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Data Validation Jobs in Puerto Rico (NOW HIRING)

Validation & Engineering Group, Inc

PR

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 ...

FITS LLC

Validation Specialist

Dorado, PR · On-site

Validation lifecycle and documentation * Regulated environments (FDA, ISO, GMP ... Data analysis tools * Document management systems The Personality Part: * Our Next Piece is someone ...

Biosimilar Sciences PR LLC

PR · On-site

Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico ... Operating as a cGMP incubator-style environment, OcyonBio enables robust CMC data generation to ...

FITS LLC

Validation Specialist

Dorado, PR · On-site

Validation lifecycle and documentation * Regulated environments (FDA, ISO, GMP ... Data analysis tools * Document management systems The Personality Part: * Our Next Piece is someone ...

PharmEng Technology Americas

PR · On-site

Analyze data, utilizing statistical methods, generated by validation studies performed by the Validation group to determine process capabilities. * Gather photocopies and compile relevant ...

Jedson Engineering Inc

PR · On-site

Include preparation of (IQ/OQ/PQ) protocols for packaging equipment, execution and documentation of validation studies, review of the raw data and development of the summary reports. Requires cross ...

Weil Group, Inc

Validation Specialist

Juncos, PR · On-site

Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Document execution activities in accordance with protocol instructions and data integrity ...

Weil Group, Inc

Validation Specialist

Juncos, PR

Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Document execution activities in accordance with protocol instructions and data integrity ...

Weil Group, Inc.

Validation Specialist

Juncos, PR · On-site

Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Document execution activities in accordance with protocol instructions and data integrity ...

PharmEng Technology Americas

PR · On-site

... analyze data and reach appropriate conclusions, and to perform and appropriately document ... Experience with validation and working knowledge of production is a plus. * Familiarity with FDA ...

Moriah Engineering

PR · On-site

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 ...

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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:
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 May 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 100% In-person job distribution.

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group, Inc

PR

Full-time

Posted 20 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 Specialist - CIP

Summary:
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems within a biotech manufacturing environment. This role ensures that cleaning and sterilization systems are installed, tested, and qualified in compliance with GMP, FDA, EMA, and ASTM E2500 standards, supporting readiness for process validation and commercial manufacturing.

Key Responsibilities:
Commissioning & Qualification Execution:

  • Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
  • Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam sterilization cycle qualification, and temperature mapping.
  • Oversee the qualification of utilities supporting CIP/SIP systems (Clean Steam, WFI, Process Air).
  • 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 in compliance with ASTM E2500 and GAMP 5.
  • Ensure traceability from design specifications through executed testing.
  • Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.
  • Prepare summary reports for Quality Assurance approval.


Cross-functional Collaboration:

  • Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.
  • Support operations during process validation batches and cleaning validation campaigns.
  • Provide training and technical guidance to CQV engineers and contractors executing test protocols.


Qualifications:

  • Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
  • Experience in generating and executing documentation for CQV activities.
  • Strong knowledge of cleaning validation, sterilization principles, and automation integration.
  • Familiarity with DeltaV, SCADA, or PLC systems for CIP/SIP recipe management.
  • Expertise in ASTM E2500, ISPE Baseline Guides, GAMP 5, and FDA/EMA guidelines.
  • Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
  • Experience executing or overseeing FAT/SAT, IOQ, PQ activities.
  • Knowledge of data integrity, 21 CFR Part 11, and electronic validation systems (e.g., Kneat, ValGenesis).
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • 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.