech/Pharma/BioLabs)
  • SOFTWARE Development Environments, Programming Languages & Integration TOOLS: C/C++, Python & R, PyTorch, TensorFlow, Scikit-Learn, C#, VBScript, Java, LabView, MATLAB, Simulink, Delphi, SQL, PHP, Anaconda, Zeppelin & Jupyter Notebooks, Gitlab CI/CD, DVC (Data Version Control), Kubernetes, Docker, HADOOP, Amazon AWS, Value Cloud, Celery, ONNX AI, DJANGO, React ? JavaScript, REST APIs, GitOps, Argo CD, JIRA, Confluence, MS Team Foundation Server, Google Cloud, embedded C/C++, GitHub, MAVEN, Jenkins, Eclipse, Xilinx SDK, MS Visual Studio, Tableau, Freescale CodeWarrior, TI Code Composer Studio, IAR Embedded Workbench, Looker, ARM RealView Dev Suite, Qt, Tcl/Tk, D?Oxygen, Open GL (ES) API, NVidia GPUs, Adobe Flash Lite, etc.
  • QA/Testing: HP/MicroFocus Quality Center, GIT, Polarion/ Siemens Teamcenter (ALM ?PLM), Polarion TestRun, HP UFT, IBM Rational Functional Tester/ Rational Test Workbench/ Performance Tester, Parasoft Load Test, UserTesting, qTest Manager by QASymphony, Mockserver, Betamax, Borland Silk Perfomer, Automation Anywhere Testing Anywhere, TestPlant eggPlant, JUnit, MATALB, Simulink, Labview, JIRA, Mantis, Bugzilla, REDMINE, MISRA Rules QAC Checker, LINT, Klocwork, Coverity, PerlUnit, Test::Unit, Python, UnitTest++, QtTest, CppUtest, JUnit, TUX UTest, Tessy, IBM Rational Test Real Time (RTRT), Vector/CAN Tools (CANopen, CANoe, CANape & CANKing), etc.
  • HARDWARE DEVELOPMENT TOOLS & LANGUAGES: ALTIUM, ORCAD & EAGLE (schematics, footprints & layouts), Hyperlynx (EMC/EMV), Modelsim, VHDL, Verilog, SystemC (FPGAs)/ Oscilloscope & Logic Analyzer
  • MODELING & SIMULATION: MATLAB, Simulink, LabView, Ptolemy, Mentor Graphics ModelSim, Autodesk 3ds Max (3D Studio MAX), etc.

Programmiersprachen

Assembler
C
C#
C++
Java
MS Access Query
PHP
VBA

Branchen

Branchen

  • Medical Technologies
  • Life Sciences
  • Medical Devices
  • Biotech
  • Pharma
  • Technology applied Research on Life Sciences
  • Bioinformatics
  • Automotive

Einsatzorte

Einsatzorte

Deutschland, Österreich, Schweiz

Weltweit ansetzbar. Aber am besten wäre gleich in Valencia oder in Frankfurt, oder in der Nähe. Oder in Osteuropa Oder USA.

möglich

Projekte

Projekte

2023: ARTIFICIAL INTELLIGENCE, MACHINE LEARNING & DATA SCIENCE

Role: ARTIFICIAL INTELLIGENCE, MACHINE LEARNING & DATA SCIENCE ENGINEER / CONSULTANT / COACH / ADVISOR
Location: Germany & Remote
Customer: Start-Up

Tasks
  • Machine Learning/ Algorithmics/ Data Science/ Artificial Intelligence/ Big Data/ Neural Networks/ Deep Learning/ Software Architecture & Design/ Framework Concept & Development/ DevOps/ Programming/ Requirements Engineering-Management

Skills:
Python & R/ Anaconda/ PyTorch/ TensorFlow/ Scikit-Learn/ Zeppelin & Jupyter Notebooks/ ONNX AI/ Gitlab CI/CD/ DVC (Data Version Control)/ SQL/ SCRUM/ Agile/ Kubernetes/ Docker/ HADOOP/ Amazon AWS/ Value Cloud/ Celery/ DJANGO/ React ?JavaScript/ REST APIs/ GitOps/ Argo CD/ SysML/ UML/ BPMN/ JIRA/ Confluence


2022 - 2023: QUALITY MANAGEMENT/ COMPUTER SYSTEM VALIDATION/ GAMP 5 CSV/ SOPs & WIs/ PLANNING/ BPMN/ TEST MANAGEMENT

Role: SYSTEMS ENGINEER/ QUALITY MANAGEMENT/ COMPUTER SYSTEM VALIDATION/ GAMP 5 CSV/ SOPs & WIs/ PLANNING/ BPMN/ TEST MANAGEMENT
Location: Germany & Remote
Customer: BioNTech SE (PHARMA)

