IS Document Control Specialist
Location: Plainsboro New Jersey
Description: Integra Life Sciences is at present recruited IS Document Control Specialist right now, this occupation will be placed in New Jersey. More details about this occupation opportunity kindly read the description below. Company Description
Integra LifeSciences , a world leader in medical devices, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedics, neurosurgery, spine, reconstructive and general surgery. Integra's orthopedic products include devices and implants for spine, foot and ankle, hand and wrist, tendon and peripheral nerve protection and repair, and wound repair. Integra is a leader in neurosurgery, offering a broad portfolio of implants, devices, instruments and systems used in neurosurgery, neuromonitoring, neurotrauma, and related critical care. Integra is also a leading provider of surgical instruments to hospitals, surgery centers and alternate care sites, including physician and dental offices. Founded in 1989, Integra is headquartered in Plainsboro, New Jersey and has over 3,000 employees worldwide. For the last three years, Integra has been included in NJBIZ's list of 'New Jersey's 50 Fastest Growing Companies.' In 2010, we were also included in Forbes magazine's 'America's 100 Best Small Companies'. We value innovative thinkers who are open to new opportunities and derive satisfaction from knowing that their efforts are making a difference in someone’s life. Detailed Description
As part of Integra the IS Documentation Specialist will be responsible for developing, and maintaining the documentation program for the IS Dept. The candidate must be successful in handling compliance documents including validation plans, test plans, design documents, test scripts and traceability matrix. This involves working in a team environment and taking a lead role in the documentation area.
SUPERVISION RECEIVED Supervision will be provided by the Director of IS Process and Compliance.
SUPERVISION EXERCISED No direct staff but may supervise contractors as assigned.
ESSENTIAL DUTIES AND RESPONSIBILITIES
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Ensure controlled documents are appropriately reviewed and approved prior to implementation via the document change control process. Validation liaison for the routing and approval of validation documentation consisting of high volume of documents with strict deadlines in a fast paced environment. Coordinate execution, approval and archival of System and UAT test scripts. Assembly, maintenance and archival of Validation and SDLC documents. Maintain various logs associated with archival of validation documentation. Create and revise controlled documents; Ensure changes are properly documented. Store and distribute various document requests to departments as needed. Assist with preparing and organizing documents for offsite storage archival. Maintain storage logs. Assess training files and folders of IS resources and consultants for accuracy and details. Travel to other Integra sites or locations during project or system implementation. Other duties as assigned
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If you were eligible to this occupation, please email us your resume, with salary requirements and a resume to Integra Life Sciences.
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This occupation starts available on: Thu, 05 Jul 2012 08:31:28 GMT