URL blocked - click to applyFounded in 1979, Technical Resources International, Inc. (TRI) is a full-service contract research organization plus (CRO+) providing product development support services to the global drug, biologic, and medical device community through the effective combination of scientific, clinical information technology, and communications services. TRI, Inc. is currently seeking a Quality Assurance Specialist.
Responsible for verifying compliance to applicable Standard Operating Procedures (SOPs) and regulations by performing internal audits. Promotes quality by preparing Project Specific Procedures, providing training to staff and supporting the Quality Management System. Responsibilities may also include hosting client audits, conducting external audits at clinical sites and vendor sites, leading process improvement activities and leading CAPA investigations. Conducts quality-focused trainings via Web-Ex and face-to-face sessions.
Minimum a BS/BA, a Masters’ Degree desired but not required. 3-5 years of progressive QA experience preferably in a CRO environment. A solid understanding and working knowledge of GCP (minimum 5 years). Experience working with Quality Management Systems. Training experienced via Web-Ex or face to face. Proficiency in MS Office. Travel up to 30%.
Technical Resources International is fully committed to Equal Employment Opportunity and to attracting, retaining, developing and promoting the most qualified employees without regard to their race, gender, color, religion, national origin, age, physical or mental disability, veteran status, or any other characteristic prohibited by state or local law.
Total Quality Management
Provide Technical Guidance