Description:
This position requires verification of compliance to applicable Standard Operating Procedures (SOPs) and GLP regulations (21 CFR Part 58) by performing study protocol, data, report, and in-life phase inspections, where applicable. Candidate will participate in the conduct of internal facility/process and Quality System inspections, maintain inspection records, assist with CAPA activities and assist with the review of documentation supporting equipment qualification and change control activities.
At least 1 year of experience working in a regulated environment, strong attention to detail, data integrity and compliance, excellent communication and interpersonal skills. Experience working in the CRO/Pharma/Medical Device industry highly preferred. TB Testing and Immunization Shots. Capable of working in an animal environment.
Minimum Requirements: A Bachelor’s in Science, (Chemistry, Microbiology Pharmacy or Engineering).