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:

• SOP Writer

Qualifications:

• Bachelor's Degree in Science.
• Minimum of 2 years of experience in direct pharmaceutical, medical device, or biotechnology industries.
• Knowledge of QualityDocs (Veeva) System.
• Knowledge of SuccessFactor System.
• Proficient using MS Excel, Word and PowerPoint.
• Knowledge of Outlook and Teams.
• Ability to coordinate training sessions.
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Must be proficient using MS Windows and Microsoft Office applications.
• Knowledge in cGxP and regulatory guidance.
• Technical Writing skills and investigations processes.
• Available to work extended hours, possibility of weekends and holidays.