Document Control Specialist

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.