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Location: Mahwah, NJ Description: Our client is currently seeking a RAQA Specialist for a 12 month + contract.
Description/Comment: Responsible for routing and organizing quality manual, procedures (SOP), policies, guidelines, checklists, work instructions, training documents. Organizing global, corporate and site level documents like work instructions, procedures, validations, reports, BOMs, standard forms and lists into electronic document management system (Master Control). Ensure documents comply to ISO, FDA requirement standards. Update department policy and procedure documents to reflect recent process changes. Issues, expedite and maintain control of final and revised prototype and production release documents. Maintain online document management system and stay up to date on new versions and training. Track and follow-up on renewal of expired documents from vendors, inspections and audit records. Support auditing with the requested documents and records. Support merger and acquisition integration for Wright Medical integration into Stryker T&E. Lead and/or assist with process improvements pertaining to Quality Systems. Technical background not needed. Associates Degree or equivalent work experience required. Formal training and on-the job experience using Microsoft Office suite technology, including Word, Excel and PowerPoint. Prefer training in Access or other complex data management program/system. Provide the full spectrum of administrative support to one or more departments/functions.Additional Job Details: Can be onsite or remote, please include candidates current location on their resumeContact: This job and many more are available through The Judge Group. Find us on the web at www.judge.comVacancy expired!