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A Day in the Life

The Cranial & Spine Manufacturing Engineering function in Humacao, Puerto Rico supports the development, implementation, and improvement of manufacturing processes, equipment, tooling, and production methods that enable successful new product introduction and transfer of product and technology designs into manufacturing. The Manufacturing Engineer II partners with R&D, engineering, quality, and manufacturing teams to support new technologies and therapies from concept through launch, while maintaining product quality and regulatory compliance.

This position is onsite in Humacao, Puerto Rico and requires less than 10% travel.

The Manufacturing Engineer II is an experienced individual contributor responsible for developing, implementing, and improving manufacturing processes, equipment, tooling, and production solutions in support of Cranial & Spine new product introduction and R&D initiatives. This role works independently on moderately complex projects, contributes to design transfer and launch readiness, recommends process improvements, and provides technical guidance to entry-level team members as needed.

         

         

Responsibilities may include the following and other duties may be assigned.

• Design and implement manufacturing processes, procedures, equipment, tooling, and production layouts for new products, existing products, and design transfer activities.
• Develop manufacturing solutions supporting R&D projects, new technologies, product designs, and transfer to manufacturing.
• Define sequences of operations and fabrication requirements for tooling and equipment to support product performance, manufacturability, and production readiness.
• Evaluate machinery, equipment, and tooling performance; investigate deficiencies; and implement corrective actions to support product quality and operational efficiency.
• Develop and improve manufacturing processes using Statistical Process Control (SPC), process capability methods, and other process control techniques.
• Incorporate inspection, testing, validation, and manufacturing requirements into production processes and plans.
• Partner with R&D and cross-functional engineering teams to provide input on design concepts, specifications, equipment selection, and manufacturing methods.
• Recommend process, equipment, and system improvements while ensuring manufacturing processes and procedures comply with applicable regulatory requirements.
• Support design transfer, process validation, and launch readiness activities for new products and technologies.
• Provide technical guidance and support to entry-level engineers and cross-functional partners as needed.

Required Qualifications

• Bachelor’s degree in Engineering with 2+ years of relevant experience, or Master’s degree in Engineering with 0+ years of relevant experience.

Preferred Qualifications

• Experience in manufacturing process development, equipment, tooling, or new product introduction.
• Experience with Statistical Process Control (SPC), process capability, and manufacturing data analysis.
• Experience with Design for Manufacturing (DFM), process validation, or design transfer.
• Experience with Computer-Aided Design (CAD), Lean Manufacturing, or continuous improvement practices.
• Experience in medical device or other regulated manufacturing environments.
  

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.

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Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind: 

Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. 

Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. 

If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. 

If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected]. 

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Benefits & Compensation
 

Medtronic offers a competitive Salary and flexible Benefits Package
A 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.
 

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This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

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.