For our Client – an international automotive company, we are looking for the best Candidate for the position of Responsibilities: Management of supplier panel in assigned commodity and segment, Participation is sourcing of new parts; Implementation of Technical Productivities (savings) and resourcing actions with suppliers as well as internal functions, Systematic activities for identifying Technical ...
Supplier Quality Assurance Opole NR REF.: 1089213 Dla naszego Klienta, międzynarodowej firmy z branży motoryzacyjnej, poszukujemy Kandydatów na stanowisko Supplier Quality Assurance.Do zadań na stanowisku Inżyniera jakości dostawców będzie należało m.in: utrzymywanie stałego kontaktu
improvement of the local Quality Management System Responsibility for process improvements initiatives REQUIREMENTS Master degree in pharmacy, chemistry or a similar natural science Multiple years' relevant work experience in the Quality department within
Supplier Quality Engineer Katowice NR REF.: 1086811 Dla naszego Klienta, międzynarodowej firmy z obszaru automatyki przemysłowej poszukujemy obecnie Kandydatów na Stanowisko Supplier Quality Engineer.Do zadań na tym stanowisku będzie należała bieżąca analiza sytuacji jakościowej
PDCA, CAPA) Cost Reduction projects with clients Implementations of new ideas and equipment Organize meeting with Quality Improvements Team Your qualifications We expect that you have at least a Bachelor's degree in Quality Management Lean SiX Sigma certification would be a plus 5 years of increasingly
quality issues with suppliers (with procurement and SQE) and other Xylem sites, and also status of the components approval for either new products or new suppliers. Supporting supplier transition phases with other departments, performing failure analysis field issues, addressing containment (firewall ...
you'll need to succeedA perfect candidate should have higher technical diploma and previous work experience in the area of quality or manufacturing of electronic or electromechanical automotive environment. We are looking for candidates with strong interpersonal skills and proactive approach. Very good
accordance with all necessary GxP, Quality regulations and standards Responsibility over maintaining the QMS Management Reviews Ensuring the implementation and enforcement of QMS for the affiliate and GxP suppliers. Ensuring the creation, maintenance and implementation Preparing and conducting Quality
REQUIREMENTS • BSc or MSc in Life Science related fields • +-3 years of experience in Quality Assurance in the medical device industry • Knowledge of the medical devices regularity and quality standards (GMP guidelines, ISO 13485, 21CFR820, European Directive 2004/23) • Expert in internal
securing and monitoring the quality policies. Supporting and advising at entering new and improved products into the market. Assure that they comply with applicable international regulations. - Implementing and monitoring internal and supplier audits, Independently and in teams. - You will Instruct ...
supplier audits, Independently and in teams • Coordination and follow up of extern audits • Initiating and monitoring the progress of corrective and preventive actions • Preparing, measuring and releasing of several documents • Quality control and releasing of produced products • Active supporting of the
Systems bezüglich der gesetzlcihen und Konzernvorgaben . Fokus auf: Issue Management (CAPA): Koordination, Dokumentation, Follow up und Monitoring aller anfallenden Vorfälle (Issues) - Supplier Management: dazu zählt Auswahl, Bewertung,Dokumentation,Monitoring, Audits sowie regelmäßiges Update der
experienced with working in projects • Design and change control processes in medical devices • ISO 9001 and ISO 13485 experience • Knowledge of quality controls needed for medical device manufacturing • Up to date knowledge of law and regulations (FDA’s 21CFR820, MDD/IVDD/AIMDD directives) and harmonized
connection with the develop of a strategic plant in Poland - Silesia we are looking for ambitious individuals for the position of Product Print Coordinator from Quality site. The person in this position will report to the Global Portfolio Director.DescriptionResponsible for the implementation of product
who embody positive energy and effective communication, who drive initiatives and who thrive on challenges. Poland remains one of the key country in CEE region and due to further development of the business, we are looking for an independent Clinical Research Associate (CRA) to join an international ...
necessary permits will be requested and approved Execute a design review and release workshop and report the result Be on site during construction and check quality on a daily base Your qualifications We expect that you have at least a Master's degree in Electrical or Mechanical or Civil. 5 years experience
supply chain managerial position at a multi-national company, preferably in automotive industry Knowledge and experience in world class level supply chain management methods and tools (lean, 5S, Kanban, WMS, JIT, VMI, consignment stock, etc.) Knowledge in automotive quality standards and requirements ERP