Job Location : Oneonta,NY, USA
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.