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Manual Qa Tester 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 ... Coordinate testing with contract laboratories and vendors; review external lab data for accuracy ...

INVID

QA Automation II

San Juan, PR · On-site

$80 - $100/hr

As a mid‑level automation specialist, you will collaborate closely with developers, product owners, and QA teammates to drive best practices, improve testing efficiency, and contribute to ...

ADP, Inc.

QA Specialist

Aguadilla, PR · On-site

$60 - $80/hr

Perform electrical and visual testing of solar modules. * Monitor Production processes to ensure ... Implement and maintain QA QC procedures and protocols. * SCAR (Supplier Corrective Action Request)

New

CEGSoft

Quality Assurance Engineer

San Juan, PR · On-site

$45K - $52K/yr

We are looking for a Quality Assurance Engineer to help us validate, test, and continuously improve ... Design and perform functional, exploratory, smoke, regression, end-to-end, and release testing ...

Frey Consulting Group

QA Specialist- ProQN669

Juncos, PR · On-site

$60 - $80/hr

Perform on-the-floor Plant Quality Assurance (PQA) review, approval, and tracking of cGMP processes, procedures, testing methods, manufacturing documentation, records, and batch records. * Work with ...

Inteldot

Specialist QA 35669

Juncos, PR · On-site

Perform On-the-floor Plant Quality Assurance (PQA) review, approval, and tracking of cGMP processes, procedures, testing methods in manufacturing, documents and records, batch record review, MES, EBR ...

JLL

QA Specialist

Gurabo, PR · On-site

Position Summary The QA Specialist is responsible for ensuring product quality, process compliance ... Inspection & Testing * Conducts in-process inspections and final product inspections according to ...

Jj

Quality Assurance Technician

San Lorenzo, PR · On-site

Conducts routine physical inspection, testing, or evaluation to ensure quality of products ... Delivers samples to Finished Goods QA Lab if needed. * Performs data analysis and executes final ...

Jj

QA Auditor - Parenterals

Gurabo, PR · On-site

Quality Assurance Job Category: Professional All Job Posting Locations: Gurabo, Puerto Rico, United ... testing and inspection of materials and products. * Review batch records, in-process documents ...

Johnson and Johnson

QA Auditor - Parenterals

Gurabo, PR · On-site

Quality Assurance Job Category: Professional All Job Posting Locations: Gurabo, Puerto Rico, United ... testing and inspection of materials and products. * Review batch records, in-process documents ...

Grupo Triple-S

IT QA Analyst

Guaynabo, PR · On-site

IT QA Analyst Company: Triple-S Management Ubicaciones de puesto (breve): Guaynabo, PR Fecha de ... Conduct manual regression, integration, and end-to-end testing for new and existing functionality ...

Mirus Consulting Group

Specialist QA - 35615

Juncos, PR · On-site

$65 - $95/hr

Position Summary The Specialist QA is responsible for ensuring compliance with quality standards ... Experience with IQ/OQ/PQ execution and Functional Testing. * Knowledge of Process Validation and ...

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Manual Qa Tester information

What is a manual QA tester?

As a Manual QA Tester, your responsibilities and duties include the manual testing of new software in both the pre- and post-release stage of the development lifecycle. You look for problems and bugs in the system that users may encounter and help developers find solutions to the issues. You may work as a black box tester, which means you do not know the code or workings of the system and test, experiencing the system as a user. You may also work as a clear or white box tester, where you have access and knowledge about the code and workings of the system and can exam each test case with both the user’s and developer’s perspective in mind.

What does a manual QA tester do?

A Manual QA Tester is responsible for manually testing software applications to ensure they function correctly and meet specified requirements. They create and execute test cases, identify bugs or issues, and report their findings to the development team for resolution. Unlike automated testers, manual QA testers perform testing activities without using scripts or automation tools, relying instead on their understanding of the software and user experience. Their work is crucial to delivering high-quality, user-friendly products.

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

To thrive as a Manual QA Tester, you need a strong attention to detail, analytical thinking, and a solid understanding of software development and testing methodologies, often supported by a relevant degree or experience in quality assurance. Familiarity with bug tracking tools (like JIRA), test case management systems, and basic SQL is typically required. Excellent communication, problem-solving skills, and the ability to collaborate with developers and other team members set exceptional testers apart. These skills ensure thorough identification and documentation of defects, leading to higher software quality and more efficient development cycles.

What are some common challenges manual QA testers face when testing new software releases?

Manual QA Testers often encounter tight deadlines, incomplete documentation, or rapidly changing requirements, which can make it challenging to thoroughly test new releases. Additionally, ensuring test coverage across multiple platforms and devices while identifying subtle bugs requires keen attention to detail and strong organizational skills. Effective communication with developers and product teams is crucial for clarifying requirements and reporting issues, making collaboration an essential part of the role.

What is the difference between Manual Qa Tester vs Automation Tester?

AspectManual Qa TesterAutomation Tester
Primary FocusExecuting test cases manually to identify bugsDeveloping and executing automated test scripts
Required SkillsAttention to detail, understanding of testing processesProgramming skills, scripting, familiarity with automation tools
Work EnvironmentTest labs, manual testing environmentsTest automation frameworks, scripting environments
CertificationsISTQB, CSTE often preferredISTQB, Certified Automation Tester certifications

Manual Qa Testers focus on manual testing processes, while Automation Testers develop scripts to automate tests. Both roles require understanding of testing principles and certifications like ISTQB, but differ mainly in technical skills and work methods.

How much does a manual qa tester make?

A manual QA tester's salary typically ranges from $40,000 to $80,000 annually, depending on experience, location, and industry. Entry-level testers usually earn less, while experienced professionals with certifications or specialized skills can earn higher salaries. Many testers also work in team environments using tools like Jira or TestRail and may require knowledge of testing methodologies and scripting basics.
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For Manual Qa Tester jobs in PR, the most frequently searched job titles are:

Manual Qa Tester jobs near you
Infographic showing various Manual Qa Tester job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Specialist QA

BioPharma Consulting JAD Group

Juncos, PR • On-site

Full-time

Re-posted 20 days ago

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.