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Data Validation Jobs in Puerto Rico (NOW HIRING)

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Analyze validation data, investigate deviations, and recommend corrective actions when necessary. * Maintain compliance with cGMP, FDA, EMA, ICH, and company quality standards. * Support internal ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Analyze validation data, investigate deviations, and recommend corrective actions when necessary. * Maintain compliance with cGMP, FDA, EMA, ICH, and company quality standards. * Support internal ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Analyze validation data, investigate deviations, and recommend corrective actions when necessary. * Maintain compliance with cGMP, FDA, EMA, ICH, and company quality standards. * Support internal ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Analyze validation data, investigate deviations, and recommend corrective actions when necessary. * Maintain compliance with cGMP, FDA, EMA, ICH, and company quality standards. * Support internal ...

CIS International LLC

PR

Data collection and documentation * Equipment testing and verification * Utility and environmental ... Maintain validation documentation and ensure records are complete, accurate, and compliant with ...

CIS International LLC

PR · On-site

Directing protocol execution activities, including data collection, field sampling, data trending ... Monitoring, tracking, and communicating validation project status, risks, and deliverables to ...

Kelly Services

PR

$25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Collecting, analyzing, and documenting testing data and validation results. * Preparing and maintaining technical documentation, including protocols, reports, and test summaries. * Coordinating with ...

CIS International LLC

PR

Directing protocol execution activities, including data collection, field sampling, data trending ... Monitoring, tracking, and communicating validation project status, risks, and deliverables to ...

Veg Group

Data Scientist

Juncos, PR · On-site

$90 - $120/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Data Scientist Description: SUMMARY The Data Scientist will lead projects and collaborate with ...

New

QRC Group

Sr Data Scientist

Juncos, PR · On-site

$110 - $150/hr

Validation and/or GMP documentation experience. * Knowledge of GMP expectations, validation lifecycle activities, protocol/report development, documentation practices, data integrity, discrepancy ...

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Document test results and execution activities in accordance with applicable GMP and data integrity ...

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Showing results 21-40

All JobsData Validation JobsData Validation Jobs in Puerto Rico

Data Validation information

What is a data validation?

A Data Validation job involves reviewing, cleaning, and verifying data to ensure accuracy, consistency, and reliability. Professionals in this role check for errors, inconsistencies, and missing information using automated tools and manual techniques. They work with databases, spreadsheets, and software applications to maintain data integrity, often collaborating with analysts and engineers. Their work is critical for making informed business decisions and maintaining regulatory compliance.

What does a data validation do?

A Data Validation professional typically spends their day reviewing large datasets, identifying inconsistencies or errors, and ensuring that all data meets established quality standards. This may involve developing and running automated scripts, maintaining data validation rules, and collaborating with data engineers or analysts to resolve data-related issues. The role often requires documenting validation processes and findings to support transparency and future audits. You can expect to work both independently and as part of a larger data or QA team, making your contributions vital to maintaining reliable business information.

What are the key skills and qualifications needed to thrive in data validation, and why are they important?

To thrive in Data Validation, a strong attention to detail, analytical thinking, and experience with data management or quality assurance processes are essential, often supported by a degree in information technology, statistics, or a related field. Familiarity with database software (such as SQL), spreadsheet tools (like Excel), and data validation or ETL (Extract, Transform, Load) systems, along with relevant certifications, is highly beneficial. Strong problem-solving skills, effective communication, and the ability to work both independently and collaboratively help individuals excel in this role. These skills ensure the accuracy and integrity of organizational data, supporting informed decision-making and operational efficiency.

What is the work of data validation?

Data validation is a key responsibility in data validation roles, involving checking data for accuracy, completeness, and consistency to ensure it meets specified standards. It often requires knowledge of data management tools and techniques to identify errors and prevent incorrect data from entering systems, supporting data quality and integrity.

What are popular job titles related to Data Validation jobs in Puerto Rico?

For Data Validation jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Data Validation jobs in Puerto Rico look for?

The top searched job categories for Data Validation jobs in Puerto Rico are:

Data Validation jobs near you
Infographic showing various Data Validation job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Cleaning Validation Specialist

Moriah Engineering

Jayuya, PR

Contractor

Re-posted 3 days ago

Job description

Job Summary:


The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and internal quality standards. The role focuses on ensuring the effectiveness and consistency of cleaning processes, particularly for manufacturing equipment and related systems, including utilities and compressed air systems. The ideal candidate will bring expertise in cleaning validation, utilities qualification, and a strong understanding of GMP regulations.


Responsibilities:

Develop and implement cleaning validation protocols and reports, ensuring compliance with GMP, FDA, and other regulatory standards.
Plan and execute cleaning validation activities for manufacturing equipment and utilities, including compressed air systems.
Conduct risk assessments and identify critical control points for cleaning validation.
Perform sampling and testing of cleaned equipment and utilities to ensure compliance with predetermined acceptance criteria.
Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to define cleaning validation requirements and processes.
Develop and implement protocols for utilities qualification and monitoring, with a focus on compressed air systems.
Analyze data to identify trends and recommend process improvements to enhance cleaning and utilities validation performance.
Manage deviations and non-conformances related to cleaning validation activities, ensuring timely investigation and resolution.
Maintain detailed and accurate documentation of cleaning validation and utilities qualification activities.
Ensure the consistent implementation of cleaning validation processes across manufacturing operations.
Support audits and inspections by regulatory authorities, providing expertise in cleaning validation and utilities processes.
Stay current with industry trends and regulatory updates, ensuring continuous compliance and the adoption of best practices.

Qualifications:


Bachelor's Degree in Engineering, Chemistry, Microbiology, or a related field.
2+ years of experience in cleaning validation within a regulated manufacturing environment.
Experience in utilities qualification, particularly compressed air systems.
Strong knowledge of regulatory requirements, including GMP, FDA, and ICH guidelines.
Proficiency in developing and executing cleaning validation protocols and reports.
Demonstrated experience in risk assessment and data analysis for cleaning validation.
Excellent problem-solving and analytical skills.
Strong communication and interpersonal skills to collaborate with cross-functional teams and external auditors.
Proficiency in software tools such as MS Excel, Word, PowerPoint, and project management tools.
Physical/Mental Requirements:

Ability to work in a manufacturing environment, including cleanrooms and production areas.
Able to stand for extended periods and climb ladders/steps as needed.
Ability to lift and move items up to 25 lbs.


About the Company:
We consider all applicants for all positions regardless of race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or any other characteristic protected by law. We value diversity and promote an inclusive environment where all employees can thrive.

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