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Quality Associate Jobs in Puerto Rico (NOW HIRING)

BioPharma Consulting JAD Group

Specialist QA

Juncos, PR · On-site

The Specialist QA performs a broad range of Quality Assurance activities under minimal supervision ... Associate's + 8 years of directly related experience OR * High School/GED + 10 years of directly ...

ABB

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

Quality & CI Manager At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what you ...

trane technologies

Quality Engineer

Arecibo, PR

$62K - $80K/yr

Experience collaborating with Suppliers to ensure part and component quality. Where is the work: Arecibo Facility, Puerto Rico What you will do: * Leads and participates actively in identifying and ...

Kelly Services

Quality Inspector I

Santa Isabel, PR · On-site

Kelly ® Engineering is seeking Quality Inspector I for contract position at manufacturing client ... Associate or Technical Degree preferred Minimum 1 year experience in a manufacturing environment.

Trane Technologies plc

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

Experience collaborating with Suppliers to ensure part and component quality. Where is the work: Arecibo Facility, Puerto Rico What you will do: * Leads and participates actively in identifying and ...

Trane Technologies plc

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

Experience collaborating with Suppliers to ensure part and component quality. Where is the work: Arecibo Facility, Puerto Rico What you will do: * Leads and participates actively in identifying and ...

Jj

Quality Assurance Technician

San Lorenzo, PR · On-site

Quality Control Job Category: Business Enablement/Support All Job Posting Locations: San Lorenzo ... Support associates on defect awareness and specifications requirements. Qualifications ...

BlackBerry Inc.

Customer Quality Engineer

Arecibo, PR · On-site

$125 - $150/hr

Quality & CI Manager__At ABB, we help industries outrun - leaner and cleaner. Here, progress is an ... Will considered associate's degree in Eng or related field with 10+ years relevant work ...

ProSolar

Quality Assurance

Carolina, PR · On-site

$60 - $80/hr

Quality Assurance Specialist en Prosolar es responsable de garantizar que todos los procesos, instalaciones y proyectos solares cumplan con los más altos estándares de calidad, seguridad y ...

ProSolar Florida

Quality Assurance

Carolina, PR · On-site

$60 - $80/hr

Quality Assurance Specialist en Prosolar es responsable de garantizar que todos los procesos, instalaciones y proyectos solares cumplan con los más altos estándares de calidad, seguridad y ...

FITS LLC

Quality Engineer II

Humacao, PR · On-site

$72K - $93K/yr

Experience with quality and business systems The Personality Part: * Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other ...

FITS LLC

Quality Engineer II

Humacao, PR · On-site

$60 - $80/hr

Experience with quality and businesssystems The Personality Part: * Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other ...

Medtronic

Quality Engineer I -

Juncos, PR · On-site

$70K - $90K/yr

The Quality Engineer I supports in quality and supplier engineering activities associated with product, process maintenance, equipment including evaluation and implementation of changes to materials ...

Medtronic

Quality Engineer I -

Juncos, PR · On-site

$70K - $90K/yr

The Quality Engineer I supports in quality and supplier engineering activities associated with product, process maintenance, equipment including evaluation and implementation of changes to materials ...

FITS LLC

Quality, Lead Investigator

Manati, PR · On-site

For Compliance services in the Quality area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's Degree in Chemical Engineering, Biology, or Microbiology Science & five (5) years of experience in ...

Medtronic

Quality Engineer I -

Juncos, PR · On-site

$70K - $90K/yr

The Quality Engineer I supports in quality and supplier engineering activities associated with product, process maintenance, equipment including evaluation and implementation of changes to materials ...

CERES

PR

$22 - $27/hr

Quality Control Inspector (Construction) Location: Puerto Rico Reports to: Project Manager or ... Preferred Qualifications Associate's Degree or Bachelor's Degree in engineering, construction ...

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Quality Associate information

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

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

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

More about Quality Associate jobs

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

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

What cities in Puerto Rico are hiring for Quality Associate jobs?

Cities in Puerto Rico with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate 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.

Specialist QA

Juncos, PR • On-site

BioPharma Consulting JAD Group
Biotechnology Research and Development • 51 - 200 employees
Learn more about BioPharma Consulting JAD Groupexternal

Full-time

This job post has expired today. Applications are no longer accepted.

Key responsibilities

  • Review and approve product manufacturing reports, process validation protocols, and batch records.

  • Perform on-the-floor quality assurance reviews, approvals, and tracking of cGMP processes, deviations, CAPAs, and validations.

  • Support investigations, audits, and internal/external inspections related to quality and compliance.

Job description

The Specialist QA performs a broad range of Quality Assurance activities under minimal supervision, ensuring compliance with cGMP requirements, internal procedures, and regulatory expectations. This role provides on‑the‑floor oversight, documentation review, quality system support, and cross‑functional collaboration to maintain product quality and operational excellence.

FUNCTIONS

  • Review and approve product MPs, process validation protocols, and manufacturing reports.
  • Perform on‑the‑floor Plant Quality Assurance (PQA) review, approval, and tracking of cGMP processes, batch records, MES/EBR, SAP, EDMQ, DQMS, Trackwise documentation, deviations, CAPAs, and validations.
  • Participate in incident triage teams and ensure deviation initiation, documentation, and procedural compliance.
  • Approve Environmental Characterization reports and release sanitary utility systems.
  • Approve planned incidents, NC investigations, CAPA records, and change controls.
  • Lead investigations, audits, and support internal/external inspections as part of the audit management team.
  • Represent QA in New Product Introduction (NPI) activities and provide quality oversight for new products.
  • Own and maintain site quality program procedures; act as designee for QA leadership on CCRB.
  • Review risk assessments and support automation, facilities, environmental, and engineering programs.
  • Review and approve Work Orders and EMS/BMS alarms.
  • Provide lot disposition and authorize lots for shipment.
  • Ensure production records and testing results are complete, accurate, and compliant with cGMP.
  • Coordinate testing with contract laboratories and vendors; review external lab data for accuracy and compliance.
  • Support commissioning, qualification, and validation activities (IQ/OQ/PQ, Validation Master Plans, protocols, test scripts, summary reports).
  • Serve as a strategic advisor regarding quality, compliance, supply, and safety risks.
  • Champion continuous improvement initiatives, programs, and projects.
  • Maintain adherence to assigned training requirements.
  • Collaborate cross‑functionally with Manufacturing, Process Development, Validation, QC, Warehouse, Engineering, Facilities, Environmental, Contractors, and other stakeholders.

Requirements

EDUCATION

  • Doctorate OR
  • Master’s + 2 years of directly related experience OR
  • Bachelor’s + 4 years of directly related experience OR
  • Associate’s + 8 years of directly related experience OR
  • High School/GED + 10 years of directly related experience.

PREFERRED QUALIFICATIONS

  • Experience in Change Control, Documentation Review, Validation, PPQ.
  • Demonstrated expertise in Quality Systems (deviations, CAPA, change control).
  • Experience with computer systems validation or computer systems QA (medical device or consulting background preferred).
  • Strong knowledge of manufacturing, distribution, QA, QAL, and Process Development processes.
  • Experience with GxP application validation and compliance documentation.
  • Proven ability to lead, influence, and negotiate across teams.
  • Strong organizational skills and ability to follow assignments through to completion.
  • Ability to interact effectively with regulatory agencies.
  • Strong communication skills in English and Spanish (written and oral).
  • Advanced data trending, evaluation, and compliance assessment skills.
  • Ability to work independently and interact effectively at all organizational levels.

Benefits

  • Administrative shift.
  • 6‑month contract with possible extension.