| 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 : | Second Shift Supervisor |
| Position vacant : | Second Shift Supervisor |
| Job location : | Hudson, New Hampshire |
| Job code : | JF |
| Job details | |
| Company name : | Atrium Medical |
| Minimum experience : | 1 years |
| Maximum experience : | 30 years |
| Job type : | Permanent |
| Gross pay : | Negotiable for the right candidate |
| Job posted : | Dec 04, 2006 |
| Job description | |
| Job description: | SECOND SHIFT SUPERVISOR (MFG) (JF)
Position Type Full Time Location Hudson, NH Date Posted 10/13/2006 Position Specific Requirements: To plan, organize, supervise and control the activities of the manufacturing department. Coordinate manufacturing methods, material and production requirements of medical devices and implants. Plan and schedule product shipments to be sterilized and acts as a liaison between the contract sterilizer and Atrium to coordinate product sterilization. Establishes and maintains Device History Records for all products manufactured. Participate in the review and disposition of manufacturing documentation. Provide input and feedback for improved manufacturing of products and development designs. Provide input and feedback for the work area layout and material flow of the manufacturing production line. Participate in weekly product development meetings. Work with Production Planner and Marketing to coordinate production schedule requirements. Perform other duties as required. Qualifications: Associates Degree in related field and/or High School diploma and four (4) years of directly related experience in a manufacturing environment. |
| How to apply : | Register to view |
| Third party mediation allowed : | No |
| Telecommute : | No |
