| Company profile |
| Founded in 1981, Atrium is a privately held healthcare products company located in Hudson, NH. Atrium is a market leading manufacturer of breakthrough medical device technologies used in open heart surgery, emergency chest trauma, thoracic drainage and surgical repair of diseased blood vessels. More recently, Atrium is known for its high technology presence in coronary stents, minimally invasive intervention of peripheral blood vessels, state-of-the-art hernia repair, drug delivery research, hemodialysis access, and market leadership in facial plastic surgery. Atrium manufactures over 1,000,000 sterile medical products each year which are distributed to over 60 countries. Maintaining a commitment to innovation in research, market development and manufacturing has enabled the company to excel in many global medical device markets. With more than two decades of experience, Atrium has been an innovator of new technologies designed to meet the clinical needs of the patient. Whether it is chest drainage, drug delivery, drug coated stents, or new ways to deal with vascular disease and general surgery, Atrium is working on a new and innovative ways to solve unmet clinical needs. Atrium offers a unique opportunity with exciting challenges for the qualified candidate. |
| Job details | |
| Job industry : | Biotechnology/Pharmaceutical |
| Job segment : | General |
| Job role : | Other |
| Job skill : | Product Development Engineer |
| Position vacant : | SR. PRODUCT DEVELOPMENT ENGINEER-ENDOVASCULAR SYSTEMS PDE-JL |
| Job location : | Hudson, New Hampshire |
| Job code : | SPDE-Vascular JL |
| Job details | |
| Company name : | Atrium Medical |
| Minimum experience : | 7 years |
| Maximum experience : | 25 years |
| Job type : | Permanent |
| Gross pay : | Negotiable for the right candidate |
| Job posted : | Aug 31, 2006 |
| Job view count : | 458 |
| Job description | |
| Job description: | Position Specific Requirements:
Provide technical and project leadership over complex design, development and research projects particular to disposable endovascular systems. Responsible for the direct supervision and management of engineering personnel as needed. Responsible for achieving project and engineering objectives as specified by the Management Team by promoting investigation, inventiveness and creativity in the areas of polymer/material selection, processing and application toward development of stent delivery systems or related products. Maintain compliance to all Regulatory Standards for project and personnel safety. Recommend the addition, expansion or termination of engineering and research projects. Assure the technical soundness of engineering programs. Provide technical presentation support and consultation to marketing. Prepare project requests detailing proposed work costs and timetables. Analyze and translate experimental results into design criteria. Evaluate and select optimum design alternatives. Provide application-engineering support to customers. Develop potential applications to exploit new business opportunities. Collect and analyze information on competitive products. Assist in developing engineering budgets. Evaluate competitive patents and recommend alternative options. Vendor contract and specification development. Prepare reports and document progress with senior management. Perform other related duties as required. Qualifications: Bachelor degree or Masters degree (preferred) in Mechanical Engineering or related field with 7+ years experience. Good technical, leadership and interpersonal skills. Ability to manage resources, development programs and personnel. Experience with medical product development and regulatory requirements. Endovascular product development experience preferred. |
| How to apply : | Register to view |
| Third party mediation allowed : | No |
| Telecommute : | No |
| Travel required : | No |
