Document Control Clerk II

Document Control Clerk II

Irvine, CA









ArthroCare Corp. (Nasdaq:ARTC) is a multi-business medical device company that develops products based on its pioneering Coblation(R) technology. The benefits of Coblation technology provide an answer to the challenges of soft tissue management in any surgical specialty where controlled and efficient ablation is of value. Current applications include: Arthroscopic Surgery, Spine Surgery, Dermatologic Surgery, Ear, Nose & Throat Surgery (ENT), and General Surgery.

Our greatest achievements come from our greatest assets: ArthroCare's employees. We are continuously seeking new talent to join ArthroCare's winning ranks. People who thrive at ArthroCare are passionate about improving surgical procedures and patient outcomes, have a competitive spirit and winning attitude, and place a high value on teamwork and trust. We offer a competitive benefits package and excellent opportunity for career development.



Summary: The purpose of this position is to provide engineering change notice (ECN) processing and administrative support for Document Control, Quality and Engineering departments. This position will support future growth within the Manufacturing, Engineering and Quality departments.



Essential Duties and Responsibilities include but are not limited to: (Other duties may be assigned)Provide timely and accurate processing of ECN's, including data entry, copying and filing for electronic document systems (Agile/SAP). Eliminate backlogs.Ensure approved data management is entered accurately in SAP in relation to Agile (ECN new releases and changes) and SAP master data inputs.Update Solid Works/CAD drawings per ECNs. Maintain labeling database system per ECNs. Provide the service of processing ArthroCare documentation from all groups to support business needs as required.Audit document satellite files (i.e.: Manufacturing, IQA, Engineering and Quality) to ensure all documentation is current.Assure compliance to US and International regulations (i.e. cGMP's/EN/ISO 13485/Japan) requirements. Effectively support and follow policies and procedures.



Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required.



Education and/or Experience:Requires a High School diploma.Minimum one (1) year previous medical device industry experience.Must have good computer, word processing, filing and communication skills.Minimum of one (1) year experience of Agile (ECN) and SAP (Master data management) required.Strong verbal and written communication skills as well as technical writing and documentation skillsStrong attention to detailRequires basic knowledge in required software for label generation.Solid Works/CAD experience required.Good knowledge of Word, Excel, and Access



Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the functions of the job.



For consideration of this and other opportunities please visit our career center at: http://careers.arthrocare.com





Equal Opportunity Employer
www.ArthroCare.com





Education: High SchoolJob Level: 1-3 Years