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:

• Documentation Specialist

Qualifications:

• Bachelor's Degree in Administration or Science
• Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Must be proficient using MS Windows (Word, Excel, Power Point) and Outlook.
• Preferable experience with QualityDocs (QD)
• Preferable experience with SAP SuccessFactors
• Technical Writing skills
• Available to work extended hours, possibility of weekends and holidays.