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Validation Jobs in Puerto Rico (NOW HIRING)

FITS LLC

Validation Specialist

Dorado, PR · On-site

For Validation services WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's in Engineering with five (5) years of experience in Validation activities within the Medial Devices Industry.

QRC Group

Validation Engineer

Caguas, PR · On-site

Caguas, Puerto Rico | Posted on 07/30/2026 We are seeking a Validation Engineer to support equipment validation activities in a medical device manufacturing environment (21 CFR Part 820 / ISO 13485)

QRC Group, LLC

Validation Engineer

Caguas, PR · On-site

Caguas, Puerto Rico | Posted on 07/30/2026 We are seeking a Validation Engineer to support equipment validation activities in a medical device manufacturing environment (21 CFR Part 820 / ISO 13485)

HR Works

Validation Specialist

Jayuya, PR · On-site

Overview Directly responsible for the execution of all automation & validation assignments to fulfill our client's needs. Support the design, implementation, troubleshooting, and validation of ...

QRC Group

Validation Specialist

Cidra, PR · On-site

Cidra, Puerto Rico | Posted on 08/06/2026 Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation ...

FITS LLC

Validation Specialist

Dorado, PR · On-site

For Validation services WHAT MAKES YOU A FIT The Technical Part: * Bachelor's in Life Sciences with five (5) years of experience in Validation activities within the Medical Devices Industry.

QRC Group, LLC

Validation Engineers

Caguas, PR · On-site

Bulk IPA Storagesystems validation. * Plant operationsand quality project validation scope. * Facilities-relatedvalidations for designated engineers, including HVAC, utilities, cleanroom, andBMS. Key ...

QRC Group

Validation Specialist

Aibonito, PR · On-site

Aibonito, Puerto Rico | Posted on 08/04/2026 We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes. Requirements * 3 to 5 ...

Pinnaql

Validation Engineer - Upstream

Manati, 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 ...

HR Works

Validation / CSV Specialist

Las Piedras, PR · On-site

We are seeking a Validation / CSV Specialist to support validation activities within a regulated pharmaceutical manufacturing environment in Las Piedras, Puerto Rico . The ideal candidate will have ...

HR-Work

Validation / CSV Specialist

Las Piedras, PR · On-site

We are seeking a Validation / CSV Specialist to support validation activities within a regulated pharmaceutical manufacturing environment in Las Piedras, Puerto Rico . The ideal candidate will have ...

QRC Group

Validation Engineer/Molding

Aibonito, PR · On-site

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

Pinnaql

Validation Engineer - Upstream

Juana Diaz, 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 ...

Veg Group

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 ...

Veg Group

Jr. Validation Specialist

Carolina, 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 ...

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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.

Validation Specialist

Dorado, PR • On-site

FITS LLC
See more jobs at FITS LLCexternal

Contractor

Re-posted 17 days ago

Job description

For Validation services
WHAT MAKES YOU A FIT:
The Technical Part:
  • Bachelor's in Engineering with five (5) years of experience in Validation activities within the Medial Devices Industry.
  • Bilingual: English and Spanish
  • Soft Skills: Great attitude and strong desire to learn new skills.
  • Shift: Administrative, and according to business needs.
  • Experience in:
    • Validation (OQ/PQ/TMV/IPM)
    • Quality Engineering or Manufacturing Engineering
    • Validation lifecycle and documentation
    • Regulated environments (FDA, ISO, GMP)
    • Data analysis tools
    • Document management systems

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, 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)
  • Utilize automated tools to extract and filter validation documentation (e.g., Windchill → Excel trackers)
  • Review and validate extracted data to ensure accuracy, completeness, and site alignment
  • Execute detailed assessments across: OQ (Operational Qualification), PQ (Performance Qualification), TMV (Test Method Validation) and IPM (In-Process Monitoring).
  • Apply technical judgment to: Confirm applicability of validation documentation and identify discrepancies such as missing, conflicting, or outdated records.
  • Ensure alignment with: Current procedures, global validation standards and Remediation expectations and timelines.
  • Validate that extracted data accurately reflects site practices and documentation
  • Cross-check validation records against MVPs (Master Validation Plans), PRAs (Product Risk Assessments) and Supporting validation documentation.
  • Identify and quantify products requiring remediation across OQ, PQ, TMV, and IPM.
  • Highlight high-risk, complex, or ambiguous scenarios requiring deeper analysis.
  • Proactively identify: Data gaps, Inconsistencies and tool limitations.
  • Escalate risks, uncertainties, or blockers to the core team in a timely manner.
  • Provide clear documentation of findings and recommended actions.

WHO WE ARE:
We are a Service Provider company different 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 industry clients with top-notch quality talent. We're FITS!
Are you the next piece?

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