Validation Specialist (Downstream Process Equipment) LL03-250822

Job Description

Job Description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas : Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position :

• CQV Specialist for Biotech Downstream Process Equipment

The CQV Specialist will support the commissioning and qualification of downstream process equipment for a GMP-compliant biotechnology manufacturing facility. The role involves hands-on execution of IQ / OQ / PQ protocols, system walkdowns, and validation documentation for equipment such as chromatography skids, TFF systems, ultrafiltration units, centrifuges, and bioburden reduction filtration systems. The ideal candidate will have prior experience with biotech processes, familiarity with regulatory standards (FDA / EU Annex 15), and the ability to work cross-functionally with engineering, QA, and operations teams.

Key Responsibilities :

Downstream Equipment in Scope :

Qualifications :

Preferred Skills :