better Job at VNUS Medical Technologies Inc

Buyer/Planner Temporary Responsibility and Authority Manage all aspects of the material acquisition process, including MRO R&D, tooling, and components. Planning for long-range blanket orders for MRO and components, purchase order strategy, and tactical supply details such as safety stock, lead time, packaging, JIT, etc. Have working knowledge of purchasing raw components required for FDA regulated manufacturing environment. Negotiate purchase orders, to meet

Materials Coordinator - Temporary The Materials Coordinator is responsible for coordinating the shipping and receiving of all material and products, maintaining an accurate inventory, and performing the required transactions to document the activities in MFG/PRO. Overall Responsibilities Shipping and receiving of all materials entering or exiting the building. Maintaining shipping, receiving and finished goods areas in a clean and orderly fashion. Shipping

Clinical Specialist - Denver, CO or Salt Lake, UT Responsibility and Authority: Training and educating VNUS customers on our products. Selling VNUS Medical Technologies products in the United States to established accounts. Scope of Duties / Job Description: Product training for all potential audiences involved in the use and sale of the Closure System including but not limited to: General and Vascular Surgeons, Dermatologists, Interventional

Responsibility and Authority: The Director of Clinical Research, in coordination with his/her European counterpart, has the responsibility for the strategic planning, tactical implementation, and reporting of clinical investigations involving human subjects. Scope of Duties / Job Description: Proposes options for alternative study designs and methodology. Work with senior management in solving problems and addressing changing clinical study and market opportunities. Reviews publications

Director of Quality Assurance Responsibility and Authority: The Director of Quality Assurance has the authority and responsibility for ensuring that the requirements of 21 CFR Part 820 and ISO 13485 are implemented and maintained. Scope of Duties / Job Description: The Director of Quality has the authority and responsibility for the quality system compliance to 21 CFR Part 820 and ISO 13485:2003 Prepares for and conducts the management review with Senior Management to ensure

Responsibility and Authority: The Quality Engineer has the authority and responsibility for: Addressing product-related quality problems Controlling further processing, delivery or installation of non-conforming product until the deficiency or unsatisfactory condition has been corrected Initiating, recommending, or providing solutions through designated channels Initiating action to prevent the recurrence of product nonconformities Verifying the adequacy