Senior Quality Engineer

Job Position: Senior Quality Engineer

Duration: 12 months

Location: Salt Lake City UT 84116 (Hybrid – 4 days onsite & 1 day remote per week)

Job Description:

• This position is accountable for supporting new product development and product maintenance through the application of Quality engineering skills for medical devices. This person will handle projects and tasks, from product inception through product launch and maintenance and play an active role in the processes to ensure products meet quality standards consistent with both Corporate and unit policies, while meeting all design control and other regulatory requirements.

Responsibilities:

• Consistent application of technical principles, theories, concepts, techniques and quality sciences/tools (e.g. 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.).
• 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.

Education and Experience:

• Requires a minimum of a bachelor’s degree.
• A minimum of 5 years relevant experience or a combination of equivalent education and relevant experience.
• Must have experience within the medical device or equivalent regulated industry.
• Working knowledge of statistical analysis and software use (Minitab preferred).
• Process validation experience (IQ/OQ/PQ).
• Design change experience including Design Controls/Design verification/Design validation/Risk management and Corrective and Preventive action.