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Validation Associate Jobs in Puerto Rico (NOW HIRING)

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate Quality Analyst QUALIFICATIONS: * Bachelor's degree in Natural Sciences, preferably ...

New

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate EH&S Education: * Master degree or Bachelor degree & 2 years of directly related ...

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate Quality Analyst II Description: Responsible for implementing and maintaining the ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

PR · On-site

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

Associate or Bachelor's degree in Engineering, Construction Management, or related field (preferred). At Validation & Engineering Group, people always come first. We believe that when you're ...

PR

$20.25 - $28/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate's degree and 10 years of Engineering experience or * High school diploma / GED and 12 ...

PR

$102K - $140K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... engineers, associates and/or technicians on an ongoing basis as well as on a project basis. 4. ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate's or Bachelor's degree in Environmental Health & Safety, Industrial Hygiene, Engineering ...

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Validation Associate information

What is a validation associate?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

How does a validation associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.

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

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

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

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

What are popular job titles related to Validation Associate jobs in Puerto Rico?

For Validation Associate jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Validation Associate jobs in Puerto Rico look for?

The top searched job categories for Validation Associate jobs in Puerto Rico are:

Infographic showing various Validation Associate job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Full-time

Posted yesterday

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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:

  • Associate Quality Analyst

QUALIFICATIONS:

  • Bachelor’s degree in Natural Sciences, preferably Biology, Chemistry or related field.
  • Experience in a Quality or technical field in the Pharmaceutical or Biotechnological industry preferred.
  • Quality/compliance management skills as well as regulations and standards.
  • Position requires computer literacy to manage multiple computer programs and databases.
  • Knowledge of data processing system, analytical competence, good verbal and written communication skill in both languages, English and Spanish.
  • Prior experience in CAPA, Change Control, and/or Risk Management is preferred.

RESPONSIBILITIES:

  • Monitor performance through appropriate Key Performance Indicators (KPIs) for CAPA, Change Control, and Risk Management. Ensure a timely completion of actions identified in: Exception Reporting System, Change Management or Risk Management quality records and programs.
  • Provide leadership to ensure that actions are properly reviewed in order to ensure appropriate definition and timely completion of actions and review of significant trends/issues to prevent regulatory liabilities and financial losses.
  • Evaluate if actions were effective and verified after implementation. Confirm that actions do not adversely affect the finished product.
  • Maintain the required databases necessary for tracking and trending to ensure actions are implemented and documented.
  • Facilitate meetings to ensure timely identification and management of events, including but not limited to triage and CAPA review board.
  • Drive dialogue and discussion to ensure non-conformances are appropriately documented in a timely manner and that - when required - investigations are timely, rigorous and drive to root cause to facilitate the identification and implementation of effective corrections, corrective and preventive actions.
  • Provide in a timely manner information and analysis required for the Annual Quality Reviews, among other meetings.
  • Review and perform statistical analysis of all exception documents by reasons (re-inspections, NCR, Deviations and associated formal investigations). Correlate information and summarize it with the corresponding corrective actions. Identify if there are trends indicating the need for changes manufacturing or control procedures.

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.