CQV Validation Specialist — Pharma & MedTech

ECHO Consulting Group; Carolina (PR); On-site; USD 80,000 - 140,000; Full time

Job summary

ECHO Consulting Group is seeking Commissioning, Qualification, and Validation (CQV) professionals to support validation activities in regulated pharmaceutical, biotechnology, or medical device manufacturing environments. This role welcomes Engineers, Scientists, and Validation Specialists with experience validating equipment, utilities, laboratory systems, or facilities.

You will participate in protocol development, execution, and validation documentation, and ensure compliance with cGMP

Qualifications

• 5+ years of validation, commissioning, or regulated manufacturing experience.
• Knowledge of cGMP regulations and validation lifecycle.
• Experience supporting IQ/OQ/PQ execution or validation documentation.
• Strong technical writing and documentation skills.

Responsibilities

• Support CQV activities for validation projects.
• Develop, review, and execute IQ, OQ, and PQ protocols.
• Assist with equipment startup and commissioning activities.
• Author and review validation documentation, including protocols and reports.
• Ensure compliance with cGMP regulations and FDA guidelines.
• Participate in risk assessments and impact assessments related to validation.
• Support change control, deviations, and CAPA investigations.
• Collaborate with Engineering, Quality, Laboratory, Manufacturing, and Validation teams.
• Ensure GDP and data integrity principles.

Skills

CQV experience

Technical writing

Regulatory compliance

Education

Bachelor's degree in Engineering, Chemistry, Microbiology, Biology, or related science

Job description

ECHO Consulting Group is seeking Commissioning, Qualification, and Validation (CQV) professionals to support validation activities in regulated pharmaceutical, biotechnology, or medical device manufacturing environments. This role welcomes Engineers, Scientists, and Validation Specialists with experience validating equipment, utilities, laboratory systems, or facilities.

You will participate in protocol development, execution, and validation documentation, and ensure compliance with cGMP