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Validation Jobs in Puerto Rico (NOW HIRING)

QRC Group

Validation Engineers

Caguas, PR · On-site

Caguas, Puerto Rico | Posted on 07/07/2026 We are seeking Validation Engineer professionals to support validation activities for sterile manufacturing, plant operations, facilities, equipment ...

Pinnaql

Validation Specialist

Aibonito, 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 Specialist

Aibonito, 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

Barceloneta, 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 Engineer

Barceloneta, PR • On-site

Validation & Engineering Group, Inc.
See more jobs at Validation & Engineering Group, Inc.external

Full-time

Re-posted 15 days ago

Key responsibilities

  • Develop, review, and execute validation protocols for aseptic filling lines, lyophilization, and support equipment.

  • Perform process validation activities related to sterile manufacturing, including media fills, and support commissioning and qualification activities for new equipment and facility upgrades.

  • Investigate deviations, CAPAs, and implement corrective actions related to validation activities.

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.

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