Quality Assurance Specialist I or II

Ettevõte: Eurofins USA BioPharma Services
Töö iseloom: Full-time

Job Description
Basic Function and Scope of Responsibility: 
The position is primarily responsible for Quality Management System (QMS) activities and compliance with applicable regulatory requirements by ensuring the effectiveness of the QMS in meeting its stated goals and objectives. This position is also responsible for the management and maintenance of the electronic document management system, training and competency, and other systems and processes including training staff on document control processes and procedures.  This position will manage both paper and electronic records to ensure that controlled records are created, identified, changed, reviewed, retained, stored, and maintained in a manner that meets requirements. This position will support the laboratory with maintaining CLIA and other state permit accreditation, where applicable.

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