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Senior Quality Engineer Jobs in Puerto Rico (NOW HIRING)

Sr Quality Engineer

Humacao, PR

$89K - $121K/yr

The Senior Quality Engineer provides quality engineering leadership for machining and selected secondary operations, including anodizing and final pack. This role ensures product and process quality ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

The Senior Quality Engineer provides quality engineering leadership for machining and selected secondary operations, including anodizing and final pack. This role ensures product and process quality ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

The Senior Quality Engineer provides quality engineering leadership for machining and selected secondary operations, including anodizing and final pack. This role ensures product and process quality ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

The Sr. Quality Engineer supports quality assurance activities within a regulated manufacturing environment, ensuring products and processes meet applicable quality, regulatory, and business ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

The Sr. Quality Engineer supports quality assurance activities within a regulated manufacturing environment, ensuring products and processes meet applicable quality, regulatory, and business ...

Sr Quality Engineer

Humacao, PR · On-site +1

$89K - $121K/yr

Collaborates with engineering and manufacturing functions to ensure quality standards are in place ... Communicates with senior internal and external customers and vendors. Exchange information of facts ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

The Sr. Quality Engineer supports quality assurance activities within a regulated manufacturing environment, ensuring products and processes meet applicable quality, regulatory, and business ...

Sr Quality Engineer

Humacao, PR

$89K - $121K/yr

Collaborates with engineering and manufacturing functions to ensure quality standards are in place ... Communicates with senior internal and external customers and vendors. Exchange information of facts ...

Sr. Quality Engineer

Humacao, PR · On-site

$89K - $120K/yr

Collaborates with engineering and manufacturing functions to ensure quality standards are in place. * Devises and implements methods and procedures for inspecting, testing, and evaluating the ...

Sr Quality Engineer

Juncos, PR · On-site +1

$86K - $116K/yr

... product quality. Develops manufacturing processes that are applicable to statistical process ... Provides guidance to engineering regarding design concepts and specification requirements to best ...

Sr. Quality Engineer

Juncos, PR · On-site

$86K - $117K/yr

Collaborates with engineering and manufacturing functions to ensure quality standards are in place. * Devises and implements methods and procedures for inspecting, testing, and evaluating the ...

Quality Senior Engineer

Arecibo, PR · On-site

$76K - $103K/yr

The Senior Quality Engineer works closely with Operations, other cross-functional team members and suppliers to ensure stable processes, robust control plans, and reliable product/components ...

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Showing results 1-20

Senior Quality Engineer information

What is a senior quality engineer?

A Senior Quality Engineer is responsible for testing the functionality of technical components or products for their company. As a quality engineer, your job duties include developing testing scripts, performing functional testing as part of the development team, and documenting any defects that you discover. The qualifications needed for a career as a senior quality engineer include a bachelor’s degree in quality, mechanical, or industrial engineering and as many as seven years of experience. Some employers may prefer a master’s degree. You also need solid analytical skills and experience testing a variety of complex technical components or products.

What are the key skills and qualifications needed to thrive as a senior quality engineer, and why are they important?

To thrive as a Senior Quality Engineer, you need expertise in quality assurance methodologies, root cause analysis, and a relevant engineering degree or certification such as Six Sigma. Familiarity with quality management systems (QMS), statistical process control tools, and software like Minitab or SAP is typically expected. Strong analytical thinking, leadership, and effective communication skills help drive continuous improvement and cross-functional collaboration. These competencies ensure product reliability, regulatory compliance, and sustained operational excellence.

How does a senior quality engineer typically collaborate with cross-functional teams during product development?

Senior Quality Engineers play a vital role in cross-functional collaboration by acting as a bridge between engineering, manufacturing, and product management teams. They are often involved in design reviews, risk assessments, and root cause analysis meetings to ensure quality is built into every stage of development. Effective communication and problem-solving skills are essential, as Senior Quality Engineers must provide feedback, share best practices, and advocate for quality standards while balancing project timelines. This collaborative environment enables them to influence product outcomes and drive continuous improvement initiatives.

What is the difference between Senior Quality Engineer vs Quality Assurance Manager?

AspectSenior Quality EngineerQuality Assurance Manager
ResponsibilitiesDesigns and implements testing processes, analyzes quality data, supports product developmentOversees QA teams, develops quality policies, manages quality assurance projects
Required SkillsTechnical testing, problem-solving, data analysisLeadership, project management, communication
CertificationsASQ Certified Quality Engineer (CQE), Six SigmaASQ CQE, Six Sigma, management certifications
Work EnvironmentEngineering teams, product developmentQA teams, cross-departmental collaboration

While both roles focus on quality, Senior Quality Engineers primarily handle technical testing and process improvements, whereas Quality Assurance Managers oversee QA teams and develop quality strategies. The roles often overlap but differ in scope and leadership responsibilities.

How much does a senior quality engineer earn?

A senior quality engineer typically earns between $80,000 and $120,000 annually, depending on experience, industry, and location. They often have certifications like Six Sigma or ISO auditor training and work in manufacturing, technology, or healthcare sectors.

