Technical Resources International, Inc.
Quality Assurance Specialist
Technical Resources International, Inc., Bethesda, Maryland, us, 20811
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Quality Assurance Specialist
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Technical Resources International, Inc.
Considering making an application for this job Check all the details in this job description, and then click on Apply. This position supports the maintenance of the Quality Management System, manages QA training, document control, customer complaint, and CAPA programs, and assists with audits of clinical sites and vendors. The role also involves supporting internal audits, performance metrics, and regulatory agency audits. Job Responsibilities: Maintain and update the Quality Management System. Manage QA training, document control, customer complaints, and CAPA programs. Support audits of clinical sites, vendors, and regulatory agencies. Assist in internal audits and performance metrics for continual improvement. Review QA-controlled documents to ensure compliance with written procedures. Job Requirements: Knowledge of current GCP regulations. Experience with regulatory agency audits. Experience with Quality Systems for CROs. Excellent written and verbal communication skills. Proficiency in MS Office. Additional Details: Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industry: Pharmaceutical Manufacturing This job posting is active.
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Quality Assurance Specialist
role at
Technical Resources International, Inc.
Considering making an application for this job Check all the details in this job description, and then click on Apply. This position supports the maintenance of the Quality Management System, manages QA training, document control, customer complaint, and CAPA programs, and assists with audits of clinical sites and vendors. The role also involves supporting internal audits, performance metrics, and regulatory agency audits. Job Responsibilities: Maintain and update the Quality Management System. Manage QA training, document control, customer complaints, and CAPA programs. Support audits of clinical sites, vendors, and regulatory agencies. Assist in internal audits and performance metrics for continual improvement. Review QA-controlled documents to ensure compliance with written procedures. Job Requirements: Knowledge of current GCP regulations. Experience with regulatory agency audits. Experience with Quality Systems for CROs. Excellent written and verbal communication skills. Proficiency in MS Office. Additional Details: Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industry: Pharmaceutical Manufacturing This job posting is active.
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