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Data Validation Jobs in Puerto Rico (NOW HIRING)

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Ensure data integrity and adherence to 21 CFR Part 11 requirements (if applicable to systems)

PR · On-site

This role will ensure data accuracy, completeness, and alignment with current validation and remediation requirements. Utilize automated tools to extract and filter validation documentation, review ...

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

PR · On-site

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity. Documentation & Compliance: * Generate and review URS, FAT/SAT, IOQ, and PQ documentation ...

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Showing results 1-20

Data Validation information

What are the key skills and qualifications needed to thrive in the Data Validation position, 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 a Data Validation job?

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 are the typical daily responsibilities of someone working in Data Validation?

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 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:
Infographic showing various Data Validation job openings in Puerto Rico as of May 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 100% In-person job distribution.

Full-time

Posted 13 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Engineer

Description:

We are seeking a Validation Engineer with hands-on experience in biotech/pharmaceutical manufacturing, specifically supporting aseptic filling operations (vials). This role will be responsible for executing and supporting validation activities for equipment, processes, and computerized systems in compliance with regulatory requirements and industry standards.

Responsibilities:

  • Develop, review, and execute validation protocols including IQ, OQ, PQ for:
    • Aseptic filling lines (vial filling, stoppering, capping)
    • Lyophilization (if applicable)
    • Support equipment (autoclaves, washers, depyrogenation tunnels)
  • Perform process validation activities related to sterile manufacturing, including media fills (APS).
  • Ensure compliance with cGMP, FDA, EMA, and ICH guidelines.
  • Support commissioning and qualification (C&Q) activities for new equipment and facility upgrades.
  • Generate and review:
    • Validation master plans (VMPs)
    • SOPs, protocols, and final reports
  • Collaborate with cross-functional teams (Manufacturing, QA, Engineering, MSAT).
  • Investigate deviations, CAPAs, and implement corrective actions related to validation activities.
  • Support risk assessments (FMEA, impact assessments) for validation scope.
  • Ensure data integrity and adherence to 21 CFR Part 11 requirements (if applicable to systems).

Qualifications:

  • Bachelor’s degree in Engineering, Chemistry, Biology, or related field.
  • 3–7+ years of validation experience in biotech or pharmaceutical industry.
  • Strong experience with:
    • Aseptic processing
    • Vial filling operations
    • Sterile manufacturing environments
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.