Senior Quality Engineer 3 - Onsite (Req Exp in Medical Device)

Job Responsibilities

• Consistent application of technical principles, theories, concepts, techniques and quality sciences / tools.
• Acceptance sampling theory and application, statistical process control methods and application, measurement systems / test method knowledge and analysis.
• Quality planning, failure analysis and investigation, design of experiments, process mapping and value stream analysis.
• Hypothesis testing, descriptive statistics, process capability analysis, basic quality tools: pareto, box plots, histograms, scatter diagrams etc.
• Risk management, supplier quality management, auditing, design / development tools, process validation, software validation, etc.
• Handles projects and tasks, from product inception through product launch and maintenance.
• Writes, reviews, and approves protocols, reports, and data analysis.
• Ensures that all design control and production / process control projects meet applicable regulatory (local and international), Corporate, and Unit requirements.
• Reviews and has Quality Engineering approval authority for new and modified design / process specifications including product performance specifications, test methods, etc.
• Influences and/or directs others across organization and cross functionally.

Qualifications

• Requires a minimum of a bachelor’s degree.
• A minimum of 5 years relevant experience or a combination of equivalent education and relevant experience.
• Candidates must have experience within the medical device or equivalent regulated industry.
• Applied knowledge of applicable quality, engineering, regulatory, Corporate and/or Unit requirements.
• Proven problem-solving skills.
• Working knowledge of statistical analysis and software use (Minitab preferred).
• Basic use of risk management tools.
• General application of design controls.