Tasks
  • Pharmaceutical Development & Production/ Digitalization of Paper-Based Pharmaceutical Manufacturing Process/ IQ (Installation Qualification)/ OQ (Operational Qualification)/ PQ (Performance Qualification)/ Databases/ GAMP5 CSV (Computer System Validation)/ SAP Cutover Planning and Execution/ Documentation Approvals/ Regulatory Affairs/ Write & Review SOPs (Standard Operating Procedures) & WIs (Working Instructions)/ SCM - Supply Chain Management Testing/ Test Management/ Quality Control/ Quality Management/ Clinical Trials/ SAP Introduction in the company/ Multi-site/ SW
  • ERP Tool Change Cutover Planning and Execution / SW Tool Deployment (SAP ERP in Supply Chain Mgmt) / FMEAs / BPMN 2.0 (Business Process Model and Notation) / BPM (Business Process Management) / ADONIS BPM Suite / Risk Management / Ris Assessments / FMEAs / FTAs / HAZOP / Corona Virus Vaccine / individualized Neoantigen/mRNA/cancer Specific Immunotherapy (iNeST) / Monoclonal Antibody Therapies (Cancer, etc)
  • Pharma Product / Pharmaceutical Production / IFUs (Instructions for Use) & O&M (Operation & Maintenance Manuals) / Systems Engineering / Documentation / Training / DMSs SOP-Guard & SOP-Form/ Software / Audit Trials / Changes / Databases / SQL / CAPAs / V-Model & SCRUM

Skills:
MS Office/ Adonis BPM/ GUS-OS ERP/ SAP ERP/ SOP-Guard/Alpega TMS/ MS Navision/ WinSped/ MS Teams ? Sharepoint/ LabWare LIMS & ELN/ MES


2022: RISK & QUALITY MANAGEMENT

Role: RISK MANAGER/ QUALITY MANAGEMENT/ FMEA MODERATION & ISSUANCE/ TEAM LEADING/ COORDINATION/ SYSTEMS ENGINEERING
Location: Germany & Remote

Tasks
  • RISK & QUALITY MANAGEMENT, Artificial Intelligence, Machine Vision & Sensor R&D
  • APIS IQ-RM Pro / DOORS / JIRA/ Medini Analyze / PTC-MKS Integrity/ Enterprise Architect
  • FMEA Issuance and Moderation (SYS/SW/HW/MD)/ Team Leading/ Coordination/ Systems Engineering/ Risk Management/ Requirements Engineering / Quality Management/ Documentation/ Coaching-Training/ Safety Related Hardware, Mechanical Design, Software and System Level FMEAs / FTAs / Safety Analysis / C-C++ / VB.NET


2020 - 2021: various projects

Role: TEAM LEAD/ REGULATORY AFFAIRS/ SYSTEMS ENGINEERING (+SW+HW+MD)/ RISK MANAGEMENT/ QUALITY MANAGEMENT/ REQUIREMENTS MANAGEMENT/ ALM- PLM CONSULTANT
Location: Ireland & Remote
Customer: MALLINCKRODT Pharmaceuticals (PHARMA & MedTech & Combination Products)

Tasks
  • 2 projects: Nitric Oxide pulmonary Delivery System (China registration) & Extracorporeal blood Photochemotherapy (ECP)/ Photopheresis System
  • Documentation Review and Approval, FDA & China & EU Submissions, PMAs/ IDEs/ 510Ks, Systems Engineering, Regulatory Affairs, Risk Management, Quality Management Quality Management, Documentation, Audits, Cross functional interfacing (Medical, Clinical, V&V, company management, Usability, RA, Legal, Marketing, Purchasing, Engineering, Quality, Risk Mgmt), stakeholder management, ALM/PLM Consultancy & Planning & Implementation, Systems Engineering, Requirements Engineering/Management, System Architecture, Software, Risk Management, Quality Management, Documentation, Reviews. DMS, V-Model, Microsoft Project, Enterprise Architect/EA/SysML/UML, JAMA ReqEng, listing of international standards, resource planning, budgeting, regulations and guidelines applicable to the project (including the conversion of clauses into design input requirements), gap analysis.
  • Phases: Planning, Development, Qualification & Post-Martket

Skills
ISO 13485:2016, 21 CFR/FDA, ISO 9001, MDD/IVD, MDR/IVDR, ISO 14971, EN 62304, EN 62366, CSV, GxP, GMP, GCP, GLP, GAMP, MES, LIMS. V-Model, SCRUM, Agile, Python, JAVA, JavaScript


2020: Development and Clearance of a fully integrated Operating Theater for an Operating/ Surgery Hospital Room

Role: TEAM LEAD/ SYSTEMS ENGINEERING/ QUALITY MANAGEMENT/ RISK MANAGEMENT/ GAP ANALYSIS
Location: Germany & Remote
Customer: KARL STORZ SE & Co.KG (MedTech)

Tasks
Functions: ALM-PLM Consultancy & Planning & Implementation, Systems Engineering Leading/ Risk Management Engineering/ Regulatory Affairs Support/ DMS/ Clearance Support

