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Verification And Validation Engineer Jobs in Puerto Rico

Associate Engineer

San Juan, PR ยท On-site

$21/hr

... of verification/validation activities. Education and Experience: * Bachelor Science or Bachelor Engineering, Electrical, Software, or Mechanical Engineering. * Curriculum trains students in the ...

... of verification/validation activities. Responsibilities: * Design, communicate, and implement an operational plan for completing the project. * Monitor progress and performance against the project ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Previous Amgen CQV or verification experience. * Experience with OSIsoft PI / PI ProcessBook or PI ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Verification Lead. * Coordinate Technical Leads and CQV resources supporting cleaning and ...

Validation Specialist

Jayuya, PR ยท On-site

$60 - $80/hr

This role applies engineering principles and validation protocols to ensure compliance with cGMP ... Perform inspections and verifications of automated systems based on approved execution protocols ...

Showing results 21-40

Verification And Validation Engineer information

What is a verification and validation engineer?

Verification and Validation Engineers are professionals responsible for ensuring that products, systems, or software meet specified requirements and function as intended. They design and execute tests, review documentation, and analyze results to confirm that deliverables are both built correctly (verification) and serve their intended purpose (validation). Their work is crucial in highly regulated industries like aerospace, automotive, and healthcare, where safety and compliance are critical. These engineers collaborate with development teams to identify defects early and help ensure that projects meet quality standards before release.

What skills and qualifications are needed to thrive as a verification and validation engineer?

To thrive as a Verification and Validation Engineer, you need a solid background in engineering principles, software or hardware testing methodologies, and a relevant degree such as in electrical, computer, or systems engineering. Familiarity with test automation tools (e.g., Selenium, Jenkins), scripting languages, and standards like ISO or IEEE V&V processes is commonly required, along with certifications such as ISTQB. Attention to detail, analytical thinking, and strong communication skills set top performers apart by enabling thorough test coverage and clear reporting. These skills are essential to ensure products meet quality standards, regulatory requirements, and customer expectations before release.

How does a verification and validation engineer typically interact with development and QA teams during a project?

A Verification and Validation Engineer works closely with both development and QA teams to ensure that products meet specified requirements and function as intended. They often review design documents, develop test plans, and execute test cases in collaboration with developers, providing feedback on potential issues early in the process. Regular communication and coordination with QA are essential to ensure comprehensive test coverage and resolve defects efficiently. This collaborative approach helps maintain product quality and supports a smooth development lifecycle.

What is the difference between Verification And Validation Engineer vs Quality Assurance Engineer?

AspectVerification And Validation EngineerQuality Assurance Engineer
CredentialsTypically requires engineering degrees, certifications like ISTQB or ASQ CQEOften holds degrees in engineering, quality management, or related fields; certifications like Six Sigma or ISTQB
Work EnvironmentWorks in product development, testing labs, and manufacturing settingsWorks across development, production, and process improvement environments
Industry UsageCommon in electronics, aerospace, automotive, and medical device industriesWidely used in manufacturing, software, and service industries
FocusEnsures products meet specifications through testing and validationEnsures quality processes are followed to prevent defects

While both roles aim to ensure product quality, Verification And Validation Engineers focus on testing and confirming that products meet specifications, whereas Quality Assurance Engineers develop and maintain quality systems and processes to prevent defects. Both roles often collaborate but serve different stages of the product lifecycle.

Are verification and validation engineers in demand?

Verification and validation engineers are in high demand across industries such as aerospace, automotive, and software development, as companies prioritize quality assurance and regulatory compliance. These roles often require knowledge of testing methodologies, tools, and certifications, and employment opportunities are expected to grow with increased focus on product safety and reliability.

Do verification and validation engineers make good money?

Verification and validation engineers typically earn competitive salaries that vary by industry, experience, and location. They often require knowledge of testing tools, quality assurance processes, and sometimes certifications, which can influence earning potential. Overall, this role is considered well-compensated within engineering fields.

What are popular job titles related to Verification And Validation Engineer jobs in Puerto Rico?

For Verification And Validation Engineer jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Verification And Validation Engineer jobs in Puerto Rico look for?

The top searched job categories for Verification And Validation Engineer jobs in Puerto Rico are:

Infographic showing various Verification And Validation Engineer job openings in Puerto Rico as of August 2026, with employment types broken down into 59% Full Time, and 41% Contract. Highlights an 100% In-person job distribution.

Validation Specialist (Cleaning-In-Place)

Pinnaql

Juncos, PR โ€ข On-site

Full-time

Posted 21 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๏ฟฝ10 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.