Doc Control Specialist

Location: Brooklyn Park, Minnesota Salary: competitive
Sector: Medical Devices, Quality Assurance (QA), Operations, R&D Type: Contract

Are you passionate about Documentation within the Medical Device Industry? Are you also interest in working with an amazing company that offers great opportunities? Well I have the right job for you! My client is now looking to hire a Doc Control Specialist. This person will be very experience with Engineering Change Orders, Manufacturing Change Requests, Deviation, and Documentation Life Cycle. The role is a 6 months contract with the possibility to be hired on permanently.

The Doc Control Specialist requires everything from maintaining/improving the engineering documentation systems while meeting cGMP and GDP standards.

Among others, the Doc Control Specialist will have the following responsibilities:

  • Engineering Change Orders
  • Manufacturing Change Request
  • Deviations

The most desirable candidates will possess the following qualifications:

  • 3+ years Doc Control within Medical Device
  • Knowledgeable with cGMP, GDP, ISO 9001, and ISO 13485
  • Excellent reading, writing, communication, and organizational skill

This is a wonderful opportunity to join a medical device company that offers great development.

If you are interesting in the Doc Control Specialist opportunity, please forward your current resume and/or contact me on the details below!

Sthree US is acting as an Employment Business in relation to this vacancy.