CANDIDATUL IDEAL:
At least 3 years in managing technical personnel and complex activities (areas of engineering or technical operations) and a minimum of 1 year in quality management;
Technical University degree;
Excellent communication skills and speaking English fluently;
Theoretical and practical knowledge with ISO Quality System Regulations and Guidelines and related quality standards;
Practical experience with DFM, Risk management assessment, FMEA, Product testing, Capability studies and Control plans;
Knowledge of Six Sigma techniques and Lean Manufacturing is an advantage. |
RESPONSABILITATI / BENEFICII:
Providing leadership for developing and directing Quality Assurance and Quality improvement initiatives (COQ reduction, Audit system, etc.) for all products and services;
Initiates and coordinates creation, implementation and living of the quality plan to bring the Company into ISO 9000-2000 and ISO 14001 compliance;
Controls the quality plan efficiency and acts permanently for its improvement and designs cost reduction activities by integrating quality (Six Sigma) tools in the process;
Maintains all the necessary documentation related to Quality system, ISO and other industry guidelines;
Organizes and takes part in the internal and external Audits and assesses improvement initiatives resulting from all Quality Audits;
Manages and maintains an Approved Suppliers Quality Program, utilizing suppliers audits, statistical control programs, suppliers checklists, and mechanisms to monitor supplier delivery and quality trends to assure that best vendors are qualified and retained;
Manages and maintains the Company's quality inspection and product release programs for incoming and inprocess materials and components, clinical products, and finished goods.
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