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Senior Qa Analyst Jobs in Puerto Rico (NOW HIRING)

FITS LLC

Sr. Quality Engineer

Humacao, PR · On-site

$89K - $120K/yr

Conducts quality assurance tests. * Performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards. * Ensures that ...

Weil Group, Inc

Sr Quality Engineer

Humacao, PR

$89K - $121K/yr

Performs statistical analysis. Ensures that documentation is compliant with requirements. May ... Communicates with senior internal and external customers and vendors. Exchange information of facts ...

Weil Group, Inc.

Sr Quality Engineer

Humacao, PR · On-site +1

$89K - $121K/yr

Performs statistical analysis. Ensures that documentation is compliant with requirements. May ... Communicates with senior internal and external customers and vendors. Exchange information of facts ...

FITS LLC

Sr. Quality Engineer

Juncos, PR · On-site

$86K - $117K/yr

Conducts quality assurance tests. * Performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards. * Ensures that ...

Weil Group, Inc.

Sr Quality Engineer

Juncos, PR · On-site +1

$86K - $116K/yr

... product quality. Develops manufacturing processes that are applicable to statistical process ... Analysis provided is indepth in nature and often provides recommendations on process improvements.

AbbVie

PR · On-site

Ensures quality control and quality assurance compliance across the manufacturing site. Serves as ... analytical test methods, test method validation, SOPs, batch records, and site service requests

AbbVie

PR

Ensures quality control and quality assurance compliance across the manufacturing site. Serves as ... analytical test methods, test method validation, SOPs, batch records, and site service requests

Validation & Engineering Group, Inc

PR

Specialist QA (5:00 pm - 5:30 am) SUMMARY Perform one or more of the following duties and ... Alert senior management of quality, compliance, supply, and safety risks. * Provide support and ...

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Senior Qa Analyst information

What does a senior QA analyst do?

A Senior QA Analyst is responsible for designing, implementing, and overseeing testing processes to ensure the quality of software products. They develop and execute test plans and cases, identify defects, and work closely with development teams to resolve issues. Senior QA Analysts often mentor junior team members and contribute to the improvement of quality assurance standards and practices. Their role is critical in delivering reliable and high-performing software to end users.

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

To thrive as a Senior QA Analyst, you need advanced knowledge of software testing methodologies, quality assurance processes, and a relevant degree or equivalent experience. Familiarity with test automation tools (such as Selenium, JUnit, or QTP), bug tracking systems, and experience with CI/CD pipelines are typically required. Strong analytical thinking, attention to detail, effective communication, and leadership abilities help you excel in both independent and collaborative environments. These skills ensure software reliability, efficient defect resolution, and the delivery of high-quality products.

How does a senior QA analyst typically collaborate with development and product teams during a project lifecycle?

A Senior QA Analyst frequently works closely with development and product teams throughout the project lifecycle to ensure software quality meets business requirements. This involves participating in requirement reviews, providing input on testability, and clarifying acceptance criteria with product owners. During development, they coordinate with developers to understand technical implementations and with product managers to validate user expectations. Senior QA Analysts also often lead defect triage meetings and communicate test results and risks, fostering a collaborative environment for efficient issue resolution.

What is the difference between Senior Qa Analyst vs QA Tester?

AspectSenior QA AnalystQA Tester
CredentialsTypically requires a bachelor’s degree in Computer Science or related field, with experience in QA methodologiesOften requires a high school diploma or associate degree, with basic knowledge of testing tools
Work EnvironmentInvolves planning, analysis, and coordination with development teams in a collaborative settingPrimarily focused on executing test cases and reporting bugs, often in a more task-oriented environment
Industry UsageCommonly used in software development, IT, and technology companiesWidely used across software, gaming, and app development industries

The main difference between a Senior QA Analyst and a QA Tester lies in their responsibilities and experience level. Senior QA Analysts typically handle test planning, analysis, and coordination, requiring more experience and technical knowledge. QA Testers focus on executing tests and identifying bugs, often with less experience. Both roles are essential in the software quality assurance process, but the Senior QA Analyst plays a more strategic and leadership role.

How much does a senior QA analyst make in the US?

A senior QA analyst in the US typically earns between $70,000 and $110,000 annually, depending on experience, location, and industry. They often have skills in automation tools and testing frameworks, which can influence salary levels.

What are top 3 skills for a senior QA analyst?

A senior QA analyst should have strong analytical and problem-solving skills to identify issues effectively, proficiency in testing tools and automation frameworks such as Selenium or JUnit, and excellent communication abilities to collaborate with development teams and document findings clearly. Additionally, experience with test planning, understanding of software development lifecycle, and attention to detail are essential for success in this role.

What are popular job titles related to Senior Qa Analyst jobs in Puerto Rico?

For Senior Qa Analyst jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Senior Qa Analyst jobs in Puerto Rico look for?

The top searched job categories for Senior Qa Analyst jobs in Puerto Rico are:

What are popular job titles related to Senior Qa Analyst jobs in PR?

