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.
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.
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.
Aibonito, PR · On-site
$168K - $231K/yr
Direct the planning, staffing, development, and budgeting of the site quality organization. * Ensure effective evaluation, management, communication, and documentation of product safety risks.
Aibonito, PR · On-site
$168K - $231K/yr
Direct the planning, staffing, development, and budgeting of the site quality organization. * Ensure effective evaluation, management, communication, and documentation of product safety risks.
Carolina, PR · On-site
$50 - $80/hr
Support QA oversight of Site Utilities Systems and Environmental Monitoring results. * Coordinate with impacted areas including the laboratory, utilities, and manufacturing operations. * Ensure ...
Carolina, PR · On-site
$50 - $80/hr
Support QA oversight of Site Utilities Systems and Environmental Monitoring results. * Coordinate with impacted areas including the laboratory, utilities, and manufacturing operations. * Ensure ...
Carolina, PR · On-site
$60 - $80/hr
Support QA oversight of Site Utilities Systems and Environmental Monitoring results. * Coordinate with impacted areas including the laboratory, utilities, and manufacturing operations. * Ensure ...
Carolina, PR · On-site
$60 - $80/hr
Support QA oversight of Site Utilities Systems and Environmental Monitoring results. * Coordinate with impacted areas including the laboratory, utilities, and manufacturing operations. * Ensure ...
The Manager, Infrastructure & Workplace Services will lead a team of QA Analysts, testers and a technical writer to support the Data Labeling and Compliance Team. The Manager will be responsible for ...
The Manager, Infrastructure & Workplace Services will lead a team of QA Analysts, testers and a technical writer to support the Data Labeling and Compliance Team. The Manager will be responsible for ...
Juncos, PR · On-site
$70 - $90/hr
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 ...
Juncos, PR · On-site
$70 - $90/hr
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 ...
The Manager, Infrastructure & Workplace Services will lead a team of QA Analysts, testers and a technical writer to support the Data Labeling and Compliance Team. The Manager will be responsible for ...
The Manager, Infrastructure & Workplace Services will lead a team of QA Analysts, testers and a technical writer to support the Data Labeling and Compliance Team. The Manager will be responsible for ...
The Manager, Infrastructure & Workplace Services will lead a team of QA Analysts, testers and a technical writer to support the Data Labeling and Compliance Team. The Manager will be responsible for ...
The Manager, Infrastructure & Workplace Services will lead a team of QA Analysts, testers and a technical writer to support the Data Labeling and Compliance Team. The Manager will be responsible for ...
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 ...
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 ...
Juncos, PR · On-site
$150 - $190/hr
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
Juncos, PR · On-site
$150 - $190/hr
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
Adhere to relevant quality assurance standards and regulations * Continuously improve the testing process as services, standards, and requirements evolve * Leverage testing software such as Jira or ...
Adhere to relevant quality assurance standards and regulations * Continuously improve the testing process as services, standards, and requirements evolve * Leverage testing software such as Jira or ...
Adhere to relevant quality assurance standards and regulations * Continuously improve the testing process as services, standards, and requirements evolve * Leverage testing software such as Jira or ...
Adhere to relevant quality assurance standards and regulations * Continuously improve the testing process as services, standards, and requirements evolve * Leverage testing software such as Jira or ...
Adhere to relevant quality assurance standards and regulations * Continuously improve the testing process as services, standards, and requirements evolve * Leverage testing software such as Jira or ...
Adhere to relevant quality assurance standards and regulations * Continuously improve the testing process as services, standards, and requirements evolve * Leverage testing software such as Jira or ...
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
Juncos, PR · On-site
$130 - $170/hr
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
Juncos, PR · On-site
$130 - $170/hr
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
... directing the allocation of resources. Your managerial experience may run concurrently with the ... Quality Assurance, Quality Systems, Manufacturing, or Compliance within the pharmaceutical ...
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 ...
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 ...
Barceloneta, PR · On-site
$12 - $13.09/hr
The primary purpose of this position is to ensure the quality of the pharmaceutical product (Drug Product) and the manufacturing process. Also, to make sure raw materials and commodities used are of ...
Barceloneta, PR · On-site
$12 - $13.09/hr
The primary purpose of this position is to ensure the quality of the pharmaceutical product (Drug Product) and the manufacturing process. Also, to make sure raw materials and commodities used are of ...
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.
| Aspect | Quality Assurance Director | Quality Control Manager |
|---|---|---|
| Credentials | Typically requires a bachelor’s degree in quality management, engineering, or related field; certifications like ASQ CQE or CQA are common | Usually holds a bachelor’s degree in quality, manufacturing, or engineering; certifications like ASQ CQE are also valued |
| Work Environment | Oversees quality assurance processes across departments, focusing on system improvements and compliance | Manages day-to-day inspection and testing activities to ensure product quality |
| Industry Usage | Used in manufacturing, software, healthcare, and industries emphasizing process quality | Commonly 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.
The most popular types of Quality Assurance jobs in Puerto Rico are:
The top searched job categories for Quality Assurance Director jobs in Puerto Rico are:
Cities in Puerto Rico with the most Quality Assurance Director job openings:

$168 - $231/hr
Other
Medical, Dental, Life, Retirement, PTO
Posted 18 days ago
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 RoleAs 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 TeamEvery 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 doingProvide 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.
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)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 AccommodationsBaxter 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