Skills:
Databases, SQL, VB.NET, JAVA, Labview, C# & Testing tools, Linux OS, RTLinux OS, Siemens Polarion & Teamcenter ( ALM ? PLM ) / FDA & EU Submissions, OOD, OOP, Video Processing, Streaming, Network protocols, SaMD (Software as a medical device), IEC 60601, MDD/IVD, MDR/IVDR, ISO 14971, AAMI TIR32, AAMI TIR57, 21 CFR 820, ISO 13485, IEC 6230, SysML, V-Model, Scrum, Agile


2019 - 2020: MEDICAL DEVICES & PHARMA

Role: LEAD AUDITOR/ QUALITY MANAGER
Location: Switzerland, France, Hungary and UK + Germany & Remote
Customer: HAEMONETICS (PHARMA & MedTech & Combination Products)

Tasks
  • Blood Filtering Systems, Blood & Plasma Collection Systems & Blood Management Systems
  • SOFTWARE & HARDWARE/ Quality Management/ Several Audits as Lead Auditor/ 1st and 2nd party Audits of Medical Device/ Pharma/ Combination Products companies, Supplier Audits, Internal Audits, mock-up Audits (CE Marking, MDSAP, preparation for Notified Body Audits)

Skills
ISO 13485:2016, MDSAP, GMP, GCP, GLP, GAMP 5, SaMD (Software as a Medical Device), 21 CFR/FDA, ISO 9001, MDD/IVD, MDR/IVDR, ISO 14971, EN 62304, EN 62366


2017 - 2018: Development and Market Clearance (especially USA/FDA and EU) of different Insulin Infusion Pump Systems/ Auto-injectors & Pens/ SaMD (Software as a Medical Device)

Role: QUALITY MANAGEMER/ REGULATTORY AFFAIRS/ RISK MANAGER/ SAFETY ASSURANCE CASES LEAD
Customer: YPSOMED & ROCHE DIABES CARE (PHARMA & MedTech & Combination Products)
Loctation: Germany & Switzerland & Remote

Tasks
  • MEDICAL TECHNOLOGIES (Class 2 device) and PHARMA (Combination Products)
  • Function: Regulatory Affairs Support/ Clearance Support/ Post-market/ Clinical Evaluation/ Clinical Trials/ Risk Manager/ Risk Assessments/ Supplier Management/ Safety Assurance Cases/ Quality Engineer/ Requirements Engineer
  • Goals: Engineering Lead/ FDA & EU Submissions (PMAs/510Ks/IDEs/CE-Mark)/ Resource planning/ Introduction of Software tools in the company/ Coordination of external partners and internal teams/ Budgeting/ Risk Management/ ALM-PLM
  • Consultancy & Planning & Implementation/ CSV (Computer System Validation)/ DMS/ Perform Safety Assurance Cases (SACs) ? including Cyber-Security -, SIEMENS MES, SIEMENS Opcenter, DMS, Labware LIMS, Preliminary Hazard Lists and Analysis, Risk Analysis, FTAs and FMEAs; DHF, DMR & DHR; SACs: in the case of insulin pumps, based on ?Infusion Pumps Total Product Life Cycle, Guidance for Industry and FDA Staff? (December 2, 2014)
  • RIMS/ Additional norms/ guidances/ papers applied/used: Papers on cybersecurity, ISO 14971/ ISO 15026/ MDD, MDR/ AAMI TIR32/ AAMI TIR57/ 21 CFR 820/ ISO 13485/ LIMS Labware/ IEC 62304/ IEC 60601/ WiFi/ Audits
  • Listing of international standards, regulations and guidelines applicable to the project, conversion of clauses into design input requirements (including assessment), gap analysis
  • Additional Tasks: CAPAs, interaction with the development and Regulatory Affairs teams; introduction of an appropriate SW tool for SAC performance; support of the introduction of the SAC work product and process into the company lifecycle; Cyber-Security; compilation of the Risk Management File (RMF)

Skills:
Java, JavaScript, Python, Angular & Testing tools/ V-Model, Agile, Scrum, UML, SysML/ LabWare LIMS & ELN, MES SAP, Siemens Polarion & Teamcenter (ALM ? PLM), Google Cloud/ Databases/ SQL, Polarion, DOORS, Turbo-AC, SaMD (Software as a medical device), GLP, GxP, Papers on cybersecurity, transition MDD/IVD to MDR/IVDR, GAMP5, Computer System Validation (CSV)


2016 - 2017: Submission & Audit & Development & DHF (Design History File) Remediation

Role: SYSTEMS ENGINEER/ QUALITY MANAGEMENT/ GAP ANALYSIS/ REGULATORY AFFAIRS/ COORDINATION/ TESTING
Customer: ZIMMER BIOMET (MedTech)

