QA Document Control

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for an QA Document Control to work for a leading Orange County Area Medical device/Biotech company.
 

QA Document Control


Basic Function:
Compile and maintain control records relating to label issuance. Printing of production labels for manufacturing, assembly of batch records (DHR) for all production departments.  Verify all documents including formulations, manufacturing protocols and Bill of Materials prior to lot folder assembly. Maintain label inventory, word process of control documents. Support Document Control program.
 
Job Duties:
  • Compile and maintain control records relating to label issuance. 
  • Printing production labels for manufacturing (managing work schedules)
  • Assembly of Lot Folders for all departments (managing work schedules)
  • Verification of all documents prior to lot folder assembly
  • Maintain inventory of all label and ribbon stocks
  • Support document control program.
 
Experience/Education:
  • A minimum of two (2) years administration experience in a Quality Assurance Document Control medical device manufacturing environment or equivalent.
  • Experience with Weber Labeling Systems.
  • Computer skills, specifically MS Word, Excel, Outlook
  • Graphic design knowledge a plus.
  • Ability to speak, read, and write English.
  • Good oral and written communication skills.
  • Proficient in Word, Excel, PowerPoint, Outlook
 
If interested, please contact Drew Stephens at (562)495-3200 x2 or send him a copy of your most updated resume at drew@biophaseinc.com. Please visit www.biophaseinc.com for additional jobs as well.
 

  • Location: Orange County
  • Type: Contract
  • Job ID: HS233421214