Mechanical Engineering Manager Jobs in Puerto Rico

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The Sr Engineering Manager of Manufacturing Innovation & Technology Strategy, will lead the Humacao site's innovation function and be responsible for defining, governing, and executing a multi-year innovation portfolio aligned with the site's strategic vision and business objectives. This leader will maintain a balanced focus on current operational needs while shaping the manufacturing technologies, capabilities, and talent required to execute the portfolio.
The role serves as the site's technology strategist, identifying emerging manufacturing, automation, digital, sustainability, and Industry 4.0 opportunities that improve quality, reduce cost, enhance efficiency, strengthen regulatory compliance, and support future growth.
The successful candidate will develop and sustain a high-performing technical organization capable of scouting, evaluating, piloting, and implementing advanced manufacturing technologies while building compelling business cases that secure investment and funding for transformational initiatives.

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

• Develop, own, and continuously refresh the site's 5-year Innovation and Technology Roadmap.
• Create and manage a balanced portfolio of innovation initiatives ranging from incremental improvements to transformational technologies.
• Evaluate emerging technologies, trends, and industry best practices to position the site ahead of future manufacturing challenges.
• Develop innovation investments strategies that align with site objectives, operational priorities, and enterprise goals.
• Drive collaboration across Engineering, Operations, Quality, Supply Chain, Finance, and Global Manufacturing Technology teams.
• Develop organizational capabilities in automation, digital manufacturing, AI, advanced analytics, robotics, and emerging manufacturing technologies.
• Foster a culture of innovation, experimentation, continuous learning, and accountability.
• Plans, directs and implements all aspects of the company's design and development of new medical device products or software systems.
• May develop, evaluate, implement and maintain technical quality assurance and control systems or reliability systems and standards pertaining to materials, techniques, or company products.
• Directs the development of new concepts from initial design to market release.
• Manages feasibility studies of the design to determine if capable of functioning as intended.
• Monitors documentation maintenance throughout all phases of research and development.
• Organizes the coordination of activities with outside suppliers and consultants to ensure timely delivery.
• Selects, develops and evaluates personnel to ensure the efficient operation of the function.

Required Knowledge and Experience:Requires broad management knowledge to lead project teams in one department. Typically has mastery level knowledge and skills within a specific technical or professional discipline with broad understanding of other areas within the job function. Requires a Baccalaureate Engineering degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. 214.2(h)( 4)(iii)(A) and minimum of 7 years of relevant experience with 5+ years of managerial experience, or advanced degree with a minimum of 5 years of relevant experience with 5+ years of managerial experience.

Preferred Qualifications

• Bachelor's degree in Engineering, Mechanical Engineering, Manufacturing, Automation, Industrial Engineering, Electrical Engineering, or related field.
• Demonstrated experience leading automation and technology implementation projects.
• Strong financial and business acumen with experience building executive-level business cases.
• Experience managing multi-million-dollar capital portfolios.
• Proven ability to lead cross-functional teams in highly regulated manufacturing environments.
• Lean Six Sigma , DRM or equivalent continuous improvement certification.
• Advanced statistical analysis(DOE, SPC, MSA, process capability studies)
• Equipment qualification & validation leadership(IQ/OQ/PQ)
• Regulatory knowledge(FDA QSR, ISO 13485, GMP)
• Cost reduction and value engineering
• Project management(Agile, PMP fundamentals)

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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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.

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 findhere 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.