Tasks
minimal-invasive surgery robot (electro-mechanical device) - innovative highprecision brain & spine SURGERY
  • MEDICAL TECHNOLOGIES (Class 2b device)
  • SaMD (Software as a medical device), FDA 510k submission, 93/42/EEC, FDA & EU
  • Submissions, transition MDD/IVD to MDR/IVDR, 2007/47/EC, GAMP5, Java, JUNit, Labview, SAP, C#, Matlab Simulink, C++,Perforce, GLP, GxP, CSV (Computer System Validation), 93/42/EEC, 2007/47/EC, 2016/MDR (Medical Device Regulation), Regulatory Affairs/ Project Management/ DMS/ Clearance Support/ Systems Engineering/ Risk Management/ RIMs/ Quality Engineering/ Testing/ Post-market/ Clinical Evaluation/ Clinical Trials/ EN

Skills
ISO 13485(Quality Management), EN ISO 14971 (Risk Management), EN 62304 (Software Lifecycle), Usability (EN 62366 & EN 60601-1-6), FDA 21 CFR parts 820, 803 and 806


2014 - 2016: SAFETY CRITICAL SYSTEMS

Role: PROJECT MANAGER/ SYSTEMS LEAD/ RISK MANAGER/ FUNCTIONAL SAFETY MANAGERENGINEER/ TEAM LEAD
Location: GERMANY & Remote

Tasks
  • Audits, Presentations, coaching of development; checklists, templates and process definition
  • FMEA (and FMEDA) Issuing&Moderation, Java, Javascript, Labview, C#, Matlab Simulink, C++
  • Depending on the project, responsible, author, coordinator, reviewer and/or co-authour of different work products or responsible for the whole FuSa
  • Lifecycle: Hazard%Risk Analysis, Safety Concepts, FuSa effort estimation, customer contact, Functional Safety Plan, Impact Analysis, FMEA, FMEDA, FuSa Test Specs, Safety Case, FuSa Assessments, etc.

Skills:
Medini Analyze, APIS IQ, PTC Integrity and ReqEng, Subversion, MS Project, IBM DOORS, Enterprise Architect, MS Visio, Power Point, Excel


2013 - 2014: Audits/ DHF Remediation activities / Gap Analysis, Gap Assessment and Gap Closing

Role: SYSTEMS ENGINEER/ REGULATORY AFFAIRS/ QUALITY MANAGEMENT/ AUDITS/ SYSTEM ARCHITECTURE/ REQUIREMENTS ENGINEERING
Customer: B. BRAUN (PHARMA & MedTech & Combination Products)

Tasks
Audits/ DHF Remediation activities / Gap Analysis, Gap Assessment and Gap Closing
  • Planning and Execution / FDA-clearance (PMAs/510Ks) and improvement of existing Infusion Pump Systems
  • Function: Requirements Engineering/ Regulatory Affairs Support / Clearance Support/ Postmarket / Clinical Evaluation / Clinical Trials / System & Sw Senior Quality & Design Engineer/ Requirements Management/ V-Model / Agile / SCRUM / SysML

Skills:
DMS, Polarion, Supplier Management , RIMS, 21 CFR 820/ ISO 13485/ ISO 14971/ IEC 62304/ IEC 60601/ SIEMENS MES, SIEMENS Opcenter/ WiFi/ FDA clearance-approval process - FDA 21 CFR 803/ Cybersecurity/ CSV/ STARLIMS/ GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GLP/ GCLP/ GDP/ FDA 21 CFR 806/ Total Product Life Cycle, test case/ DHF, DMR & DHR/ Audits/ CAPAs/ Optics/ SQL, Java, JavaScript, GLP, GxP, CSV (Computer System Validation)


2012 - 2013: IVD Device - New Development of the to date highest throughput medical in-vitro diagnosis for different diseases (COVID, HIV, Hepatitis, etc.) based on PCR technology

Role: REQUIREMENTS ENGINEER-MANAGER/ QUALITY MANAGEMENT/ SCRUM MASTER/ TESTING/ RISK MANAGEMENT/ QUALITY CONTROL/ DEVELOPMENT ENGINEER
Customer: ROCHE Diagnostics (MedTech & PHARMA)

Skills:
Audits/ HL7/ LIMS/ C#/ Scrum/ V-Model/ Google Cloud/ Databases/ SQL/ ISO 13485/ ISO 14971/ IEC 62304/ IEC 60601/ EU & FDA clearance approval process/ FDA 21 CFR 820/ GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GLP/ GCLP/ GDP/ FDA 21 CFR 803 & 806


2011 - 2012: SW DEVELOPMENT FOR FUNCTIONAL SAFETY

Role: TECHNICAL PROJECT MANAGER (Engineering Product Leader - EPL), RISK MANAGER, FUNCIONAL SAFETY PROJECT LEAD and TEAM LEADER OF THE FUNCTIONAL SAFETY SW-DEVELOPMENT TEAM
Location: Southern Region, GERMANY. (/remote)