For Senior Qa Analyst jobs in PR, the most frequently searched job titles are:

Senior Qa Analyst jobs near you
Infographic showing various Senior Qa Analyst job openings in Puerto Rico as of June 2026, with employment types broken down into 1% As Needed, 87% Full Time, 8% Part Time, and 4% Contract. Highlights an 84% Physical, 6% Hybrid, and 10% Remote job distribution.

Manager, Quality Assurance Scientist

FITS LLC

Manati, PR • On-site

Contractor

Posted 14 days ago

Job description

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 & six (6) years of experience in the Pharmaceutical Manufacturing industry.
  • Bilingual (English & Spanish)
  • Shifts: Work irregular hours, rotating shifts, weekends, and holidays when needed.
  • Experience in:
    • Quality Assurance & cGMP Compliance
    • GMP Document Approval
    • Investigation & Root Cause Analysis
    • Cross-Functional Collaboration

The Personality Part:
  • Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, consistently delivering top-quality results. Are you ready to Be The Piece?

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
  • Interfaces directly with manufacturing and/or support areas operations to ensure that appropriate procedures are in place, through the execution of thorough reviews of procedures against practice.
  • Leads and participates in the critical review of all documents associated with the manufacturing and/or support areas operations, release, packaging, and relevant activities in the operations areas.
  • Ensures that deviations in documentation related to OOS or process parameters outside filing or validation are investigated and resolved by thoroughly reviewing timely corrective actions.
  • Provides key technical guidance and oversight to manufacturing and/or support area operations (Sterile, Non-Sterile, QC Laboratories, Warehouse, Engineering, Supply Chain, MS&T, IM, among others) to ensure appropriate cGMPs are in place through quarterly, monthly, weekly, or daily operations audits, as applicable.
  • Ensures compliance with all procedures (SOP's) to avoid potential regulatory and compliance issues, including GDP and electronic systems compliance.
  • Provides scientific input into investigation management to ensure root causes and CAPAs are aligned with the opportunities identified, enabling a systematic approach.
  • Supports actively the investigation processes in manufacturing areas (Sterile and Non Sterile) and support areas such as Warehouse, QC laboratories, IT, MS&T, facilities, and utilities, providing coaching from a quality perspective.
  • Provides guidance on gaps identified from the review and actively participates in determining potential remediation activities.
  • Supports risk analysis process when required per procedures.
  • Evaluates product impact and provides lot disposition recommendations when an investigation is completed as needed.
  • Manages audit observation, investigations, change control, and CAPAs records in the applicable QMS on timely manner.
  • Provides technical guidance and quality assurance support in the transfer of new products and processes to maintain quality standards.
  • Participates in Manufacturing Alignment Teams (MAT) and Project Alignment Teams (PAT), department staff, planning, and change control board meetings, as required.
  • Evaluates documentation compliance, including data GDP compliance and electronic system data compliance, and its overall management requirements for all manufacturing and support areas, including QC laboratories, such as CR's, SOP's, BR's, Forms, Logbooks, BOM's, WPP's, qualification and validation Protocols, according to government regulations and clients Policies.
  • Provides support to the area QA Leader during the budget preparation activities.
  • Evaluates department performance indicators and develops the appropriate corrective actions if needed
  • Assists management during internal and regulatory agencies inspections (FDA, DEA, MCA, etc).
  • Develops sampling plans based on acceptance quality level criteria when additional or special testing is required.
  • Performs trend analysis to provide recommendations in order to improve the process and /or the product quality.
  • Supports Media Fill activities to ensure that both typical and atypical interventions are performed as established.
  • Supports the Annual Product Review elements for Quality events of manufacturing and environmental monitoring.
  • Evaluates and approves the instrumentation and equipment calibration records and critical area engineering drawings.
  • Reviews and approves equipment, utilities, and facilities qualification, and system life-cycle documentation.
  • Reviews and approves all process, product, and computer systems validation protocols and reports, change control documentation, redressing/reprocessing / rework operations, investigation reports related to manufacturing process and microbiology laboratory, and Annual Product Quality Review (APQRs) elements.
  • Approves or rejects procedures impacting drug products, raw material, or packaging components.
  • Verifies compliance with clients' policies and Guidelines.
  • Participates as quality representative or liaison in site projects
  • Performs pre-operational review form approval in the manufacturing and packaging area.
  • Performs shop floor walk-through audits and challenges adherence to area procedures, providing coaching and Quality Support in alignment with the business unit to optimize compliance and effectiveness.
  • Verifies consistency with other site procedures and/or specifications.
  • Reviews and approves investigations related to process, products, utilities, microbiology laboratory, and calibrations.
  • Approves Corrective and Preventive actions (CAPAs).
  • Approves or rejects specifications impacting drug products, raw material, or packaging components.
  • Ensures effective systems for equipment maintenance and calibration, and approves calibration requests.
  • Ensures the designation and monitoring of storage conditions for quarantine materials and products.
  • Reviews and approves procedures for processes, products, utilities, and laboratories.
  • Maintains management informed (via frequent written reports) of any problem that might affect the quality and/or timely release of materials

WHO WE ARE:
We are a Service Provider company different from the rest. We pride ourselves on how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities, and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented, and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device, and Manufacturing industry clients with top-notch quality talent. We're FITS!
Are you the Next Piece?

Apply