Engineering - Validation Engineer Validation Engineer - Rocky Mount

+ Validation Engineer needs BS degree in a technical discipline. + · Validation Engineer requires: strong project management, organizational, analytical, computer, writing and communication skills. · cGMP regulations and latest validation guidelines essential. ...

We are looking for a Validation Engineer II to join our team. The successful candidate will have experience in validating laboratory instruments and systems, including those with computerized systems attached. They will be responsible for ensuring that lab instruments adhere to n ...

We are seeking a Validation Engineer III to join our team at Net2Source Inc. · Serving as validation representative for laboratory instruments and partnering with the laboratories, Quality System Administrators, Business Technology, Instrumentation and Quality Engineering on impl ...

We are one of the fastest-growing companies in the U.S. and this may be your opportunity to join us as a Validation Engineer II. · Serves as validation representative for laboratory instruments · ...

We are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position Validation Engineer Specialist. · ...

This role is responsible for providing advanced technical and engineering support to operations for equipment/system initial validation and requalification. · The role involves participating in equipment improvement teams to enhance compliance and performance of plant systems, · ...

This role is responsible for providing advanced technical and engineering support to operations for equipment/system initial validation and requalification. · ...

This role is responsible for providing advanced technical and engineering support to operations for equipment/system initial validation and requalification. ...

We are looking for a Validation Engineer for our client in Wilson, NC. · Participate in the commissioning, qualification and start-up of various pharmaceutical cGMP process and packaging equipment, utilities & facilities. · Coordinate, develop and prepare installation, operation ...

This role is responsible for providing advanced technical and engineering support to operations for equipment/system initial validation and requalification. · Schedule and participate in equipment requalifications per Standard Operating Procedures (SOPs). · Execute validation stu ...

This job involves hands-on experience with CSV in GxP environments for at least five years. · ...

Sr. Validation Engineer leads and manages C&Q lifecycle activities including URS, DQ, IQ, OQ, and PQ for automation and process systems. · ...

Join our client, a pharmaceutical company, as a Validation Specialist - Engineering. · ...

Lead and manage C&Q lifecycle activities including URS, DQ, IQ, OQ, and PQ for automation and process systems. · ...

This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, FDA requirements and company policy. · ...

This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, · FDA requirements.Participate in the commissioning qualification start-up various pharmaceutical cGMP process packaging equipme ...

Join our client in the pharmaceutical industry as a Validation Specialist - Engineering. With 5+ years of experience in commissioning, qualification, and validation of systems within the pharmaceutical/biotech industry, you will be responsible for implementing and coordinating eq ...

This position is responsible for the successful implementation and coordination of equipment and facilities validation programs in compliance to cGMPs, FDA requirements and company policy. · Participate in the commissioning, qualification and start-up of various pharmaceutical cG ...

This Process Validation Engineer provides direct validation support to pharmaceutical development and manufacturing operations under minimum supervision. · Bachelor's degree in a Technical or Life Sciences discipline with a minimum of two (2) years of experience in the pharmaceut ...

We are seeking a skilled Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. · ...