Location
Type
Status
Open
Lewisville, TX
Full-time
Full Job Description
Under general supervision, responsible for maintaining the VSP quality management system which includes calibration, document control, audit, supplier management, complaint, and quality management review. Takes a lead role in working with laboratory management to ensure compliance and regulations are being followed.
Responsible for periodic review of department internal control procedures; periodically review production processes in order to identify and recommend process improvements that improve quality, increase efficiency, and/or reduce waste
Interpret and assist with the implementation of quality standards
Review quality assurance standards, study existing policies and procedures, and interviews personnel and stack holders to evaluate the effectiveness of the quality assurance program
Perform quality-assurance functions to accomplish business coordination, monitoring, and reporting of quality-assurance studies according to the QA control plan
Assist with compiling data and writing narrative reports summarizing quality assurance findings; assist with control document revisions and maintaining the current revision level
Administer VSP quality management system for the laboratory, including calibration, document control, audit, supplier management, complaint, and quality management review
Review testing, quality control, and other testing reports for accuracy, completeness, and compliance to requirements to ensure that quality assurance standards and regulatory requirements are met
Keep management informed of quality-related activities in progress and discusses quality issues and completion of audit procedures
Maintain current and accurate records of all relevant communications, audits, corrective/preventative action plans, and process effectiveness monitoring
Job Specifications
Typically has the following skills or abilities:
Two to Four years of experience in manufacturing and/or production environments
Proven ability to effectively plan and execute audit assignments, including documentation of audit approach and findings
Ability to research processes, analyze problems, and define a system or procedural solutions
Full-time
Full Job Description
Under general supervision, responsible for maintaining the VSP quality management system which includes calibration, document control, audit, supplier management, complaint, and quality management review. Takes a lead role in working with laboratory management to ensure compliance and regulations are being followed.
Responsible for periodic review of department internal control procedures; periodically review production processes in order to identify and recommend process improvements that improve quality, increase efficiency, and/or reduce waste
Interpret and assist with the implementation of quality standards
Review quality assurance standards, study existing policies and procedures, and interviews personnel and stack holders to evaluate the effectiveness of the quality assurance program
Perform quality-assurance functions to accomplish business coordination, monitoring, and reporting of quality-assurance studies according to the QA control plan
Assist with compiling data and writing narrative reports summarizing quality assurance findings; assist with control document revisions and maintaining the current revision level
Administer VSP quality management system for the laboratory, including calibration, document control, audit, supplier management, complaint, and quality management review
Review testing, quality control, and other testing reports for accuracy, completeness, and compliance to requirements to ensure that quality assurance standards and regulatory requirements are met
Keep management informed of quality-related activities in progress and discusses quality issues and completion of audit procedures
Maintain current and accurate records of all relevant communications, audits, corrective/preventative action plans, and process effectiveness monitoring
Job Specifications
Typically has the following skills or abilities:
Two to Four years of experience in manufacturing and/or production environments
Proven ability to effectively plan and execute audit assignments, including documentation of audit approach and findings
Ability to research processes, analyze problems, and define a system or procedural solutions
Lewisville, TX
Full-time
Full Job Description
Under general supervision, responsible for maintaining the VSP quality management system which includes calibration, document control, audit, supplier management, complaint, and quality management review. Takes a lead role in working with laboratory management to ensure compliance and regulations are being followed.
Responsible for periodic review of department internal control procedures; periodically review production processes in order to identify and recommend process improvements that improve quality, increase efficiency, and/or reduce waste
Interpret and assist with the implementation of quality standards
Review quality assurance standards, study existing policies and procedures, and interviews personnel and stack holders to evaluate the effectiveness of the quality assurance program
Perform quality-assurance functions to accomplish business coordination, monitoring, and reporting of quality-assurance studies according to the QA control plan
Assist with compiling data and writing narrative reports summarizing quality assurance findings; assist with control document revisions and maintaining the current revision level
Administer VSP quality management system for the laboratory, including calibration, document control, audit, supplier management, complaint, and quality management review
Review testing, quality control, and other testing reports for accuracy, completeness, and compliance to requirements to ensure that quality assurance standards and regulatory requirements are met
Keep management informed of quality-related activities in progress and discusses quality issues and completion of audit procedures
Maintain current and accurate records of all relevant communications, audits, corrective/preventative action plans, and process effectiveness monitoring
Job Specifications
Typically has the following skills or abilities:
Two to Four years of experience in manufacturing and/or production environments
Proven ability to effectively plan and execute audit assignments, including documentation of audit approach and findings
Ability to research processes, analyze problems, and define a system or procedural solutions
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