| 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 : | Program Manager Endovascular |
| Position vacant : | Program Manager Endovascular |
| Job location : | hudson, New Hampshire |
| Job code : | PME PM |
| Job details | |
| Company name : | Atrium Medical |
| Minimum experience : | 7 years |
| Maximum experience : | 28 years |
| Job type : | Permanent |
| Gross pay : | Negotiable for the right candidate |
| Job posted : | Dec 04, 2006 |
| Job description | |
| Job description: | PROGRAM MANAGER OF ENDOVASCULAR SYSTEMS - PM
Position Type Full time Location Hudson, NH Date Posted 10/4/2006 Position Specific Requirements: Coordinate the design and development of medical devices and components. Support Sales and Marketing in defining market and customer needs and in developing a business plan. Provides technical support to Sales and Marketing, Quality and Regulatory, Product Development, and Manufacturing. Interacts with other groups to meet department objectives. Ensures regulatory compliance in product development, including coordinating design control and review process. Helps direct and review laboratory and clinical research. Serves as program leader and manages program resources. Evaluates patents for specific technology areas and coordinates filing patents as required. Collaborates with outside contacts and evaluates outside technology for use in meeting program objectives. Coordinates and run program meetings. Participates in negotiation of business transactions with outside parties. Assist with publications and presentations at technical symposia. Develops vendor contracts and specifications. Reviews progress with senior management. Performs other related duties as required. Qualifications: Bachelors degree in a technical field with 7+ years of relevant experience developing medical products. Working knowledge of medical device industry, FDA regulations, quality systems, and sterilization. Experience leading the development and implementation of projects, with ability to handle multiple projects and effectively manage timelines. Demonstrated analytical and problem solving skills. Ability to work independently, as well as effectively interact and communicate with all levels of the organization in a team environment. Proficient oral and written communication skills; technical writing experience and experience with Microsoft Word, Excel and PowerPoint. Oracle experience preferred. |
| How to apply : | Register to view |
| Third party mediation allowed : | No |
| Telecommute : | No |
| Travel required : | none |