Tasks
  • MS Project, IBM DOORS, MS Visio, MS Power Point, MS Excel, Atlassian JIRA & Confluence, Enterprise Architect/ ISO 26262, Automotive SPICE, AUTOSAR 4, FlexRay, CAN, Python
  • Engineering Project Manager (composed of HW-Team, SW-Team, Mech-Team, Test and Validation Teams, ?), team of ca. 60 people. Multi-cultural and multi-location team (6 locations in different countries)
  • Audits, Functional Safety (ISO 26262) project leader (HW+SW) & Team Leader/ Functional Owner of the FuSi-SW-Development team (ca. 8 people)
  • Multi-location/ remote team (4 locations)

Skills:
C, C++, VxWorks OS, DSP, CppUTest


2011: QUALITY MANAGEMENT/ QUALITY ASSURANCE TEAM LEAD/ ASSESSMENT PREPARATION

Role: Multisite (& multi-country) Team Leading
Location: GERMANY & Remote

Tasks
  • Audits, MS Project, MS Power Point, IBM/Telelogic Rational DOORS
  • Multisite (& multi-country) Team Leading
  • Goal of the Project: Process Improvement of a multi-site development as preparation for an Assessment
  • Disciplines: Requirements Management, Version Control Management, Change Management, Software Development and Testing
  • Typical Tasks: organization of meetings and workshops (with engineers, quality managers and discipline managers), chair meetings, prepare presentation slides, hold presentations, write down minutes, hold presentations and trainings, slide preparation,business trips to sites in other countries, project planning, process analysis, coordination, arrive to agreements among the different teams, commissioning, Action Item List creation and management / C, C++, VxWorks OS, Microcontrollers


2010 - 2011: SAFETY CRITICAL SYSTEMS

Role: SOFTWARE DEVELOPER/ TESTER/ REQUIREMENTS ENGINEERING/ SW DESIGN & ARCHITECTURE
Location: Northern Region, GERMANY & Remote

Skills:
Video-processing, DSP, OpenGL, Adobe Video libraries, C, C++, Qt, Microsoft Windows RT OS, Perl , PerlUnit, Test::Unit, Python, UnitTest++, QtTest


2010 - 2011: Precision electronic system for liquid-powder mixing

Role: REQUIREMENTS MANAGER -HP QUALITY CENTER- AND SYSTEMS & SW ARCHITECT
Customer: METTLER-TOLEDO (MedTech), SWITZERLAND

Tasks
Precision electronic system for liquid-powder mixing to be used in the Pharma
  • Industry and Medical Research/ Cybersecurity/ CSV/ LIMS/ DMS/ GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GLP/ GCLP/ GDP/ LabWare LIMS/ Test Case Derivation, Development, Execution and Reporting/ SIEMENS MES, SIEMENS Opcenter/ V-Model/ Agile/ SCRUM
  • PHARMA/ MEDICAL TECHNOLOGIES/ WiFi / PRECISION MEASUREMENT ELECTRONICS
  • Function: Audits/ Requirements Engineering/ Regulatoy Affairs Support/ Clearance Support/ Post-market/ Clinical Evaluation/ Clinical Trials/ System & Sw Senior Quality & Design Engineer/ Requirements Management


other projects on request

Aus- und Weiterbildung

Aus- und Weiterbildung

2002
Master?s Degree (5-years worldwide-accepted University program) in Telecommunications Engineering ? Specialties Electronics & Telecommunications, UPV Valencia, Spain

Certifications/ Trainings
  • MEDICAL TECHNOLOGIES, MEDICAL DEVICES, Biotech : AUDIT-GARANT (Advanced Professional Program for Medical Device Development and Clearance Process (Regulatory Affairs, Quality Mgmt, Technical Documentation and System Development: 47/EC, MDR, 510k, ISO 13485, ISO 14971, EN 62304, EN 62366, EN 60601-1-6, 21 CFR, HL7, DICOM, LOINC, GxP), Johner Institute
  • Different trainings on PHARMA & BioTech: GMP, GAMP5 Computer System Validation (CSV), User Requirements (URS) and Functional Specifications (FS) Definition, Risk Analysis&Management, Change Control, different DMSs (Document Management Systems), CAPAs and Action Management, ERPs and Supply Change Management and Warehouse Management Systems (SAP,GUS, etc)
  • Medical Devices LEAD AUDITOR Certification - bsi Group (Notified Body, British Standards Institution), 5 days, Frankfurt, Germany (ISO 19011:2018 / ISO 13485:2016)
  • MDSAP Auditor Training (Medical Device Single Audit Program) ? bsi Group (Notified Body, British Standards Institution), 2 days
  • INCOSE CSEP Systems Engineering Professional Certification Training
  • Certified Requirements Manager ? IREB
  • FMEA moderator Training (4 days) - KVP Institut
  • Certified Risk Manager (TüV Nord)
  • IVDR Trainings
  • MDR (Medical Device Regulation) Implementation for CE-Marking ? Training Course - bsi Group (Notified Body, British Standards Institution), 3 days, Frankfurt, Germany
  • Clinical Trials/ Clinical Studies of Medical Products. 2 days training, June 2018, Bonn/ FORUM Institut für Management
  • 3-day hands-on training about Safety Assurance Cases for Medical Devices - GessNet
  • Certified Auditor (ISO 13485:2016) ? Johner Institut, Germany
  • LIMS trainings
  • BPMN (Business Process Model & Notation) & ADONIS BPM & ADOIT Suite Training, 2 days
  • Several days of individual Training&Coaching in Project Management, Presentation, Interaction, Time Management and Rhetoric skills, techniques and tools
  • isQI CPMS (Certified Professional for Medical Software) ? currently Exam preparation
  • iSQI ISTQB Certified Tester, currently Exam Preparation

