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Verification And Validation Engineer Jobs in Puerto Rico

PR · On-site

Develop and execute validation/verification protocols for all commercial and R&D manufacturing ... Operations, Engineering, QA, laboratories (QC and R&D), and R&D to provide a high degree of ...

The Validation/Project Engineer is responsible for supporting New Product Introduction (NPI) and ... Kelly participates in E-Verify and will provide the federal government with your Form I-9 ...

The Validation/Project Engineer is responsible for supporting New Product Introduction (NPI) and ... Kelly participates in E-Verify and will provide the federal government with your Form I-9 ...

Inspect performance of machinery, equipment, and tools to verify their efficiency, and investigate ... Guide engineers regarding design concepts and specification requirements to best utilize equipment ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam ...

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Verification And Validation Engineer information

What are the key skills and qualifications needed to thrive as a Verification and Validation Engineer, and why are they important?

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.

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.

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 are Verification and Validation Engineers?

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 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:
What cities in Puerto Rico are hiring for Verification And Validation Engineer jobs? Cities in Puerto Rico with the most Verification And Validation Engineer job openings:
Infographic showing various Verification And Validation Engineer job openings in Puerto Rico as of June 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 75% In-person, and 25% Hybrid job distribution.

Validation Engineer

PharmEng Technology Americas

PR • On-site

Contractor

Posted 29 days ago


Job description

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning and Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products.

Job required Qualification:

  • Bachelor of Science degree, Engineering, or Equivalent training and experience.
  • More than 5 years of experience in a regulated environment.
  • 3 years of experience authorizing procedural and commercial marketing documents.
  • More than 3 years of experience with clean rooms, aseptic suites, single-use technology, bioreactors, and cell culture.
  • Experience in mechanic and Industrial engineering
  • Strong working knowledge of pharmaceutical industry regulations (GMP, GDP, ICH, etc.)
  • Strong understanding and working knowledge of project lifecycle, entrepreneurial mindset, and excellent written and verbal communication skills.
  • Strong relationship management, leadership, and organizational skills.
  • Strong working knowledge in Microsoft suites, and Smartsheet.

Job responsibilities and Duties:

  • Develop and execute equipment qualification protocols for all manufacturing, processing, and packaging equipment and facilities/utilities supporting these operations.
  • Develop and execute process validation protocols for all manufacturing and packaging processes of commercial products (and R&D products as applicable).
  • Develop and execute validation/verification protocols for all commercial and R&D manufacturing, processing, and packaging equipment.
  • Analyze data, utilizing statistical methods, generated by validation studies performed by the Validation group to determine process capabilities.
  • Gather photocopies and compile relevant documentation such as executed batch records, certificates of analysis, equipment logs, equipment qualifications, raw material certificates of analysis.
  • Investigate and resolve deviations/exceptions from the predefined acceptance criteria.
  • Draw conclusions from data, observations, deviation/exception, and investigation as to whether the process is considered valid.
  • Write summary reports (closeout report when applicable) for validation/qualification protocols following criteria as outlined within the validation/qualification procedures and policies.
  • Maintain protocols and system documentation in an orderly library so that information can be provided to regulatory bodies in a timely manner.
  • Ensure protocols, verifications, validation plans, and summary reports generated during validation/ qualification activities are stored according to the procedure.
  • Maintain current knowledge in the areas of compliance and validation and other regulatory issues that may impact the Company. Work proactively to maintain the highest level of compliance in all areas. Gather current knowledge from QA/QC, regulatory, periodicals, and/or appropriate training programs.
  • Interact and coordinate compliance efforts with other departments including, but not limited to, Operations, Engineering, QA, laboratories (QC and R&D), and R&D to provide a high degree of assurance that all qualification/validation activities, where appropriate, are completed.
  • Adhere to all cGMPs, compliance/regulatory mandates and quality requirements.
  • Perform other related duties as assigned to meet departmental and Company objectives.