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Junior Validation Engineer Jobs in Puerto Rico (NOW HIRING)

JT630 - SR ENGINEER

Juncos, PR · On-site

$102K - $140K/yr

... Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams. * Interface with system owners and technical authorities. * Provide technical guidance and mentorship to junior engineers ...

Sr. Engineer- 35630

Juncos, PR · On-site

$150 - $200/hr

... Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams. * Interface with system owners and technical authorities. * Provide technical guidance and mentorship to junior engineers ...

Sr. Engineer- 35630

Juncos, PR · On-site

$125 - $150/hr

... Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams. * Interface with system owners and technical authorities. * Provide technical guidance and mentorship to junior engineers ...

PR · On-site

... junior engineers. * Coordination with other engineering disciplines and other cross-functional departments (automation engineering, facilities engineering, process engineering, validation, project ...

Equipment qualification & validation leadership (IQ/OQ/PQ) * Risk management tools (FMEA, Fault ... Mentoring or technical coaching of junior engineers * Strong technical writing (protocols, reports ...

Equipment qualification & validation leadership (IQ/OQ/PQ) * Risk management tools (FMEA, Fault ... Mentoring or technical coaching of junior engineers * Strong technical writing (protocols, reports ...

Equipment qualification & validation leadership (IQ/OQ/PQ) * Risk management tools (FMEA, Fault ... Mentoring or technical coaching of junior engineers * Strong technical writing (protocols, reports ...

Sr Cloud Security Architect

San Juan, PR · On-site

$150 - $200/hr

Develop and validate security policies, standards, and best practices, and author reusable ... Partner with solution architects and security engineering as an enabler, co-designing practical ...

Showing results 21-40

Junior Validation Engineer information

What does a junior validation engineer do?

A Junior Validation Engineer is responsible for assisting in the testing and verification of products, systems, or processes to ensure they meet specified requirements and standards. They typically work under the supervision of senior validation engineers and help develop validation protocols, execute tests, and document results. Their role is crucial in industries such as pharmaceuticals, manufacturing, and technology, where compliance and quality assurance are essential. Junior Validation Engineers also help identify issues and suggest improvements to enhance reliability and safety.

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

To thrive as a Junior Validation Engineer, you need a background in engineering or life sciences, strong analytical skills, and knowledge of regulatory standards like GMP. Familiarity with validation protocols, data analysis software, and documentation systems is typically required, and certifications such as Six Sigma or validation-specific training can be beneficial. Attention to detail, problem-solving, and effective communication are essential soft skills for collaborating with cross-functional teams and ensuring compliance. These skills and qualities are crucial for ensuring product quality, regulatory adherence, and the smooth execution of validation processes.

What are some typical challenges faced by a junior validation engineer during project execution?

As a Junior Validation Engineer, you may encounter challenges such as understanding complex validation protocols, managing tight project timelines, and adapting to strict regulatory requirements. You'll often need to collaborate closely with cross-functional teams, including quality assurance, manufacturing, and engineering, to ensure validation processes are thorough and compliant. Developing a keen attention to detail and strong communication skills will help you effectively address these challenges and contribute to successful project outcomes.

What is the difference between Junior Validation Engineer vs Validation Engineer?

AspectJunior Validation EngineerValidation Engineer
QualificationsTypically an entry-level degree (BSc or equivalent) in engineering, life sciences, or related fields; some certifications may be preferredHigher experience, often with professional certifications like CQE or CSQE
Work EnvironmentAssists in validation activities under supervision, often in regulated industries like pharmaceuticals or manufacturingLeads validation projects, responsible for planning and executing validation protocols independently
ResponsibilitiesPerforms routine validation tasks, documents results, supports senior staffDesigns validation strategies, reviews validation documentation, ensures compliance

The main difference between a Junior Validation Engineer and a Validation Engineer lies in experience and responsibility level. Junior Validation Engineers typically support validation activities under supervision, while Validation Engineers lead validation projects and make independent decisions. Both roles require knowledge of validation processes, but the Validation Engineer position demands more expertise and leadership in the field.

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

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

What cities in Puerto Rico are hiring for Junior Validation Engineer jobs?

Cities in Puerto Rico with the most Junior Validation Engineer job openings:

Infographic showing various Junior Validation Engineer job openings in Puerto Rico as of August 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 100% In-person job distribution.

JT630 - SR ENGINEER

Quality Consulting Group

Juncos, PR • On-site

$102K - $140K/yr

Contractor

Posted 12 days ago


Job description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
  • Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
  • Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.
  • C&Q Strategy & Planning
  • Develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements.
  • Define system boundaries and identify direct/indirect impact systems.
  • Lead risk assessments (e.g., ISPE Baseline, ASTM E2500) to determine qualification scope.
  • Develop C&Q plans, schedules, and resource forecasting.
  • Commissioning Activities
  • Oversee and/or execute commissioning activities including FAT, SAT, and field commissioning.
  • Ensure systems are installed and operate per design specifications.
  • Coordinate with vendors and contractors during startup activities.
  • Review and approve commissioning documentation and test results.
  • Qualification Execution (IQ/OQ/PQ)
  • Author, review, and approve qualification protocols (IQ, OQ, PQ).
  • Ensure traceability from User Requirements Specifications (URS) through testing.
  • Execute or oversee protocol execution and ensure proper documentation of results.
  • Documentation & Compliance
  • Ensure all C&Q documentation complies with GMP, FDA, EMA, and internal Amgen standards.
  • Maintain document lifecycle within electronic systems.
  • Support data integrity and ALCOA+ principles throughout qualification activities.
  • Prepare and support validation summary reports.
  • Risk Management & Change Control
  • Lead and document risk assessments related to system qualification.
  • Evaluate and manage change controls impacting validated systems.
  • Assess impact of deviations and implement corrective and preventive actions (CAPA).
  • Cross-functional Coordination
  • Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams.
  • Interface with system owners and technical authorities.
  • Provide technical guidance and mentorship to junior engineers and project team members.
  • Support project meetings, status reporting, and stakeholder communication.
  • Characterization Process
  • Develop the characterization protocols.
  • Execute the characterization activities.
  • Develop and review the characterization reports

Qualifications:
  • Bachelor's degree in Engineering
  • 4 + years of Engineering experience
  • Working knowledge of pharmaceutical/biotech processes
  • Familiarity with validation processes
  • Familiarity with documentation in a highly regulated environment
  • Ability to operate specialized laboratory equipment and computers as appropriate.
  • Ability to interpret and apply GLPs and GMPs.
  • Ability to apply engineering science to production.
  • Able to develop solutions to routine technical problems of limited scope
  • Negotiation, persuasion and facilitation
  • Collaboration
  • Project cost development
  • Conflict Resolution
  • Leadership and teambuilding
  • Management of contractors and vendors

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.