Questions? 1-888-481-3375

Document Control Specialist (FDA/ Medical Device)

San Diego, CA

Apply Now

Description

RemX is currently looking for several Document Control Specialist for a top medical manufacturing company in San Diego. 

 

Salary Is DOE!

 

Duties:

  • Will ensure that changes and documentation follow the company policy and procedures
  • Conduct Change Control process in the quality system and track the change process through development, approval, and implementation
  • Adhere to commitment to the development, effectiveness, and implementation of the company’s QMS per FDA, ISO, and other regulatory agencies
  • Audits, classifies, receives, and tracks and maintains centralized documentation archiving systems of controlled Quality System documents
  • Will partner with other associates to meet compliance changes
  • Will assist with the preparation of legal documents for migration into an electronic document control system

Job Requirements

  • 2-6 years of relative work related experience in Document Control
  • High school diploma or GED
  • Must have FDA Medical Device industry background
  • Experience with federal and other regulations, e.g. QSR’s, ISO 13485, FDA, CMDR 

 

 

Don’t miss the opportunity to work for a top medical device manufacturing company.  Forward resumes ASAP.

 

Key Words:

Document Control, Specialist, Technician, Clerk, FDA, Medical Device, QC, Quality Control, QA, Quality Assurance, Documentation

QMS, ISO, 13485, 21 CFR, Inspector, Inspecting, Change Orders, Agile, SAP,

Apply Now