Sr. Advanced Manufacturing Engineer - New Product Development - Onsite

Showcify, Inc.; Jacksonville (FL); On-site; USD 102,000 - 154,000; Full time

Job summary

Medtronic is hiring a Senior Advanced Manufacturing Engineer - New Product Development in Jacksonville, FL. The role centers on creating and sustaining manufacturing processes and equipment for new products, with a focus on safety, quality, and cost objectives. Onsite four days a week in a regulated medical device setting.

You will lead validations, drive continuous improvements, and collaborate with Quality, Operations, and R&D to ensure successful product transfers and scale‑ups.

Qualifications

• Bachelor's or higher in engineering with relevant manufacturing exp.
• Experience with process validation and equipment qualification.
• Experience in regulated production environments.

Responsibilities

• Design, develop, and optimize manufacturing processes, equipment, and layouts.
• Lead process validation, equipment qualification, and readiness activities.
• Analyze manufacturing data and implement corrective actions.
• Develop and maintain manufacturing documentation.
• Collaborate with Quality, Operations, and R&D for transfers and improvements.
• Evaluate automation, tooling, and equipment enhancements.
• Apply SPC and data-driven decision making to monitor performance.
• Ensure compliance with regulatory, quality, and safety requirements.

Skills

Manufacturing engineering

Process validation

Equipment qualification

Lean manufacturing

Continuous improvement

Education

Bachelor's degree in engineering

Master's degree in engineering

PhD in engineering

Tools

SPC

Automation systems

Validation software

Job description

We anticipate the application window for this opening will close on - 6 Nov 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 outcomes and transform lives for people living with neurological, spine, and chronic pain conditions.

At Medtronic ENT, we deliver innovative technologies that help clinicians treat complex ear, nose, and throat conditions with greater precision and confidence. Our solutions enhance patient outcomes across both office and surgical settings.

Check us out on LinkedIn: Medtronic ENT

Medtronic’s ENT Operating Unit is dedicated to advancing surgical care through innovative technologies that enhance precision, efficiency, and patient outcomes. With a comprehensive portfolio that includes the StealthStation™ ENT Navigation System, M4 & M5 Microdebriders, and NIM™ Nerve Monitoring Systems, we empower surgeons with cutting‑edge tools for minimally invasive ENT procedures. Beyond technology, we are committed to clinical excellence, offering education, training, and research to support healthcare professionals. By continually pushing the boundaries of innovation, Medtronic is shaping the future of ENT surgery and improving patients' quality of lifeworldwide.

This position is based in Jacksonville, Florida and requires onsite presence 4 days/week.

The Senior Advanced Manufacturing Engineer - New Product Development, is responsible for developing, implementing, and sustaining manufacturing processes, equipment, and production systems that support safety, quality, delivery, and cost objectives. This role drives process improvements, supports new product and process introductions, investigates manufacturing challenges, and ensures compliance with applicable regulatory and quality requirements.

Primary Responsibilities

• Design, develop, and optimize manufacturing processes, production equipment, and workflow layouts to improve safety, quality, and operational efficiency.
• Lead process validation, equipment qualification, and manufacturing readiness activities for product and process changes.
• Analyze manufacturing performance data and implement corrective and preventive actions to address process variability and quality issues.
• Develop and maintain manufacturing documentation, including work instructions, process specifications, validation protocols, and standard operating procedures.
• Partner with Quality, Operations, and Research and Development teams to support product transfers, design changes, and continuous improvement initiatives.
• Evaluate and implement automation, tooling, fixtures, and equipment enhancements to increase productivity and process capability.
• Apply statistical process control methods and data‑driven decision making to monitor and improve manufacturing performance.
• Ensure manufacturing processes comply with regulatory, quality system, and safety requirements.

Required Qualifications

• Bachelor's degree with 4+ years of manufacturing engineering experience OR Master’s degree with 2+ years of manufacturing engineering experience OR PhD with 0+ years of experience required.
• Experience developing and sustaining manufacturing processes in a regulated production environment.
• Experience with process validation, equipment qualification, or manufacturing process development.

Preferred Qualifications

• Experience analyzing process performance data and implementing corrective actions.
• Experience collaborating with cross‑functional teams to support manufacturing operations and product quality.
• Experience in medical device manufacturing.
• Experience with Statistical Process Control (SPC) and process capability analysis.
• Experience supporting new product introduction, product transfer, or manufacturing scale‑up activities.
• Experience with Lean Manufacturing and continuous improvement methodologies.
• Experience with automation, tooling design, or advanced manufacturing technologies.

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 independently mobile. The employee is also required to interact with a computer, and communicate with peers and co‑workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise‑wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal‑level roles and above, where specialized expertise aligns with long‑term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits PackageA commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):$102,400.00 - $153,600.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long‑term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well‑being program).

Incentive plans, 401(k) plan plus employer contribution and match, Short‑term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non‑qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.