What are the most commonly searched types of Quality Engineer jobs in Puerto Rico?

The most popular types of Quality Engineer jobs in Puerto Rico are:

What are popular job titles related to Senior Quality Engineer jobs in Puerto Rico?

For Senior Quality Engineer jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Senior Quality Engineer jobs in Puerto Rico look for?

The top searched job categories for Senior Quality Engineer jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Senior Quality Engineer jobs?

Cities in Puerto Rico with the most Senior Quality Engineer job openings:

Infographic showing various Senior Quality Engineer job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, 2% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

$89K - $121K/yr

Full-time

Re-posted 22 days ago


Medtronic rating

7.8

Company rating: 7.8 out of 10

Based on 177 frontline employees who took The Breakroom Quiz

178th of 540 rated manufacturers


Job description

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 LifeA career at Medtronic is like no other. We're purposeful. We're committed. And we're driven by our Mission to alleviate pain, restore health and extend life for millions of people worldwide.
The Senior Quality Engineer provides quality engineering leadership for machining and selected secondary operations, including anodizing and final pack. This role ensures product and process quality by partnering with cross-functional teams to confirm that manufacturing processes, equipment, components, and documentation meet regulatory requirements, and Medtronic Quality Management System expectations.
The role drives compliance with GMP, FDA, and ISO requirements through disciplined documentation, traceability, investigation support, and audit readiness. The Senior Quality Engineer also strengthens product and process robustness by analyzing data, identifying quality risks, supporting nonconformance and CAPA activities, and collaborating with Manufacturing, Engineering, Supply Chain, and Quality partners to enable successful product launch and sustained

A Day in the Life

Partner with Manufacturing, Process Development, and Engineering teams to define, implement, and sustain effective quality controls for machining and secondary manufacturing processes.

Develop and implement inspection, testing, validation, and process evaluation methods to ensure equipment, components, and products consistently meet established requirements.

Apply statistical analysis and quality engineering tools to evaluate process capability, supportcomponentand process qualification, and investigate products, materials, or processes that do not meet specifications.

Ensure investigations, corrective actions, validations, and supporting documentation are compliant, technically justified, risk-based, and inspection-ready.

Lead or support product lifecycle quality activities, including process quality, incoming materials, product evaluation, validation, change management, and continuous improvement.

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

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

Required Knowledge and Experience: Requires a Bachelor's degreeand minimum of 4 years of relevant experience OR Master's degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience.

Engineering Degree required

Must Have:MinimumRequirements

  • Education:Bachelor's degree in engineeringrequired.

  • Experience:Minimum of 4 years of relevant engineering, quality, or manufacturing experience required; or amaster's degree in engineeringwith a minimum of 2 years of relevant experience.

  • Regulated manufacturing:Experience working in a regulated manufacturing environment, preferably medical devices, pharmaceutical, or other highly controlledindustry.

  • Quality systems:Working knowledge of quality system expectations, including documentation, nonconformance handling, corrective and preventive actions, change control, and audit readiness.

  • Technical execution:Ability to support manufacturing process quality activities, investigations,validationdeliverables, risk assessments, and product/process performance monitoring.

Nice to Have

  • Education discipline:Preferredbachelor's ormaster's degree in Mechanical, Industrial, Electricalengineering.

  • Medical device experience:Experience in medical device or other FDA/ISO-regulated manufacturing environment, including GMP expectations and inspection readiness.

  • Quality systems:Practical knowledge of ISO 13485, FDA Quality System Regulation expectations, nonconformance management, CAPA, document control, change control, and risk management.

  • Validation:Knowledge of equipment, process, product, and software validation concepts, including URS, SRS, IQ, OQ, PQ, risk-based validation, andimplementationreadiness.

  • Manufacturing process knowledge:Experience supporting machining, anodizing, final pack, inspection, test methods,componentqualification, or other manufacturing process controls.

  • Problem solving and risk:Experience applying root cause analysis and risk assessment tools such as 5 Whys, Fishbone, FMEA, fault tree analysis, or similar structured methods.

  • Data and statistics:Experience using SPC, capability analysis, DOE, trending, sampling rationale, or statistical methods to support investigations, process monitoring, and continuous improvement.

  • Digital tools:Hands-on experience with Minitab, JMP, Excel advanced functions, Power BI, PowerPoint, SAP, JDE, Factory Works, or similar systems used for data analysis, reporting, traceability, and manufacturing execution.

  • Continuous improvement:Lean Six Sigma Green Belt, Black Belt, or equivalent training/certification preferred.

  • Technical writing:Demonstratedability to write clear, technically sound, and audit-ready protocols, reports, investigations, justifications, and quality documentation.

  • Leadership and collaboration:Strong critical thinking, communication, prioritization, and cross-functional collaboration skills in a fast-paced manufacturing environment.

  • Automation and AI enablement:Experience with data extraction, automation, dashboards, or basic programming tools such as VBA, Python, Copilot, ChatGPT, Gemini, or similar applications to improve reporting and process analysis.

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.

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 AskHR@medtronic.com.

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).

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 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.


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