Focused and methodical professional offering expertise in inspecting, testing and quality monitoring of materials. Demonstrated success in upholding standards, monitoring safety and promoting production excellence. Experienced in producing detailed reports and maintaining thorough records.
Highly-motivated employee with desire to take on new challenges. Strong work ethic, adaptability, and exceptional interpersonal skills. Adept at working effectively unsupervised and quickly mastering new skills.
Overview
12
12
years of professional experience
Work History
Medical Device Quality Inspector Team Lead Tech
Zeus Industrial Products Inc
Gaston, SC
11.2017 - 09.2025
Reviewed product designs for manufacturability issues that might affect overall product quality or reliability.
Reviewed engineering documents such as drawings, schematics, work instructions, and process validations related to the manufacture of medical devices.
Monitored assembly processes and equipment performance to identify potential problems or areas for improvement in product quality.
Inspected products at various stages during the manufacturing process to ensure quality standards are met.
Assisted in root cause analysis investigations into identified nonconformances or defective products.
Analyzed test data from medical device components, assemblies and systems to determine conformance with established requirements.
Participated in internal audits of Quality Management System processes as a member of the audit team.
Developed acceptance criteria based on industry standards or customer specifications for use in evaluating manufactured products.
Conducted incoming inspection on all raw materials, parts and sub-assemblies for medical devices.
Maintained traceability records between raw materials used in the production process and finished goods produced by the facility.
Performed detailed inspections of medical device components to ensure compliance with required specifications and standards.
Trained junior inspectors on proper inspection techniques and equipment use.
Assisted in the development of quality control procedures and guidelines.
Participated in cross-functional meetings to discuss quality improvement initiatives.
Verified accuracy of documentation related to the production of medical devices.
Investigated customer complaints regarding product defects and nonconformities.
Provided guidance and training to personnel involved in manufacturing operations concerning proper techniques used when inspecting products.
Prepared reports summarizing findings from inspections conducted on medical device components or assemblies.
Documented results of quality control activities in accordance with established procedures.
Interpreted technical drawings, diagrams and other engineering documents related to medical devices design and manufacture.
Inspected, tested and measured materials for conformance to specifications and regulatory requirements.
Learned new testing methods through continued education and research.
Made adjustments to equipment or calibrated instruments to required tolerances.
Conducted regular performance assessments to provide feedback and support development.
Trained new employees on safety protocols and operational procedures.
Facilitated communication between departments to resolve operational issues quickly.
Provided guidance and direction to subordinates regarding job duties and responsibilities.
Resolved customer complaints in a timely manner while ensuring customer satisfaction.
Monitored employee productivity to provide constructive feedback and coaching.
Developed and implemented operational policies and procedures to ensure efficiency and accuracy of workflows.
Trained new employees on company policies and procedures.