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Validation Jobs in Puerto Rico (NOW HIRING)

FITS LLC

Laboratory Validation Specialist

Anasco, PR · On-site

For Laboratory Validation Specialist services in the Quality Assurance/Validation area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's Degree inLife Sciences or related disciplineand at least ...

Techengpr

Cleaning Validation Specialist

Carolina, PR · On-site

We are seeking a Cleaning Validation Specialist to support critical manufacturing operations at the solid dosage manufacturing site. This role will play a key part in cleaning validation program ...

Pinnaql

Validation Engineer - Upstream

Juncos, PR · On-site

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 ...

Pinnaql

Validation Engineer - Upstream

Humacao, PR · On-site

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 ...

Pinnaql

Validation Engineer - Upstream

Humacao, PR · On-site

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 ...

QRC Group

Validation Engineer/Molding

Caguas, PR · On-site

Aibonito, Puerto Rico | Posted on 06/29/2026 We are seeking a Validation Specialist tosupport validation activities within the Injection Molding area. The selected candidatewill assist in the ...

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Validation information

What is a validation job?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What does a validation specialist do?

A validation specialist is responsible for ensuring that processes, equipment, and systems meet regulatory standards and quality requirements. They develop, execute, and document validation protocols, often working with industries like pharmaceuticals, biotech, or manufacturing, and may use tools such as validation software and perform risk assessments. Certification and attention to detail are important in this role.

What are the most commonly searched types of Validation jobs in Puerto Rico?

The most popular types of Validation jobs in Puerto Rico are:

Validation jobs near you
Infographic showing various Validation job openings in Puerto Rico as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, and 4% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Laboratory Validation Specialist

Anasco, PR • On-site

FITS LLC
See more jobs at FITS LLCexternal

Other

Posted 22 days ago

Job description

For Laboratory Validation Specialist services in the Quality Assurance/Validation area.

WHAT MAKES YOU A FIT:

The Technical Part:

  • Bachelor's Degree inLife Sciences or related disciplineand at least two (2) years of previous exposure to laboratory qualification, validation, and lifecycle management activities within the Pharmaceutical or Medical Devices industry.
  • Bilingual, Spanish and English (good communication)
  • Shift: Administrative & according to business needs
  • Experience in:
    • Computer System Validation (CSV), including ST and UAT execution.
    • Laboratory Equipment Qualification, Laboratory Instrumentation, and Equipment Lifecycle Management.
    • Data Integrity (ALCOA+), GMP, GDP, GxP, and 21 CFR Part 11 compliance requirements.
    • Change Control, Risk Assesments, and FMEA methodologies.
    • LIMS, Empower, and Validation Documentation development, review and execution.

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 your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge?

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)

  • Support qualification, validation, and lifecycle management activities for laboratory equipment and computerized systems.
  • Execute and review validation deliverables, including protocols, test scripts, reports, and traceability documentation.
  • Support Computer System Validation (CSV) activities in compliance with internal procedures and regulatory requirements.
  • Coordinate and execute System Testing (ST) and User Acceptance Testing (UAT) activities.
  • Support qualification activities for laboratory instruments and associated software applications.
  • Maintain validation documentation in an audit-ready state and ensure compliance with GMP, GDP, GxP, and 21 CFR Part 11 requirements.
  • Participate in risk assessments using FMEA and other risk-management tools.
  • Support change control activities and assess validation impact for system and equipment modifications.
  • Ensure compliance with Data Integrity (ALCOA+) principles throughout system and laboratory processes.
  • Collaborate with Quality, Laboratory Operations, IT, Validation, and Engineering teams to support project execution and ongoing compliance.
  • Assist with investigations, corrective actions, and continuous-improvement initiatives related to validated laboratory systems.
  • Support regulatory inspections and internal audits as required.

WHO WE ARE:

We are a Service Provider companydifferent from the rest. We pride ourselves in 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 industryclients with top-notch quality talent.We're FITS!

Are you the next piece?

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