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Senior Qa Engineer Jobs in Puerto Rico (NOW HIRING)

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance Engineering Team located in Fajardo, Puerto Rico and will be an on-site role. What you will do: * Provide ...

The Senior QA Supervisor also helps maintain compliance with company policies and regulatory standards while promoting a culture of quality, accountability, and continuous improvement.

QA Specialist- ProQN669

Juncos, PR · On-site

$60 - $80/hr

Bachelor's degree in Science or Engineering with 4 years of directly related experience . Key ... Provide quality and compliance guidance to senior management regarding quality, compliance, supply ...

Showing results 21-40

Senior Qa Engineer information

What is a senior QA engineer?

Senior QA Engineers are experienced professionals responsible for ensuring the quality and reliability of software products. They design and implement test plans, automate testing processes, and identify bugs or issues before software is released. These engineers collaborate closely with development teams, provide mentorship to junior QA staff, and help establish best practices in quality assurance. Their expertise is critical in maintaining high standards and delivering robust products to customers.

What skills and qualifications are needed to be a senior QA engineer?

To thrive as a Senior QA Engineer, you need a deep understanding of software testing methodologies, test automation, and strong analytical skills, typically supported by a degree in computer science or a related field. Proficiency with automation tools like Selenium, JUnit, or TestNG, as well as experience with CI/CD systems and version control (e.g., Git), is highly valued. Strong problem-solving abilities, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and ensuring product quality. These competencies are crucial for identifying defects early, maintaining high software standards, and delivering reliable products in fast-paced development environments.

How does a senior QA engineer collaborate with development and product teams during a project lifecycle?

Senior QA Engineers work closely with both development and product teams throughout all phases of the software development lifecycle. They participate in planning meetings to understand requirements, design test strategies, and identify potential risks early on. During development, they often collaborate with developers to clarify test cases, triage bugs, and ensure quality standards are met. Regular communication with product managers helps ensure that testing aligns with user expectations and business goals. This cross-functional teamwork is essential for delivering high-quality software efficiently.

What is the difference between Senior Qa Engineer vs QA Analyst?

AspectSenior QA EngineerQA Analyst
CredentialsBachelor's in Computer Science or related, experience in QA toolsBachelor's in IT, Computer Science, or related, often with testing certifications
Work EnvironmentInvolved in automation, scripting, and testing strategies within development teamsFocuses on manual testing, test case creation, and defect reporting
Industry UsageCommon in software development, tech companies, and IT servicesUsed across various industries including finance, healthcare, and tech

The main difference is that Senior QA Engineers typically handle automation, scripting, and testing strategy, while QA Analysts focus more on manual testing and test documentation. Both roles require strong testing knowledge, but Senior QA Engineers often have more technical skills and responsibilities in test automation and process improvement.

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

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

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

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

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

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

Infographic showing various Senior Qa Engineer job openings in Puerto Rico as of August 2026, with employment types broken down into 92% Full Time, 4% Part Time, and 4% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Sr Quality Engineer-New Product Introduction

Medtronic

Juncos, PR • On-site

$86K - $116K/yr

Full-time

Posted 4 days ago


Medtronic rating

7.9

Company rating: 7.9 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

155th of 546 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 LifeThe Senior Quality Engineer provides quality leadership and oversight for new product introduction activities, ensuring products and manufacturing processes meet regulatory, quality, and business requirements. This role partners with cross-functional teams to drive risk management, design and process validation, change control, and product transfer activities from development through commercial launch, while supporting continuous improvement and risk burndown initiatives at the site. This role also provides oversight to equipment and process validation activities at the site.
The Senior Quality Engineer is responsible for supporting product and process quality within a regulated manufacturing environment. This role collaborates across functions to establish quality standards, lead quality improvement initiatives, analyze quality data, and ensure compliance with applicable regulations and quality system requirements while driving continuous improvement and operational excellence.
Primary Responsibilities
  • Lead and support continuous improvement projects and quality initiatives that enhance product quality, process performance, and compliance.
  • Develop, implement, maintain, and improve quality standards and protocols for materials, components, and finished products.
  • Partner with engineering and manufacturing teams to ensure quality requirements are effectively integrated into manufacturing processes and operations.
  • Design and implement inspection, testing, and evaluation methods to verify product quality, equipment performance, and process effectiveness.
  • Conduct statistical analysis and quality assurance activities to evaluate product and process performance, identify trends, and support data-driven decision making.
  • Investigate nonconforming products or materials, determine root causes, and ensure appropriate corrective actions are implemented and documented.
  • Ensure quality documentation, corrective actions, and quality system activities comply with applicable regulatory and internal requirements.
  • Provide technical quality support across design, incoming materials, production control, product evaluation, reliability, inventory control, research and development, or other quality-related areas as needed.
Required Qualifications
  • Bachelor's Degree in Engineering and a minimum of 4 years of relevant experience; OR Master's Degree and a minimum of 2 years of relevant experience; OR PhD.
  • Experience supporting quality engineering activities within a regulated manufacturing or medical device environment.
  • Experience applying quality tools and methodologies to support investigations, corrective actions, and process improvements.
  • Experience collaborating with cross-functional teams including engineering, manufacturing, and quality organizations.
Preferred Qualifications
  • Experience with Design Controls, Risk Management, and quality engineering activities throughout the product lifecycle.
  • Experience leading cross-functional projects and influencing stakeholders in a matrixed environment.
  • Expertise with statistical analysis tools including Minitab, Statistical Process Control (SPC), and trend analysis.
  • Lean Six Sigma Green Belt or Black Belt certification.
  • Experience with validation lifecycle management, change control, quality risk management, reliability engineering, product performance testing, and mentoring engineers or project teams.

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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