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Validation Associate Jobs in Puerto Rico (NOW HIRING)

PR

$57K - $58K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate CSV - Periodic Review Scientist Position Summary The Associate CSV Periodic Review ...

PR · On-site

$59K - $60K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate CSV - Periodic Review Scientist Position Summary The Associate CSV Periodic Review ...

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

$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 Project Management, Construction Management, Engineering ...

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...

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 ...

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 ...

PR

$36K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Technical diploma/associate degree in Electrical, Instrumentation, Mechatronics, or Controls (or ...

PR

$36K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Technical diploma/associate degree in Electrical, Instrumentation, Mechatronics, or Controls (or ...

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 ...

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 ...

PR · On-site

$36K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Technical diploma/associate degree in Electrical, Instrumentation, Mechatronics, or Controls (or ...

PR

$36K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Technical diploma/associate degree in Electrical, Instrumentation, Mechatronics, or Controls (or ...

PR · On-site

$36K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Technical diploma/associate degree in Electrical, Instrumentation, Mechatronics, or Controls (or ...

PR · On-site

$36K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Technical diploma/associate degree in Electrical, Instrumentation, Mechatronics, or Controls (or ...

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 ...

PR · On-site

$28K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Technical diploma/associate degree in Electrical, Instrumentation, Mechatronics, or Controls (or ...

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Validation Associate information

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.

How much does a validation specialist make in the US?

A validation specialist in the US typically earns between $60,000 and $85,000 annually, depending on experience, industry, and location. Entry-level roles may start around $50,000, while experienced professionals with certifications can earn over $100,000. Skills in quality assurance, regulatory compliance, and validation tools are often required for higher salaries.

What job makes $10,000 a month without a degree?

A Validation Associate typically does not earn $10,000 a month without a degree; such high earnings are uncommon for this role. Generally, jobs that can pay $10,000 monthly without a degree include specialized sales, real estate brokers, certain tech sales positions, or skilled trades with experience and commissions. These roles often require strong skills, certifications, or extensive experience rather than formal degrees.

Is QC a high paying job?

Quality Control (QC) roles, including validation associates, typically offer salaries that are average or slightly above average compared to other entry-level positions in manufacturing and healthcare industries. Compensation varies based on experience, location, and industry, with specialized skills and certifications potentially increasing earning potential.

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 Validation Associates?

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.

Is Associate the lowest position?

In the role of Validation Associate, this position is typically an entry-level or early-career role within the validation or quality assurance departments. It is often the starting point before advancing to higher roles such as Senior Validation Associate or Validation Specialist, depending on the company's structure and experience required. The lowest position in a validation or quality team may vary by organization but often begins with entry-level titles like Validation Associate or Technician.

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 most commonly searched types of Validation jobs in Puerto Rico? The most popular types of Validation jobs in Puerto Rico 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 June 2026, with employment types broken down into 67% Full Time, 32% Part Time, and 1% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution.

Associate CSV - Periodic Review Scientist

Validation & Engineering Group, Inc

PR

$57K - $58K/yr

Full-time

Posted 29 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:

  • Associate CSV – Periodic Review Scientist

Position Summary

The Associate CSV Periodic Review Scientist supports the execution of periodic reviews for GxP computer systems to ensure compliance with regulatory requirements and maintenance of the validated state. This entry-level role focuses on learning and applying validation principles, supporting risk-based assessments, and developing technical and compliance expertise in a GMP-regulated environment.

Key Responsibilities

  • Assist in the execution of Periodic Reviews (PR) for GxP computer systems under supervision.
  • Support the evaluation of:
    • Change controls, deviations, and CAPAs
    • System maintenance and calibration status
    • User access reviews and audit trails
    • Backup and restore processes
  • Help compile and organize documentation for PR reports.
  • Apply basic risk-based thinking to assess system status and identify potential issues.
  • Ensure documentation meets GDP (Good Documentation Practices) requirements.
  • Collaborate with cross-functional teams such as QA, IT, Engineering, and Operations.
  • Support audit and inspection readiness activities.
  • Follow procedures aligned with 21 CFR Part 11, EU Annex 11, and Data Integrity requirements.
  • Participate in training programs to build knowledge in CSV/CSA and GxP compliance.

Qualifications

  • Bachelor’s degree in:
    • Engineering (any discipline)
    • Computer Science / Information Systems
    • Life Sciences (Biology, Chemistry, Microbiology)
  • 0–2 years of experience in:
    • GMP environment, validation, IT, or quality (internships or co-ops acceptable)
  • Exposure to computer systems or regulated environments is a plus

Technical Skills

  • Basic understanding (or willingness to learn):
    • GxP regulations
    • Data Integrity (ALCOA+)
    • CSV/CSA concepts
  • Familiarity with:
    • Microsoft Office (Excel, Word, PowerPoint)
  • Exposure to GxP systems (SAP, LIMS, etc.) is a plus but not required

Preferred Qualifications

  • Internship experience in pharmaceutical, biotech, or regulated industries
  • Basic knowledge of validation lifecycle or system documentation
  • Exposure to audit or compliance activities

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.