k
killianrmz

Killian R

@killianrmz

IATF 16949 Auditor ShopFloor Quality Systems QMS Process Quality, CI Compliance

Mexique
Espagnol, Anglais
Certaines informations sont présentées en anglais.
À propos de moi
I am a Materials Engineer specializing in the administration, control, and auditing of Integrated Management Systems (HSEQ/IMS) in demanding manufacturing environments. My experience encompasses operational and document management under standards such as ISO 9001, IATF 16949, AS9100, and FSSC 22000. I have coordinated internal audits, corrective action closures, and product release documentation across the automotive, aerospace, and packaging sectors.... Plus d’infos

Compétences

k
killianrmz
Killian R
hors ligne • 
Temps de réponse moyen de 1 heure

Voir mes services

Gestion de projet
I will organize your document control system for iso 9001 iatf 16949
Gestion de projet
I will do an internal audit on your small business based on iso

Expérience professionnelle

Tuopu_USA

QMS Audits Shopfloor & Document Control Engineer

Tuopu USA • Temps plein

Aug 2026 - Present • 2 mos

Quality Assurance and Processes: Planning and execution of process (P5-P7), product, and layered process audits (LPA) in accordance with IATF 16949. Problem-solving and root cause analysis (8D / 5 Whys) for the closure of non-conformities. Monitoring of quality metrics (KPIs), control plans, PFMEA, and Core Tools (SPC/MSA) on the production floor. Management Systems, Document Control, and Training: Management of the QMS documentation lifecycle (issuance, review, bilingual version control, and obsolescence). Control of customer standards and external regulations applicable to the quality system. Management and tracking of the QMS training plan to ensure compliance during internal and external audits. Training of operational and administrative personnel on the proper use of documents and their lifecycle. Continuous Improvement (CI): Root cause analysis and problem-solving using 8D and 5 Whys methodologies for the timely closure of non-conformities. Coordination of Daily Quality Fast Response and tracking of corrective action closure.

Converforma

Integrated Systems Engineer Jr

Converforma • Temps plein

Mar 2026 - Aug 2026 • 5 mos

Integrated Management System (IMS) Administration: Coordination of document control and master lists (both physical and electronic) to ensure compliance with ISO 9001:2015 and FSSC 22000 standards, as well as SMETA (Sedex) ethical protocols, across multiple operational plants. · Internal Audits and Non-Conformity Closure: Execution of internal audits (ISO 9001/FSSC 22000) and evidence gathering to track and close corrective actions using the Root Cause Analysis (8D) methodology. · Regulatory Compliance and Change Management: Quarterly verification of the validity of applicable standards and participation in planning meetings for process and infrastructure changes to ensure IMS traceability. · Training and Organizational Culture: Delivery of EHS, Quality, and Food Safety induction programs for new operational and administrative staff; organization of quality and safety culture events. · Indicators/KPIs: Adherence to the internal audit plan, effectiveness of corrective actions, quality culture awareness (shared with food safety personnel), updating of international standards, and compliance with monthly document updates (additions, removals, and revisions).

SP_Manufacturas

Quality Assurance Engineer

SP Manufacturas • Temps plein

Oct 2025 - Feb 2026 • 4 mos

· Standardization and document control: Development and implementation of visual aids, work instructions, and shop-floor inspection plans, ensuring the continuous updating of the Quality Management System (QMS) master list. · Inspection and personnel management: Supervision and operational assignment of the quality inspection team, validating compliance with product release and process control standards. · Auditing and corrective actions: Execution of internal audits to identify and analyze QMS non-conformities, coordinating the implementation of corrective and preventive actions (CAPA) to eliminate root causes. · Training and metrics (KPIs): Development and monthly tracking of quality Key Performance Indicators (KPIs), delivering operational training to process owners to raise the level of regulatory compliance.