Position

Position

  • SYSTEMS ENGINEER/ REQUIREMENTS MANAGER (Customer & System & HW & SW Reqs)/ System & HW & Software ARCHITECT/ MedTech, Pharma and Biotech SENIOR ENGINEER
  • TEAM LEAD/ PROJECT MANAGER/ PM/ Scrum Master/ Scrum Product Owner
  • AI (Artificial Intelligence)/ ML (Machine Learning)/ Data Science/ Algorithm Engineer
  • RISK MANAGER (MedTech, Pharma, Biotech and Combination Products)/ Functional Safety Engineer & Manager
  • QUALITY MANAGER/ LEAD AUDITOR/ REGULATORY AFFAIRS/ Technical Documentation
  • FMEA (also FMEDA) Issuer/ Moderator
  • Software Development/ Programming
  • TESTING/ Quality Assurance/ Validation/ CSV ? Computer System Validation / Verification/ Test Management
  • HW Development/ Mechanical Design

Kompetenzen

Kompetenzen

Top-Skills

Requirements Engineering Teamleading Risikomanagement Künstliche Intelligenz Data Scientist FMEA Algorithmics Projektmanagement/Projektleitung Systems Engineering SystemArchitektur CVS DIN 13485 ISO 14971 IEC 62304 IEC 62366 Machine Learning

Produkte / Standards / Erfahrungen / Methoden

Actano RPLAN e3
AUTOSAR 4
C++ Standard Template Library (STL)
CAN
Embedded OpenGL
for C++
Ethernet
FireWire
FlexRay
MATLAB
for C
Microsoft Team Foundation Server (MS TFS)
Mindjet MindManager
MOST
MS Office
Word, PowerPoint, Excel, Access, Visio
MS Project
OpenOffice
PERL
for C
SAP
SysML
UML

Professional Experience

  • More than 10 projects in the fields of MEDICAL TECHNOLOGIES, MEDICAL DEVICES, BIOTECH, PHARMA and combination products. More than 20 years of professional experience in international teams, mainly in Germany and Switzerland, but also in Ireland, the USA, the UK, Spain, France, Italy, Romania, Austria and Hungary, as well as with various teams in Sweden, Mexico, Egypt, Israel, Australia and Asia (China, South Korea, India, Philippines and Japan).
  • Other end customers and employers in other business areas: CERN (European Organisation for Nuclear Research)
  • Additional Know-How in Pharma, BioTech, Biomedicine & Biology ? Cancer, Aging, Longevity, Omics ?Genomics, Epigenomics, Proteomics, Transcriptomics, Metabolomics-, Lab-grown organs, etc (Research, Services, Products, Networking, etc)
  • Several Audits: supplier Audits, internal Audits, mock-up Audits (ISO 13485, MDSAP, GCP, GMP, GAMP 5, GLP, GxP, FDA 21 CFRs, FDA 21 CFR 58, ISO 9001, ISO 14971, EN 62304, EN 62366, EN 60601, EU/ MDD/ MDR/ IVDD/ IVDR, USA/FDA, Canada/HC, Australia/TGA, Brasil/ANVISA, Japan/MHLW, etc)

