CQV Engineer: Equipment Validation Specialist

Arcadis; Framingham (MA); On-site; USD 70,000 - 90,000; Full time

Job summary

A global EPCM firm is seeking a CQV Engineer to support projects in New Bedford, MA. The role involves developing and executing equipment validation protocols within a cGMP and FDA regulated environment. Candidates should have 3-5 years of Equipment Validation experience and a strong understanding of automated systems. The position also requires preparation of validation documentation and resolution of validation-related issues, ensuring compliance with industry standards.

Qualifications

• 3-5 years of Equipment Validation experience in a cGMP & FDA regulated environment.
• Experience with CQV activities for equipment.
• Strong understanding of equipment and automated systems.

Responsibilities

• Familiarize with user and functional requirements.
• Develop equipment validation protocols.
• Execute equipment validation protocols.
• Prepare validation documentation.
• Support resolution of validation-related issues.

Skills

Equipment Validation experience

cGMP & FDA knowledge

Protocol development

Documentation management

Job description

A global EPCM firm is seeking a CQV Engineer to support projects in New Bedford, MA. The role involves developing and executing equipment validation protocols within a cGMP and FDA regulated environment. Candidates should have 3-5 years of Equipment Validation experience and a strong understanding of automated systems. The position also requires preparation of validation documentation and resolution of validation-related issues, ensuring compliance with industry standards.