CQV Validation Specialist — Pharma/Med Device

ECHO Consulting Group; United States; On-site; USD 95,000 - 125,000; Full time

Job summary

ECHO Consulting Group, Inc. seeks 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 supporting equipment, utilities, laboratory systems, or facilities qualification. The selected consultant will support protocol development, execution, and validation documentation, ensuring

Qualifications

• Bachelor’s degree in Engineering, Chemistry, Microbiology, Biology, or related scientific discipline.
• 5+ years of experience in validation, commissioning, qualification, or regulated manufacturing environments.
• 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.
• Develop, review, and execute IQ, OQ, and PQ protocols.
• Assist with equipment startup and commissioning activities.
• Author and review validation documentation, including protocols, reports, and discrepancy resolutions.
• Ensure compliance with cGMP regulations, FDA guidelines, and internal quality systems.
• Participate in risk assessments and impact assessments related to validation activities.
• Support change control, deviations, and CAPA investigations when required.
• Collaborate with Engineering, Quality, Laboratory, Manufacturing, and Validation teams.
• Ensure GDP and data integrity principles.

Skills

5+ years validation experience

Technical writing

Documentation skills

Education

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

Job description

ECHO Consulting Group, Inc. seeks 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 supporting equipment, utilities, laboratory systems, or facilities qualification. The selected consultant will support protocol development, execution, and validation documentation, ensuring