The QA Auditor will be responsible for monitoring each GLP study to assure management that the facilities, equipment, personnel, methods, practices, records and controls are in conformance with the GLP regulations, 21 CFR Part 58).
More responsibilities include are listed below:
- Assessing Vendors for GLP Compliance and monitoring studies performed at the vendors
- Assessing sites for compliance to the Policy on Animal Welfare Providing audit reports for audits / assessments performed.
- Working across the Medical Device companies to provide Compliance Oversight and training to internal personnel on GLP Sponsor Responsibilities
- Assisting as necessary with the internal GLP activities to conform with the GLP regulations across the medical device community
BS or equivalent degree with experience in the area of laboratory animal sciences or related subjects with some level of training & experience related to GLP, FDA (Food & Drug Administration) & USDA (United States Department of Agriculture) processes
Associate degree with experience in the area of laboratory animal sciences or related subjects & certification as a Laboratory Animal Technologist or Registered Veterinary Technician with training & experience related to GLP, FDA & USDA processes. Associate degree should have 10+ years' experience in laboratory animal sciences or related subjects.
If you are interested in the position, please apply as soon as possible. The Manager is actively scheduling interviews.
Sthree US is acting as an Employment Business in relation to this vacancy.