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Validation Specialist at VEGA - ApplyBlast

Validation Specialist

VEGA

1 month ago

Aibonito, Puerto Rico, United States

Onsite

Full Time

Medior

0 applicants

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About this role

The Validation Specialist will develop, review, and execute Validation Master Plans and protocols such as IQ, OQ, and PQ for equipment, facilities, utilities, and cleanrooms. The role ensures validation documentation, risk assessments, and change controls are maintained in compliance with GMP and medical‑device regulatory requirements, while coordinating with cross‑functional teams to meet project milestones.

Responsibilities

Develop and execute Validation Master Plans and protocols
Validate equipment, facilities, utilities, and cleanrooms for compliance
Manage change controls, deviations, and CAPA investigations

Skills

Qualifications

Bachelor's degree in Engineering, Life Sciences, or related technical discipline

About VEGA

vega.com

Headquarters

Schiltach, Baden-Württemberg, Germany

Company Size

1001-5000 employees

Founded

1959

View Profile

VEGA Grieshaber KG designs and manufactures sensors and instrumentation for level, point level and pressure measurement. They provide both hardware and accompanying equipment and software for seamless integration into process control and automation systems. VEGA's solutions target industrial process applications worldwide, delivering reliable measurement for liquids, solids and bulk materials. The company emphasizes industrial-grade performance, integration capabilities and global service support.