Quality Assurance Officer resume example with 20+ years of experience
Jessica
Claire
resumesample@example.com
(555) 432-1000,
Montgomery Street, San Francisco, CA94105
:
Professional Summary
Self-managing Quality Assurance professional with 20+ years of experience. Demonstrates ability to manage production-related processes affecting all production sites. Has built a strong reputation as a respected leader across all departments. Able to work with colleagues in cross-functional teams, self-managing teams, and project teams. Accomplishes goals in an expeditious manner. Assists in mentoring new employees to help them reach their full potential for the betterment of the entire team. Establishes and maintains strong relationships with suppliers. Known for accuracy, efficiency, attention to detail, and best-in-class work ethic.
Skills
ISO 13485 / ISO 9001 / MDSAP
Strong Leadership Experience
Internal and Supplier Auditing
SAP ERP System
GMP/GDP Proficiency
Staff Training & Development
Material Review Board
Clean Room Practices
Program/Project Management
Calibration Management
Supplier Management
Time Management
Mechanical Inspection
Blueprints & Technical Specs
Statistical Analysis
Lean Manufacturing Principles
Education
University Of Massachusetts - LowellLowell, MAExpected in 2000 ā āBachelors of Science:Business Administration - Management - GPA:
American Society For QualityOnline, Expected in ā āCertification - In-Process:CQM/OE, CQE, CQA - GPA:
Certifications
Internal Auditor Training for ISO 13485
Oriel STAT A MATRIX
Aug 2012 No Expiration Date
Credential ID 114945
Lean Communication: Connecting the Value Stream
Northern Essex Community College
Apr 2007 No Expiration Date
Lean Planning and Leadership
Northern Essex Community College
Apr 2007 No Expiration Date
Managing the Transformation to Lean Culture
Northern Essex Community College
Apr 2007 No Expiration Date
Work History
American Chemical Society - Quality Assurance Officer Merced, CA, 2012 - Current
Proficient in handling radioactive material while observing established safety regulations.
Authorizes release of approved final product and prevents release of suspect or known nonconforming product
Performs incoming inspections to specification and coordinates disposition of nonconforming materials.
Conducts internal audits to determine effectiveness of training, documentation and process.
Conducts supplier audits to assess and identify potential gaps in the supplier quality process
Manages several processes and projects essential to realization of department goals
Identifies need for CAPA actions and coordinates monthly NCR meetings
Organizes reports, files and results in a professional proficient manner.
Ensures all activities are performed in accordance with ISO13485 requirements
Cooperates with engineering, manufacturing and corporate accounting to verify adherence to quality standards.
Cornerstone Building Brands - Production Lead West Sacramento, CA, 2006 - 2012
Delegated and oversaw the completion of daily production requirements.
Supported customer source inspections and audits.
Handled production line documentation requirements, including waste, downtime and output.
Monitored workers on site during production activities for safety procedures compliance.
Identified and corrected defects to bring completed products in line with tolerances.
Trained new employees in assembly skills to improve team production levels.
Communicated clear instructions for general operations and product-specific runs to prevent errors and rework.
Monitored employee activities to verify consistent use of good manufacturing principles.
Trained workers in proper operation, calibration and maintenance of production line equipment.
Contributed to continuous improvement and lean initiatives by implementing directives.
Sustained tour-ready production line through continuous and effective housekeeping plans.
Determined root cause of deviations and non-conforming results and implemented appropriate corrective and preventive actions throughout product development process.
Documented and executed detailed test plans and test cases and summarized and logged audit findings for reporting purposes.
Reviewed and validated quality requirements for manufacturing planning, supplier purchase orders and engineering specifications to meet contract compliance regulations.
Inspected manufactured parts by reviewing visually and assessing dimensions.
Evaluated samples against standards by completing measurements, visual inspections and other established tests.
Interpreted test results by comparing to established specifications and control limits, making recommendations on appropriateness of data for release.
Abbvie, Inc - Quality Control Technician II Little Rock, AR, 2000 - 2003
Inspected raw materials and finished products to verify quality and disposed items that did not meet safety requirements.
Performed visual assessment of products to evaluate conformance with quality standards.
Conducted investigations into questionable test results.
Completed supporting documentation for testing procedures, including data capture forms, equipment logbooks and inventory forms.
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