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:

• Validation Engineer & Quality Engineers:
  • Process validation experience- preferably with experience in the medical device industry.
  • Process development experience or good technical knowledge.
  • Medical Device documentation experience (FMEAs, change management, MES, etc.)
  • Know how to do basic troubleshooting of equipment. It is a differentiator to have knowledge of Software and/or PLC.

Qualifications:

• Bachelor's Degree in Science or Engineering.
• Minimum of 3 years of experience in the Regulated Industry.
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Must be proficient using MS Windows and Microsoft Office applications.
• Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
• Technical Writing skills and investigations processes.
• Available to work extended hours, possibility of weekends and holidays.