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:

• CQV Scientist for Biotech Manufacturing Equipment

Qualifications:

• Bachelor's Degree in Science or Engineering.
• Minimum of 3 years of experience in direct pharmaceutical, medical device or preferably (biotechnology) industries.
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Experience in developing Systems Development Life Cycle (SDLC) documents such as VP, URS, DS, RA, IQ, OQ, PQ, TMX and so forth. Includes execution of protocols IOPQ, managing deviations, and reports generation.
• Preferably experience in the Biotech industry.
• Technical writing skills and investigations processes.
• Available to work extended hours, possibility of weekends and holidays.