Job Description :
Title: Equipment Validation Engineers

Work City/State: Andover, MA

Start Date: Dec 2017

Length of Contract: 2 years

Project Description: The contract is to cover all validation/commissioning/qualification resources for a new manu site project.

Consultant’s Day to day responsibilities: Supporting more Sr. Validation Engineers in writing/executing Equipment/Automation/Utilities validations.

Required Skills: At least 3 years experience with performing validations on Drug Manufacturing Equipment, Automation Systems (Delta V), and Utilities (HVAC, Water Sys, etc. A candidate with experience in only a couple of these areas would be fine.

· Have extensive field experience in operating and troubleshooting GMP utility systems, DeltaV automation systems and other GMP systems defined in the scope.

· A minimum of three full years in this type of work is required.

· Be knowledgeable in current GMPs and Data Integrity requirements.

· Have excellent verbal and writing communication skills. Highly organized and able to work with both management, operations staff, quality staff and other contractors.

· Be experienced in writing commissioning test plans, validation protocols, deviations, project change managements and validation summary reports.

Interview process: 1 Phone Screen
             

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