 Supplier control complains related with quality issues.  Define incoming inspections controls according to quality risk. First article inspection control from the new products under VDA standards. MPT Audits, APQP, PPAP validation  Transfer from programs to improve quality from suppliers. Mentoring in quality topics the purchasing team and internal training the ASQ Team. Technical reviews with supplier about actual design and possible solutions in order to reduce cost. Support purchasing department by improvement quality reducing claims, and cost reduction through improvement from supplier. MPT Audits, APQP, PPAP validation

 Development of supplier from friction material until the final production process.  Transfer from programs to improve quality from suppliers.  Transfer from improvements control from customer claims to suppliers, and verifications of the corrective and preventive actions.  First article inspection control from the new products.

 Evaluation from supplier and supply chain .  To perform supplier audits and to prove the corrective and preventive actions.  Generate and to agree specifications with suppliers as well as define the incoming inspections controls.  Claim control, and corrective improvement development action plan. Qualification material and process for different projects in optic, mechanical component and solar array.  Analyze problems in quality and look for one solution

The execution of the factory’s planning. The control and management of ISO9001 in the factory, and assisting with the management of ISO14000, FSC, PEFC, Health registry.The Control and reduction of stocks and warehouse.The Quality Control of raw materials and the final product, paper in reels and in bobbins for the printing paper and the tobacco industry.The management of the Quality Lab and the Research & Development Lab.To manage the internal and external quality audits, customer complaint, out of compliance, corrective and preventative actions.

Preparation and production of the reports including company authorized suppliers for Medical and Rehabilitation products.Execution, control and management of the manufacturing process in the factory. Development and realisation of new moulds, materials and products, design control, customer and supplier control. Preparation of budgets and technical documentation (drafts and others reports and files).The execution of the factory’s planning, control of stocks, maintenance, new productions process and communications with customers/suppliers.To help in the management of quality auditsTo search new customers/suppliers commercial and promotional tasks

Fellowship in the Newark University (Delaware-USA) Center for Composites Materials to investigate and develop a station to measure the permeability in compound resins materials. Design and manufacture composites materials parts with RTM (Resin transfer moulding) and VRTM (Vacuum resin transfer moulding) methods, improving their resistance, supervised by Doctor Suresh Advani

Production technical reports about medical products, production of information about qualifications of welder in all positions, and testing of materials wear and corrosion. Development and implantation in the enterprise quality standard regulations UNE-EN-ISO 9000 (considered equal to ASTM). Obtaining the certificate of Registered Enterprise in the IQ-net with the ER-1363/2/00 number by AENOR (Spanish Association of Normalization and Certification)Development and realisation of new process, reduction costs and improvements plansTo manage the internal and external quality audits customer complaint, out of compliance, corrective and preventative actions