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:

• Document Controller
  • Coordinate and implement site projects associated with Engineering and SOP area.
  • Suppliers / contractors Qualifications Program
  • Effective procedure development
  • Development and/or review of Standard Operating Procedures (SOPs), Operational guidelines and related training materials ensuring compliance with the Corporate Standards and local procedures.
  • Handle document review request apply correct formatting
  • Consolidate comments from reviewers and approvers and monitor/support

Qualifications:

• Bachelor's Degree in Science.
• Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.
• Experience in direct process / manufacturing areas.
• 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.