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Document Control Specialist

Hours : Full Time
Travel : No
Relocation : No

Job Description :

Are you looking for an opportunity to continue to grow your career in the Medical Device Industry?  Our client is looking for a Document Control Specialist. 


 


Schedule:  1st Shift, M-F, 40 hours (3-6 month Temp/ Contract)


 


In this role you will be responsible for, but not limited to:



  • Process SOP, QAP, and Analytical forms for the Production Dept

  • Prepare training documentation

  • Maintain the QA Retain Management System

  • Data Entry year end data for company reports

  • Review, Prepare and Data Entry ECO's

  • Prepare for client, customer, ISO and FDA audits

  • Data Entry training documentation data into our Access data base

  • Prepare Certificate of Analysis and Certificate of Conformance

  • Inspect and Data Entry of incoming raw materials/chemicals

  • Inspect and Data Entry of finished product


 

 

Required Qualifications :


  • HS Diploma or equivalent

  • 3+ years experience with document control processes in the Medical Device Industry

  • Previous Training in ISO 9001, ISO 13485:2003, GMP, cGMP – A Plus!

  • Ability to work independently

  • Strong interpersonal skills

  • Ability to manage multiple tasks

  • Detail-oriented

  • Proficient w/ Microsoft Office Products (Outlook, Word, Excel, Access)


 


 
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