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Quality Assurance Director Jobs in Puerto Rico (NOW HIRING)

Quality Site Head

Aibonito, PR · On-site

$168 - $231/hr

Direct the planning, staffing, development, and budgeting of the site quality organization. * Ensure effective evaluation, management, communication, and documentation of product safety risks.

Specialist QA (5:00 pm - 5:30 am) SUMMARY Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision. FUNCTIONS * Review and ...

Specialist QA (5:00 pm - 5:30 am) SUMMARY Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision. FUNCTIONS - Review and ...

Quality Specialist- 02

Juncos, PR · On-site

$85 - $115/hr

For QA Services in the Drug Substance area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor'sDegree with four(4)years of experiencewithin the pharmaceutical or regulated industry. * Bilingual ...

PR · On-site

The primary purpose of this position is to ensure the quality of product manufactured and also make sure the the Durable & Consumable, commodities and raw materials used in the Drug Product and Drug ...

Showing results 41-60

Quality Assurance Director information

What does a Quality Assurance Director do?

A Quality Assurance Director oversees the development and implementation of quality standards and processes within an organization. They lead teams responsible for inspecting, testing, and ensuring that products or services meet regulatory and company requirements. Their responsibilities also include establishing quality control policies, analyzing data to identify trends or issues, and driving continuous improvement initiatives. In many organizations, they serve as the main liaison between management, production, and regulatory bodies to ensure compliance and customer satisfaction.

What does a Quality Assurance Director do?

As a quality assurance director, you oversee the quality control process at your company and ensure processes and products meet the standards set by organizations like the American Society for Quality (ASQ). In this role, you may help products obtain a quality certification, use statistics to watch for problems with product production lines, and talk with customers to get more information about their experience using the product. Fulfilling the responsibilities and duties of a quality assurance director requires interpersonal skills, leadership skills, a willingness to strive for perfection, and sometimes the ability to work outside of normal hours if the company detects an urgent problem with its products.

What are the key skills and qualifications needed to thrive as a Quality Assurance Director?

To thrive as a Quality Assurance Director, you need expertise in quality management systems, regulatory compliance, and process improvement, often backed by a bachelor’s or master’s degree in a relevant field. Familiarity with tools such as ISO standards, Six Sigma methodologies, and quality management software is crucial. Strong leadership, strategic thinking, and excellent communication skills set top performers apart in this role. These competencies ensure product quality, regulatory adherence, and continuous improvement, directly impacting organizational reputation and operational efficiency.

How does a Quality Assurance Director typically collaborate with cross-functional teams to ensure product quality?

A Quality Assurance Director works closely with departments such as product development, engineering, regulatory affairs, and operations to establish quality standards and processes. They lead regular meetings to align on quality goals, review performance metrics, and address any quality-related issues or risks. This collaborative approach helps to ensure that quality is integrated into every stage of the product lifecycle, from design to delivery. By fostering open communication and teamwork, the director ensures all teams are accountable for maintaining high standards and meeting compliance requirements.

What is the difference between Quality Assurance Director vs Quality Control Manager?

AspectQuality Assurance DirectorQuality Control Manager
CredentialsTypically requires a bachelor’s degree in quality management, engineering, or related field; certifications like ASQ CQE or CQA are commonUsually holds a bachelor’s degree in quality, manufacturing, or engineering; certifications like ASQ CQE are also valued
Work EnvironmentOversees quality assurance processes across departments, focusing on system improvements and complianceManages day-to-day inspection and testing activities to ensure product quality
Industry UsageUsed in manufacturing, software, healthcare, and industries emphasizing process qualityCommonly found in manufacturing, production, and assembly lines

The Quality Assurance Director focuses on establishing and maintaining quality systems and processes, ensuring compliance and continuous improvement. In contrast, the Quality Control Manager concentrates on inspecting products and identifying defects during production. Both roles are essential for quality management but differ in scope and responsibilities.

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

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

What job categories do people searching Quality Assurance Director jobs in Puerto Rico look for?

The top searched job categories for Quality Assurance Director jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Quality Assurance Director jobs?

Cities in Puerto Rico with the most Quality Assurance Director job openings:

Infographic showing various Quality Assurance Director job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Quality Site Head

Baxter Healthcare

Aibonito, PR • On-site

$168 - $231/hr

Other

Medical, Dental, Life, Retirement, PTO

Posted 18 days ago


Job description

This is whereyour work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Your Role

As the Quality Site Head, you will serve as the Quality Management Representative for the plant and provide leadership across all quality functions. You will partner closely with site and business leadership to ensure compliance with applicable regulations and standards, support regulatory inspections, drive quality performance, and strengthen a culture of continuous improvement.

This role offers the opportunity to influence site strategy, lead a high-performing quality organization, and play a critical role in delivering products that improve patient outcomes around the world.

Your Team

Every role within Quality makes a difference. Baxter's products reach patients worldwide. Individuals in Quality either develop new processes or solve new production challenges. They are trusted and encouraged to apply creativity. Your specific role will influence a part of our global operation.

The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always.

What you'll be doing
  • Provide overall leadership and governance for the site Quality Management System (QMS), ensuring requirements are effectively established, maintained, and continuously improved.

  • Serve as the site Quality Management Representative and ensure compliance with applicable regulatory, customer, and Baxter quality requirements.

  • Lead preparations for and management of regulatory inspections and external audits.

  • Establish, communicate, and monitor measurable quality objectives aligned with business and quality priorities.

  • Direct the planning, staffing, development, and budgeting of the site quality organization.

  • Ensure effective evaluation, management, communication, and documentation of product safety risks.

  • Maintain GMP compliance across the site and oversee critical quality systems and processes.

  • Review and approve quality-related procedures, specifications, records, and product disposition decisions.

  • Lead management review activities and provide regular updates to senior leadership regarding quality system performance and improvement opportunities.

What you'll bring
  • Bachelor’s degree in Engineering, Science, or a related technical discipline required, advanced degree is preferred.

  • Minimum of 10 years of experience in Quality, Manufacturing or related functions within the medical device, pharmaceutical or healthcare products industry.

  • At least 7 years of progressive quality leadership experience, ideally within a global organization.

  • Strong knowledge of FDA regulations, Quality Systems, Good manufacturing practices (GMP) and regulatory compliance requirements.

  • Demonstrated success leading quality organizations in complex manufacturing environments.

  • Experience managing multiple priorities, driving results through ambiguity, and influencing cross-functional stakeholders.

  • Strong understanding of manufacturing processes, product configuration, and quality system methodologies.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $168,000-$231,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, commission, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits

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US Benefits at Baxter (except for Puerto Rico)
  • This is where your well-being matters.
  • Baxter offers comprehensive compensation and benefits packages for eligible roles.
  • Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance.
  • Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching.
  • We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave.
  • Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits.
  • Join us and enjoy the competitive compensation and benefits we offer to our employees.
  • For additional information regarding Baxter US Benefits, please speak with your recruiter or visit Benefits | Baxter
Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Know Your Rights: Workplace Discrimination is Illegal

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

PO Box 1389 Road 721 Km 3|Aibonito, PR 00786|United States of America

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