Document Control Specialist

1 month ago


Ramsey, United States Catalyst Life Sciences Full time

Opportunity to join a small medical device manufacturer that have been around for 30 years as they go through a period of increased sales. Joining a Quality team of 10, you'll be responsible for the documentation, eQMS, and training of new employees, trusted to make improvements when and where you see fit.


Main Responsibilities

  • Assist in ETQ software training and other training as required.
  • Ensure projects are completed accurately and on time.
  • Able to interact with internal and external customers.
  • Support Quality in both external and internal audits.


Experience Required

  • 3+ years' experience in a Document Control / Training role in the Medical Device/Pharmaceutical industry.
  • Understanding of an eQMS, and desire to make changes to improve existing processes
  • Ability to work onsite 3 times a week.


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