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Lächelnde Mitarbeiterin im Gespräch mit Kollegin im Büro
Lächelnde Mitarbeiterin im Gespräch mit Kollegin im Büro
ID: 115674

Technical Manager and Process Expert

  • MedTech
  • Asap
  • Interim Quality Manager, ISO 9001, OEE Improvement
  • K-Recruiting GmbH
Ansprechpartner:

Julius Strack

+49 89 1890998-21

julius.strack@k-recruiting.com

Overview

Availability
Asap; 5 days/week; onsite & remote
Qualification
Diploma in Engineering (FH), Certified FMEA Moderator, Six Sigma Green Belt, DGQ/EOQ Lead Auditor ISO 19011, TÜV Energy Management Officer
Language Skills
German (native), English (business fluent)
Relevant Expertise
Interim Quality Manager, ISO 9001, 13485, IATF 16949, FMEA, Root-Cause Analysis, CAPA Methods, Lean Six Sigma, OEE Improvement, Auditing, Leadership Development

Key-Facts

  • In several production environments (MedTech, Automotive), they reduced scrap rates by more than 30% through structured FMEA analyses, CAPA processes, and data-driven process control

  • As FMEA Moderator and DGQ/EOQ Lead Auditor, they combine analytical thinking with pragmatic implementation, establishe sustainable risk assessment, train teams in FMEA logic and ensure measurable process stability

  • They combine strategic leadership experience with strong operational execution when restructureing quality departments, stabilizeing processes and successfully manageing handovers to successors

  • With over 17 years of auditing experience according to ISO 9001, 13485, 14001, and 45001, they stabilize management systems quickly and safely guide them through external certifications

Extract from Previous Activities

Independent Consultant / Own Company

Process Optimization & Quality Manager

  • A highly qualified professional with a degree in engineering and certifications in FMEA moderation, Six Sigma Green Belt, and lead auditing

  • Possesses extensive experience in quality management, process optimization, and risk assessment in various industries including MedTech and Automotive

  • Known for reducing scrap rates significantly through structured analyses and process improvements

  • Combines strategic leadership with operational execution, having restructured quality departments and stabilized management systems

  • Over 17 years of auditing experience

MedTech Company

Interim Head of Quality & Process Optimization

  • Full responsibility for Quality Management, Quality Assurance, and Laboratory Operations

  • Conducted FMEA-based analysis and reorganization of quality processes to identify systemic weaknesses

  • Introduced structured CAPA management (8D, SCAR, Root Cause Matrix) for sustainable defect elimination

  • Significantly reduced scrap and complaint rates (>30%) through process monitoring and staff training

  • Built and led a cross-functional root-cause analysis team (Production, Engineering, R&D)

  • Implemented digital deviation and change-management tools integrated with audit and KPI systems

  • Conducted internal audits and prepared external certifications (ISO 13485, MDSAP)

  • Provided coaching and knowledge transfer to ensure a stable transition to the successor

MedTech Company

Interim Technical & Process Manager

  • Restructured the technical department

  • Established a Continuous Improvement Process (CIP) to reduce technical downtime causes

  • Implemented OEE monitoring and failure data analysis to identify key loss drivers

  • Conducted FMEA workshops with maintenance and production to prevent failures proactively

  • Optimized maintenance and logistics workflows, reduced technical failures by mor than 20%

  • Integrated Lean methods into daily management routines and shopfloor meetings

  • Coached the technical director during the transition phase

Engineering Service Provider

Technical Manager and Process Expert

  • Setup & Integration of SCC-FAZ / ISO 9001

  • Developed and implemented an HSE management system

  • Prepared for ISO 9001 certification including process design and approval

  • Defined process interfaces and documentation logic following ISO structure

  • Established an FMEA-based risk management process for operational activities

  • Trained management in internal auditing and root cause methodology, resulting in a structured, audit-ready management system as a foundation for certification

MedTech Company

Process Integration & Energy Manager

  • Further developed the Energy Management System (ISO 50001) and integrated it into the existing IMS

  • Defined new process interfaces and risk assessments in line with ISO 9001

  • Optimized audit cycles and KPI management for energy and quality

  • Trained management to incorporate new legal requirements, resulting in the full integration of energy management into the IMS structure – zero audit deviations

Cosmetics Company

Process Optimization & Leadership Coach

  • Introduced Value Stream Mapping and SMED to reduce setup times and minimize internal errors

  • Defined new performance metrics (FPY, Scrap Rate, MTBF, CAPA cycle time) for targeted process control

  • Built a Standard Work System and visual management to stabilize processes

  • Coached team and department leaders on root cause analysis and FMEA thinking

  • Revised audit and supplier management for preventive defect avoidance

  • Simplified documentation, checklists, and material inspection requirements (reduced administrative workload by >40%)

MedTech Company

Interim Head of Integrated Management System

  • Consolidated eight management systems into one integrated system (ISO 9001, 13485, 14001, 45001, 50001)

  • Harmonized processes and interfaces, defined clear audit structures

  • Introduced a Europe-wide FMEA framework for standardized risk analysis

  • Developed a Continuous Improvement Program focusing on OEE improvement and process stability

  • Created a KPI dashboard (audit findings, FMEA status, CAPA tracking)