Job Details

ID #46060181
Estado Illinois
Ciudad Vernonhills
Tipo de trabajo Contract
Salario USD Depends on Experience Depends on Experience
Fuente Cynet Systems
Showed 2022-09-28
Fecha 2022-09-27
Fecha tope 2022-11-25
Categoría Etcétera
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Document Control Specialist

Illinois, Vernonhills, 60061 Vernonhills USA

Vacancy caducado!

We are looking for

Document Control Specialist for our client in

Vernon Hills, IL

Job Title: Document Control Specialist

Job Location: Vernon Hills, IL

Job Type: Contract

Job Description:

Responsibilities:
  • Serve as the Electronic Document Management System (EDMS) and Learning Management System (LMS) administrator (e.g., maintain accurate users, assign passwords and privileges, update training requirements, etc.).
  • Ensure timely, accurate, and efficient preparation and management of documents.
  • Control the numbering, sorting, filing, storing, and retrieval of both electronic and hard copy documents.
  • Process changes via the EDMS and DCN systems.
  • Provide database navigation and troubleshooting support for the EDMS, LMS, and paper-based DCN system).
  • Assist managers to ensure required training is assigned and documented
  • Update Product Database.
  • Provide documentation and training compliance metrics as requested
  • Maintain central device master documentation.
  • Maintain records in accordance with record retention policies.
  • Interface with internal and external auditors during the review of the applicable quality management sub-systems (i.e., those pertaining to documentation, change control, and training).
  • Continuous improvement of the change control, documentation control, and training systems.
  • Successful completion of projects assigned by management to support business imperatives.
  • Other duties as assigned.

Qualifications, Knowledge, and Skills Required:
  • Associate degree preferred high school diploma or equivalent required.
  • Excellent verbal and written communication skills.
  • Strong collaboration across business functions.
  • Ability to aggressively drive results in multiple projects simultaneously.
  • Use of Microsoft Office software to generate formal procedures, control logs, and databases.
  • Two years of relevant work experience required, preferably in a regulated medical device or pharmaceutical environment.
  • Understanding of blueprints, standard operating procedures, and overall documentation systems.

Vacancy caducado!

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