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R&D/Released Product Engineer II - CST - Memphis, TN (Onsite)

Medtronic

Memphis, TN, US$89k – $133konsite

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About this role

We anticipate the application window for this opening will close on - 22 Aug 2026   Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life At Medtronic Neuroscience, we bring innovation, expertise, and purpose together to improve care for people living with neurological, spinal, and chronic pain conditions. Our technologies help restore function, improve quality of life, and support better outcomes for patients around the world.                     Medtronic Cranial & Spinal Technologies is transforming complex spine and cranial surgery through connected, precision-driven technologies. From implants and robotics to navigation, imaging, advanced energy, and digital solutions, we empower surgeons to make confident decisions, perform with greater precision, and help improve outcomes for patients.

Check us out on LinkedIn: Medtronic CST

The R&D/Released Product Engineer II plays a key role in supporting medical devices throughout the product lifecycle, from commercialization through end-of-life. This position is responsible for designing, developing, and improving products while ensuring compliance with applicable regulatory, quality, and manufacturing requirements. The role partners closely with cross-functional teams to execute sustaining engineering initiatives, product enhancements, change management activities, verification and validation efforts, risk management activities, post-market support, and manufacturing transfers. The ideal candidate demonstrates strong engineering fundamentals, sound technical judgment, and the ability to independently execute engineering assignments while collaborating effectively across multidisciplinary teams

Responsibilities may include the following and other duties may be assigned: • Support released products throughout the commercialization-to-end-of-life product lifecycle.

• Execute sustaining engineering projects, product improvements, and design changes that support quality, compliance, manufacturability, and business objectives.

• Develop engineering solutions using sound technical principles, engineering analysis, and risk-based decision making.

• Collaborate with cross-functional partners including Quality, Regulatory Affairs, Manufacturing, Operations, Marketing, Medical Affairs, and Supply Chain to achieve project objectives.

• Support design control activities including product requirements, design reviews, verification, validation, and design transfer.

• Participate in product risk management activities, including hazard analysis, risk assessments, and mitigation planning.

• Develop and implement engineering change orders, product updates, and manufacturing improvements while maintaining compliance with applicable procedures and regulations.

• Provide technical support for post-market activities, product investigations, quality initiatives, and customer-facing issues.

• Support manufacturing transfers, supplier changes, and process improvement initiatives to ensure product quality and continuity of supply.

• Prepare and review technical documentation, protocols, reports, specifications, and engineering assessments in accordance with quality system requirements.

• Contribute technical expertise to project teams and actively participate in problem solving and continuous improvement initiatives.

• Effectively communicate technical information and project status to stakeholders across multiple functions.

Minimum Requirement (Must Haves): • Bachelors degree in Biomedical Engineering or Mechanical Engineering with minimum of 2 years of relevant experience

• OR, Advance degree in Biomedical Engineering or Mechanical Engineering with 0 years of relevant experience

• Experience supporting products within regulated industry

• Knowledge of engineering fundamentals, design controls, verification and validation, and risk management principles

Nice To Have: • Medical device industry experience

• Experience supporting implantable or capital medical device technologies.

• Knowledge of FDA, ISO 13485, EU MDR, and other applicable medical device regulations.

• Experience with design controls, verification, validation, and product risk management.

• Experience with sustaining engineering, post-market support, and product lifecycle management.

• Experience supporting manufacturing transfers, supplier changes, and process validation activities.

• Experience with PLM systems, CAD tools, and engineering documentation systems.

• Knowledge of additive manufacturing, tolerance analysis, or advanced manufacturing technologies.

• Experience working in a highly matrixed, cross-functional organization.

• Demonstrated ability to manage multiple priorities in a fast-paced environment

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be indepen

Salary insight

The midpoint of this range ($111k) is about 6% below the median disclosed salary for Memphis roles listed on ForgeApply ($119k across 92 jobs).

Based on live postings with disclosed pay on ForgeApply; refreshed daily. Not an estimate of this employer's offer.

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