MF01-020224 CQV PM

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 individuals committed to work under the highest ethics standards for the following positions:

• CQV Project Manager (1)
• CSV Specialist (3)
• Validation Specialist (5)

Qualifications:

• Bachelor's Degree in Science or Engineering.
• Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
• Experience with Computer System Validation (CSV), the Computer System Development Life Cycle (SDLC).
• Technical Writing skills.
• Available to work extended hours, possibility of weekends and holidays.