SKILLS & TECHNOLOGIES
  • Applied and theoretical knowledge of MEDICAL TECHNOLOGIES/ PHARMA/ BioTech Specifications and Laws/Regulations: Design, Quality, Regulatory Affairs, GxP, GMP, GCP, GLP, GAMP 5, CSV (Computer System Validation), FDA 21 CFRs, FDA 21 CFR 58, Digitalization, Toolchain/ALM/PLM coaching, process documentation, 93/42/EEC, 2007/47/EC, 2016/MDR (Medical Device Regulation), 510k submission, EN ISO 13485(Quality Management), EN ISO 14971 (Risk Management), EN 62304 (Software Lifecycle), Usability (EN 62366 & EN 60601-1-6), LIMS, FDA 21 CFR part 820. Other: DICOM, LOINC, HL7, FDA 21 CFR 803, FDA 21 CFR 806, MES, ISO/IEC 15026-2, ISO 9001, ISO 9003, GxP/ GEP/ GMP/ GAMP/ GCP/ GCP/ GCLP/ GDP, EN 60601, IEC 12207, IEC 61508, ISO 61010, GAMP-CSV.
  • REQUIREMENTS ENGINEERING: Project experience in Requirements elicitation, analysis (project, negotiation, specification and modeling (e.g. SysML/UML) and management. Also Template creation, DXL scripting, etc. Variant Management for Requirements Engineering.
  • R&D, MODELING, SIMULATION, SYS&SW&HW DESIGN/ARCHITECTURE and Programming Techniques: Machine Learning/ Algorithmics/ Data Science/ Artificial Intelligence/ Big Data/ Neural Networks/ Deep Learning/ HMI development (Human Machine Interface) and Usability/ UI-UX/ User Interface/ User Experience/ IxDF/ Virtual Reality (VR) ? Augmented Reality (AR), SCRUM, Agile, V-Model, SysML, UML Modeling, OOA, OOD, OOP (Object Oriented Architecture, Design & Programming), Databases, AUTOSAR 4, Model-driven Development, Automatic Code Generation, Architecture & Design Patterns, Reverse Engineering.
  • QUALITY MANAGEMENT/ PROCESS: ISO 13485, Audits, Quality Management, Risk Management, GxP, GMP, GCP, GLP, GAMP 5, CSV, FMEA issuing and moderation as well as experience as Quality System and Software Engineer in the MedTech branch (DHF, DMR & DHR: development and remediation activities, and CAPA). Supplier Quality, Supplier Management, Reporting. Experience also as project manager for process improvement and assessment preparation, in an international multi-site development scenario. V-Model, SCRUM and Extreme Programming/Agile.
  • RISK MANAGEMENT & FUNCTIONAL SAFETY & Critical System Design & Development in the Medical Technologies, Pharma and Automotive Branches: Experience as Risk/ Functional Safety Manager, Functional Safety Engineer, Functional Safety Project Leader and Functional Safety SW implementation Team Leader. DIA (Development Interface Agreement), Risk and Hazard Analysis, Functional Safety Plan, Technical Safety Concept Specification (Reqs & Arch), FuSa HSI, FMEA, FTA, FMEDA, FuSa V&V (Testing), etc. ISO 14971, ISO 26262 and IEC 61508.
  • PROJECT MANAGEMENT/ TEAM LEADERSHIP: Project experience in Planning and Tracking, Scrum, Action Point List generation and tracking, meeting and workshop organization and chairing, preparation of slides for presentations, presentation skills, soft skills, cost calculation, budgeting, external resource acquisition, interviewing, commissioning.
  • Experience in BUSINESS MANAGEMENT, Marketing, International Relations, Client & Partner Acquisition & Care, Presentation & People Skills, Purchasing, Tax Systems and Contract Negotiation.
  • QUALITY ASSURANCE & TESTING: CSV (Computer System Validation), Testing Plan, Testing Management, Unit Testing, HIL, SIL, Unit Testing, Endurance/Long-term Testing, Automated & Managed Testing. Experience in Regulated (V-Model, Water-Fall), Agile and mix development environments. Understanding of the importance of client-facing roles, excellent customer service and communication skills. Good team member understanding of wrap-around development and testing processes. Solid understanding of test case design implementation and reporting, Regression testing and automation, Solid analytical approach, Good understanding of the place of creativity in the testing and mitigation process. Experience in Code Reviews and Static Rule Checking. Knowledgeable about different testing, development and defect tracking tools.
  • HARDWARE DEVELOPMENT & TESTING: PCB Schematics and layout (plus component footprints), EMC/EMV, FPGA development, laboratory testing experience.
  • MICROPROCESSORS: different Texas Instruments SoCs & DSPs, NVidia SOCs and GPUs, ALTERA SOCs, XILINX SOCs, Mobileye EyeQ, Infineon TriCore, TI Jacinto, TI OMAP 5, ARM7, ARM9, ARM11, ARM Cortex A15, ARM Cortex M4, Infineon Aurix, Freescale ColdFire, Renesas SH-4, Xilinx Microblaze.
  • EMBEDDED OPERATING SYSTEMS: RTOS and non-RTOS. OSEK, QNX, Embedded Linux, Express Logic ThreadX, MS WinCE, Texas Instruments DSP BIOS, Freescale MQX? Also experience with very low resources systems with no embedded operating system.
  • Areas of SPECIALIZATION in the SYSTEMS DEVELOPMENT: MedTech Devices, Pharma and Biotech (e.g. Pharma production facilities, minimal invasive chirurgical electro-mechanical devices -robots- for brain/spine surgery, MRT device, X-ray device, electronic blood infusion pumps, in-vitro diagnostics, video-cameras for medical appliances, pharma and medical research electronic devices).

