AVS is looking for a Validation resource for work in a biotech facility. This is a long term position. Responsibilities include but are not limited to the following: Performing installation qualification (IQ); operation qualification(OQ); performance qualification(PQ); Writing cGMP protocols and reports for qualification documents; Writing cGMP procedures for operation of equipment; Writing preventive maintenance plans for; Writing user requirement specifications; Initiating and leading change controls for implementation of new equipment. The individual must have 5 years of industry experience with 2 years of experience in CQV. The individual will also be responsible for authoring cGMP protocols, reports, equipment operation instructions, user requirements specifications, and preventive maintenance plans. The individual must have a Bachelors degree in engineering or science-related field.

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