CQV Consultants – Engineering & Validation Professionals

QRC Group; Manatí (PR); On-site; USD 75,000 - 120,000; Full time

Job summary

QRC Group is seeking multiple CQV professionals to support ongoing projects in pharmaceutical, biotechnology, medical device, and other GMP-regulated environments. Positions cover commissioning, qualification, validation, and related documentation, with on-site work in Manatí, Puerto Rico.

You will join a multidisciplinary team and collaborate across Engineering, Operations, Quality, Validation, Automation, IT, Utilities, Maintenance, and Laboratory teams to ensure GMP compliance and timely

Qualifications

• Experience in pharmaceutical, biotechnology, medical device, or GMP-regulated industries.
• Knowledge of GMP, GDP, and applicable regulatory requirements.
• Experience supporting commissioning, qualification, validation activities.
• Strong writing, documentation, and organizational skills.
• Effective communication and cross-functional collaboration.
• Ability to work independently within a multidisciplinary project team.
• On-site work in Manatí, Puerto Rico.

Responsibilities

• Support planning, development, execution, review, and completion of CQV activities.
• Prepare, review, execute, or oversee qualification and validation protocols, assessments, traceability documentation, and final reports.
• Coordinate project activities and document review cycles with Engineering, Operations, Quality, Validation, Automation, IT, Utilities, Maintenance, and Laboratory teams, as applicable.
• Ensure that project deliverables comply with approved procedures, good documentation practices, GMP requirements, and applicable regulatory standards.
• Track assigned activities, deliverables, approvals, and project documentation through completion.
• Identify, document, escalate, and support the resolution of risks, deviations, change controls, and technical issues.

Skills

GMP knowledge

GDP knowledge

Regulatory compliance

Technical writing

Communication skills

Independent work

Education

Bachelor’s degree in Engineering, Science, or related technical discipline

Job description

CQV Consultants – Engineering & Validation Professionals

Manati, Puerto Rico | Posted on 10/16/2026

QRC Group is seeking multiple Commissioning, Qualification & Validation (CQV) professionals to support several ongoing projects. These opportunities support facility, laboratory, utility, automation, and computerized system improvement initiatives, requiring professionals with diverse CQV backgrounds and levels of experience.We are building a multidisciplinary team and are looking for qualified candidates across several technical areas.

Common Primary Responsibilities

• Support the planning, development, execution, review, and completion of commissioning, qualification, and validation activities.
  
• Prepare, review, execute, or oversee qualification and validation protocols, assessments, traceability documentation, and final reports.
  
• Coordinate project activities and document review cycles with Engineering, Operations, Quality, Validation, Automation, IT, Utilities, Maintenance, and Laboratory teams, as applicable.
  
• Ensure that project deliverables comply with approved procedures, good documentation practices, GMP requirements, and applicable regulatory standards.
  
• Track assigned activities, deliverables, approvals, and project documentation through completion.
  
• Identify, document, escalate, and support the resolution of risks, deviations, change controls, and technical issues.
  

Requirements

• Experience working in pharmaceutical, biotechnology, medical device, or another GMP-regulated industry.
  
• Knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and applicable regulatory requirements.
  
• Experience supporting commissioning, qualification, validation, or validation documentation activities.
  
• Strong technical writing, documentation, and organizational skills.
  
• Effective communication and cross-functional collaboration skills.
  
• Ability to work independently and as part of a multidisciplinary project team.
  
• Ability to manage assigned deliverables and maintain accurate, compliant, and timely documentation.
  
• Bachelor’s degree in Engineering, Science, Computer Science, or a related technical discipline, depending on the position.
  
• Ability to work on-site in Manatí, Puerto Rico, as required by the project.