Tools
  • RISK MANAGEMENT, FUNCTIONAL SAFETY and QUALITY MANAGEMENT: GessNet TurboAC, KPIT Medini Analyze, APIS IQ-SW, Plato FMEA, Method Park STAGES, LINT, Coverity, QAC, Polyspace, Klocwork, etc
  • REQUERIMENTS ENGINEERING: IBM DOORS (+ DXL), Polarion, MKS/PTC, HP Quality Center, Borland Caliber, Orcanos QPack, Banana Scrum, HOOD DESIRe, Pure::variants and Big Lever Gears for Variant Management in Requirements Engineering.
  • Process Definition, Modeling, Simulation, Product & Application Lifecycle Mgmt (PLM/ ALM), Integration, VERSION Control, CHANGE, CONFIGURATION, VARIANT Mgmt Tools, ReqEng, Testing, SW&HW ARCHITECTURE & DESIGN: BPMN (Business Process Model & Notation) & ADONIS BPM & ADOIT Suite, BPM/PBMN & ADONIS SysML & UML (IBM Rational Rhapsody, SparxSystems Enterprise Architect, MID Innovator, IBM Rational Rose, Microsoft VISIO and StarUML), Polarion, MKS / PTC Integrity, Perforce P4V, Telelogic-IBM ALM toolchain, Atlassian tools (JIRA, etc), Subversion and CVS, Serena Team Track & PVCS, pure systems pure::variants, BigLever Gears, GIT, MAVEN, Jenkins, IBM DOORS (+ DXL), HP Quality Center, Borland Caliber, Orcanos QPack
  • TEAM LEADING, PROJECT MANAGEMENT & OFFICE APPS: MS Office (Word, PowerPoint, Excel, Access, Visio), MS Project, Microsoft Team Foundation Server (MS TFS), Actano RPLAN e3, ERPs and Warehouse Mgmt (SAP, GUS, etc), Mindjet MindManager
  • PHARMA/ Biotech/ Medical/ LAB tools : Minitab, STARLIMS & LabWare LIMS & ELN, MES (for MedTech/Pharma/BioLabs)
  • SOFTWARE Development Environments, Programming Languages & Integration TOOLS: C/C++, Python & R, PyTorch, TensorFlow, Scikit-Learn, C#, VBScript, Java, LabView, MATLAB, Simulink, Delphi, SQL, PHP, Anaconda, Zeppelin & Jupyter Notebooks, Gitlab CI/CD, DVC (Data Version Control), Kubernetes, Docker, HADOOP, Amazon AWS, Value Cloud, Celery, ONNX AI, DJANGO, React ? JavaScript, REST APIs, GitOps, Argo CD, JIRA, Confluence, MS Team Foundation Server, Google Cloud, embedded C/C++, GitHub, MAVEN, Jenkins, Eclipse, Xilinx SDK, MS Visual Studio, Tableau, Freescale CodeWarrior, TI Code Composer Studio, IAR Embedded Workbench, Looker, ARM RealView Dev Suite, Qt, Tcl/Tk, D?Oxygen, Open GL (ES) API, NVidia GPUs, Adobe Flash Lite, etc.
  • QA/Testing: HP/MicroFocus Quality Center, GIT, Polarion/ Siemens Teamcenter (ALM ?PLM), Polarion TestRun, HP UFT, IBM Rational Functional Tester/ Rational Test Workbench/ Performance Tester, Parasoft Load Test, UserTesting, qTest Manager by QASymphony, Mockserver, Betamax, Borland Silk Perfomer, Automation Anywhere Testing Anywhere, TestPlant eggPlant, JUnit, MATALB, Simulink, Labview, JIRA, Mantis, Bugzilla, REDMINE, MISRA Rules QAC Checker, LINT, Klocwork, Coverity, PerlUnit, Test::Unit, Python, UnitTest++, QtTest, CppUtest, JUnit, TUX UTest, Tessy, IBM Rational Test Real Time (RTRT), Vector/CAN Tools (CANopen, CANoe, CANape & CANKing), etc.
  • HARDWARE DEVELOPMENT TOOLS & LANGUAGES: ALTIUM, ORCAD & EAGLE (schematics, footprints & layouts), Hyperlynx (EMC/EMV), Modelsim, VHDL, Verilog, SystemC (FPGAs)/ Oscilloscope & Logic Analyzer
  • MODELING & SIMULATION: MATLAB, Simulink, LabView, Ptolemy, Mentor Graphics ModelSim, Autodesk 3ds Max (3D Studio MAX), etc.

Programmiersprachen

Assembler
C
C#
C++
Java
MS Access Query
PHP
VBA

Branchen

Branchen

  • Medical Technologies
  • Life Sciences
  • Medical Devices
  • Biotech
  • Pharma
  • Technology applied Research on Life Sciences
  • Bioinformatics
  • Automotive

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