Design Quality Reliability Engineer II - Med Devices

Planet Pharma; Minneapolis (MN); On-site; USD 90,000 - 130,000; Full time

Job summary

Planet Pharma is seeking an experienced reliability engineer in Minnesota to lead design assurance, reliability testing, and quality activities for medical devices. Responsibilities include conducting reliability studies, performing DOE, and executing risk analyses to ensure regulatory compliance and product performance.

The role requires a bachelor’s degree and at least 2 years in quality or reliability within medical devices, plus ability to work with cross-functional teams and manage multiple

Qualifications

• Requires a Baccalaureate degree and minimum of 2 years of relevant experience.
• Experience in reliability engineering or quality in medical devices is expected.
• Familiar with design of experiments (DOE) and reliability testing methods.

Responsibilities

• Develops, coordinates and conducts technical reliability studies and DOE constructs.
• Recommends design or test methods and SPC procedures for reliability.
• Completes risk analysis studies of new design and processes.
• Analyzes performance reports and statistics; investigates variables affecting products and processes.
• Ensures corrective measures meet reliability standards and documentation is compliant.
• Develops reliability programs to meet objectives and may model failure risks.
• May determine units/batches requiring environmental testing and sample sizes.

Skills

Design Assurance/Design Quality/Reliab

General quality experience in med

Education

Bachelor's degree in a related field

Job description

Planet Pharma is seeking an experienced reliability engineer in Minnesota to lead design assurance, reliability testing, and quality activities for medical devices. Responsibilities include conducting reliability studies, performing DOE, and executing risk analyses to ensure regulatory compliance and product performance.

The role requires a bachelor’s degree and at least 2 years in quality or reliability within medical devices, plus ability to work with cross-functional teams and manage multiple