Duration: 9+ Months

Top/Required Skills:

- Associates or Bachelors and minimum of 2 years relevant work experience, preferably in a manufacturing environment

- Previous experience using ETQ or other Document Management software preferred

- Proficiency in Microsoft office

- Experience in ISO 9001 or other Quality System standards

- ISO 13485 and 21 CFR 820 Quality Management Systems knowledge highly preferred

- Extremely organized with ability to use multiple resources in comparing documentation

This position is to assist with a major project in Oneonta with changes to the documentation system and preparing for an audit.

Summary:

Responsible for administration of quality management system documents and records required for Life Sciences processes. Responsible for initiation of document changes, distributions, notifications and fulfilling internal and external document distribution.