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Cqv Engineer Jobs in Puerto Rico (NOW HIRING)

Veg Group

CQV Project Manager

Juncos, PR · On-site

$125 - $150/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... CQV Project Manager Job Summary: We are seeking an experienced CQV Project Manager to lead the ...

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Pinnaql

CQV Project Manager

Juncos, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... CQV Project Manager Job Summary: We are seeking an experienced CQV Project Manager to lead the ...

MMR Consulting

PR

Its services include Engineering, Project Management, and Validation. MMRConsulting ... CQV Manager/PMwill require to lead commissioning, qualification, and validation activities for ...

MMR Consulting

PR · On-site

MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and ... This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and ...

Pinnaql

CQV Sample Management / LIMS Coordinator

Juncos, PR · On-site

$17.75 - $24/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... CQV Sample Management / LIMS Coordinator Job Summary: We are seeking an experienced CQV Sample ...

MMR Consulting

PR · On-site

MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and ... This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and ...

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Cqv Engineer information

What is a CQV engineer?

A CQV (Commissioning, Qualification, and Validation) Engineer is responsible for ensuring that equipment, systems, and processes within regulated industries, such as pharmaceuticals or biotechnology, meet regulatory and operational requirements. They develop and execute test protocols, troubleshoot issues, and document compliance with industry standards (e.g., FDA, GMP). Their role ensures that manufacturing facilities produce safe and effective products. CQV Engineers often collaborate with cross-functional teams, including quality, engineering, and operations.

What are the key skills and qualifications needed to thrive as a CQV engineer?

To thrive as a CQV (Commissioning, Qualification, and Validation) Engineer, you need a solid background in engineering principles, GMP regulations, and life sciences or pharmaceutical processes, often supported by a relevant degree. Familiarity with quality management systems, risk assessment tools, and software for documentation and validation such as TrackWise or Veeva is commonly required, and certifications like Six Sigma or CQV-specific credentials are valuable. Strong analytical thinking, attention to detail, effective communication, and collaboration skills set top performers apart. These competencies are essential to ensure compliance, project success, and seamless interaction with cross-functional teams in highly regulated environments.

What are some common challenges faced by CQV engineers in the pharmaceutical industry?

CQV Engineers in the pharmaceutical industry often encounter challenges such as managing strict timelines while ensuring full compliance with regulatory standards and adapting to evolving project requirements. They must coordinate with multiple departments including QA, production, and engineering to align project goals and documentation. Additionally, troubleshooting unexpected technical issues and staying updated with the latest industry guidelines can be demanding. However, overcoming these challenges is rewarding, as it directly contributes to the safe and effective delivery of life-saving products.

How much do CQV engineers make in the US?

CQV (Commissioning, Qualification, and Validation) engineers in the US typically earn between $80,000 and $130,000 annually, depending on experience, location, and industry. Senior or specialized engineers with certifications and extensive expertise can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory standards and validation tools.

What are popular job titles related to Cqv Engineer jobs in Puerto Rico?

For Cqv Engineer jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Cqv Engineer jobs in Puerto Rico look for?

The top searched job categories for Cqv Engineer jobs in Puerto Rico are:

Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in Puerto Rico as of August 2026, with employment types broken down into 72% Full Time, and 28% Contract. Highlights an 100% In-person job distribution.

STERILIZATION VALIDATION / CQV ENGINEER

Weil Group, Inc

Juncos, PR • On-site

$100 - $125/hr

Other

Posted 5 days ago

Job description

Position Summary

The Sterilization Validation/CQV Engineer will support development and execution of sterilization qualification activities involving autoclaves, SIP systems, thermometric studies, Biological Indicators, and associated sterilization cycles.

Key Responsibilities
  • Develop and execute Sterilization PQ protocols.
  • Prepare the corresponding Sterilization PQ final reports.
  • Review existing and new autoclave cycles and load configurations.
  • Support the qualification of new or modified sterilization cycles.
  • Coordinate thermometric studies, including thermocouple and Biological Indicator placement and retrieval.
  • Review temperature profiles, exposure times, lethality calculations, and other applicable cycle parameters.
  • Evaluate sterilization cycle results against approved protocol acceptance criteria.
  • Support sterilization conditional release activities as required.
  • Review SIP cycles, when applicable.
  • Generate and review PI Historian trends.
  • Identify and communicate any nonconforming or unexpected sterilization results.
  • Support investigations and technical assessments related to execution issues or discrepancies.
  • Coordinate execution activities with Manufacturing, Engineering, QC/Microbiology, and Quality.
  • Provide execution support during off-shifts, weekends, and extended-hour activities based on project needs.
  • Review sterilization calculations, data, and execution results as required.
Minimum Recommended Qualifications
  • Bachelor's degree in Engineering, Microbiology, Biotechnology, Life Sciences, or a related field.
  • At least 5 years of experience in validation within the pharmaceutical or biotechnology industry.
  • At least 3 years of experience supporting sterilization validation activities.
  • Hands‑on experience with autoclave qualification.
  • Experience with thermometric studies and the use of Biological Indicators.
  • Knowledge of SIP systems and sterilization cycle parameters.

Weil Group is proud to be an Equal Employment Opportunity Employer.

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