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Qa Associate Jobs in Puerto Rico (NOW HIRING)

Position Summary The QA Specialist is responsible for ensuring product quality, process compliance, and continuous improvement within manufacturing or service delivery operations. This role combines ...

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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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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Sr. Quality Assurance Specialist

San Juan, PR · On-site

$60K - $75K/yr

  • Medical

  • PTO

We are looking candidates with experience within regulated environment for a SR. Quality Assurance Specialist in Hato Rey, Puerto Rico. Requirement: * Bachelor's degree in Engineering in Engineering ...

PR · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ensures quality control and quality assurance compliance across the manufacturing site. Serves as an integral member of site leadership team with a focus on ensuring quality system requirements are ...

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 ...

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Qa Associate information

What is a QA associate?

QA Associates, or Quality Assurance Associates, are professionals responsible for monitoring, inspecting, and proposing measures to improve processes that ensure the quality of products or services in a company. They work closely with production, development, and compliance teams to make sure that products meet required standards and regulations. Their tasks often include reviewing documentation, conducting audits, and reporting on quality metrics. QA Associates play a crucial role in maintaining customer satisfaction and regulatory compliance in industries such as pharmaceuticals, manufacturing, and software.

What are the key skills and qualifications needed to thrive as a QA associate?

To thrive as a QA Associate, you need a solid understanding of quality assurance methodologies, attention to detail, and often a degree in a scientific or technical field. Familiarity with tools like LIMS, GMP/GLP regulations, and quality management systems, as well as relevant certifications such as ASQ or Six Sigma, is typically required. Strong analytical thinking, effective communication, and problem-solving abilities help you excel within cross-functional teams. These skills ensure product compliance, support continuous improvement, and maintain high standards in regulated environments.

What are some common challenges faced by a QA associate, and how can they be addressed?

QA Associates often encounter challenges such as managing tight deadlines, adapting to rapidly changing project requirements, and ensuring thorough test coverage. Effective communication with developers and other team members is crucial to address issues quickly and maintain product quality. Staying organized, using test management tools, and participating in regular stand-up meetings can help QA Associates stay on top of their workload and deliver consistent results.

Is a QA associate a difficult job?

A QA associate role involves testing products or software to identify defects, which requires attention to detail, analytical skills, and knowledge of testing tools. The job can be challenging depending on project complexity and deadlines but is generally manageable with proper training and experience.

Is a QA associate a good entry level job?

A QA associate position is often suitable for entry-level candidates, as it typically requires basic knowledge of testing processes, attention to detail, and familiarity with tools like test management software. It provides a foundation in quality assurance practices and can lead to more advanced roles in software testing or quality management.

What does a QA associate do?

A QA associate is responsible for testing products, software, or processes to ensure they meet quality standards and specifications. They develop test plans, identify defects, document issues, and work with teams to improve quality, often using testing tools and following industry protocols.

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

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

Infographic showing various Qa Associate job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 2% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Quality - Quality Assurance Inspector I

medplast

Vega Baja, PR

Full-time

Re-posted 3 days ago


Job description

Quality Assurance Inspector I

Position Description/Responsibilities:

The Quality Assurance Inspector l is responsible to provide general quality assurance support in the areas of inspection manufacturing and assembly. Performs mechanical, electrical and visual inspection of manufactured product and/or processes per documentation (drawings, specifications and procedures) and industry standards. Freedom to act, under supervision, in semi-structured assignments that requires adherence to defined procedures and/or specific, detailed instructions with limited originality, Solves problems of limited scope and com complexity. Demonstrates Viant values.

Position Authority:

This position has the authority to accept or reject materials, subassemblies, assemblies and processes that affect the quality and safety of products. This includes the authority to stop production if necessary to assure that nonconforming products are not released for distribution.

Essential Functions:

  • Follows all Good Manufacturing Practices and SOP’s as defined by Viant’s policies, practices and procedures to ensure that FDA regulations, GMP, ISO13485, and Viant quality standards are met.
  • Checks material disposition and identification in order to meet GMP regulations.
  • Inspect and document in-bound raw materials for conformance.
  • Collects samples at scheduled intervals from each machine.
  • Perform in process dimensional and visual inspection to assure compliance with customer specification giving appropriate disposition according to Viant’s procedures.
  • Responsible for documentation of (in-process) sampling plan, disposition and inspection results
  • Perform basic ERP transactions.
  • Work on validation projects as needed.
  • Manage retains of production and validation projects.
  • Audits assigned areas.
  • Verifies that the process inspections and areas in charge are in conformance with Viant’s procedures.

Skills:

  • Proficient in knowledge of a variety of testing equipment (pin gauges, snap gauges, micrometer, caliper, etc.).
  • Ability to interpret component specifications, drawings and quality procedures.
  • Proficient technical writing skills and use of documentation programs (e.g., Office Windows, Excel, Access, PowerPoint, etc.)
  • Performs basic arithmetic calculations: add, multiply, subtract, and divide in all units of measure using whole numbers, common fractions and decimals.
  • Requires the ability to adjust a microscope e lens to bring an object into sharp focus.

Physical Requirements:

  • Light physical activity performing non-strenuous, day-to-day activities of a primarily productive nature.
  • Moderate lifting (20 lbs.), carrying (10 lbs.), bending, and prolonged sitting.
  • Manual dexterity sufficient to reach/handle items, work with fingers, and perceive attributes of objects and material. Intensive handwork.
  • Requires the ability to identify and distinguish colors and shapes.
  • Well-lighted, air-conditioned, indoor production setting with adequate ventilation.

Equipment Used:

  • Mechanical and electrical teste equipment, calipers, gauges, and standard office computer.
  • Utilize tools, gauges and other inspection equipment to obtain product specification data.

Qualifications:

  • Associates degree or equivalent in work experience. Bachelor Degree in Natural Sciences preferable. English understanding, quality oriented and statistical knowledge.
  • 3 months to 1 year of recent experience in medical device industry, with experience of different medical products with as molding operator.