Validation Engineer - Rahway

This role involves providing lab system administration and support via the ticketing system. The job requires collaboration with lab analysts and end users to confirm problems or requests. It also involves resolving issues or fulfilling requests onsite or remotely by following SO ...

The Associate Technical Operations within Global Clinical Supply GCS is responsible for managing aspects of equipment/project activities supporting infrastructure projects to establish upgrade modernize Clinical Supply Operations CSO facilities. · Flexible schedule. · ...

This role will track Clinical Supply Operations (CSO) equipment globally support qualification installation and release of new equipment and decommissioning of old equipment. · Track Clinical Supply Operations (CSO) equipment globally. · Support qualification installation and rel ...

The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multi-use sites through interaction with internal customers and external service providers. · ...

Maintains all qualified and validated equipment and systems in compliance with policies guidelines and procedures Develops protocols associated reports while adhering to a change management process Supports the execution of equipment qualifications and validation protocols Superv ...

The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multi-use sites through interaction with internal customers and external service providers. As a developing team player, the incumbent interacts with thei ...

The Equipment Validation Engineer supports the successful implementation of laboratory equipment at multi-use sites through interaction with internal customers and external service providers. · Maintains all qualified equipment systems in compliance with policies, guidelines and ...

The Equipment Engineer supports the successful operation of laboratory and clinical manufacturing operations at their home site. · PURPOSE AND SCOPE OF POSITION: The Equipment Engineer supports the successful operation of laboratory and clinical manufacturing operations at their ...

Drafting quality system documentation including SOPs and traceability matrix, · authorizing URS IQ OQ protocols compliance with GDP guidelines. · Coordinate validation activities vendors results draft reports. · Draft and implement Quality System documentation; · Author URS IQ OQ ...

The Equipment Validation Engineer supports the successful implementation of laboratory and manufacturing equipment and utilities at multi-use sites through interaction with internal customers and external service providers. · ,,,Maintains qualified equipment systems in compliance ...

We are seeking a Validation Engineer to support the successful implementation of various process/lab equipment at multi-use sites through interaction with internal customers and external service providers. · BS in Engineering or Science related discipline required. · Minimum of 5 ...

The Equipment Validation Engineer supports the successful implementation of various process/lab equipment at multi-use sites through interaction with internal customers and external service providers. · Maintains qualified equipment systems in compliance with policies, guidelines ...

The Equipment Validation Engineer supports the successful implementation of laboratory and manufacturing equipment and utilities at multi-use sites through interaction with internal customers and external service providers. · Knowledge of cGMP, GXP, GAMP, SDLC regulations, includ ...

Computerized Systems Validation (CSV) position involves ensuring that GxP-regulated computer systems and software comply with current Good Manufacturing Practices (cGMP) regulations, international guidelines and company standards by validating their functionality throughout their ...

You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. · ...

+The Validation Engineer is responsible for planning, executing, and documenting validation activities for medical device manufacturing processes, equipment, and systems to ensure compliance with FDA and ISO requirements. · + · ...

We are seeking a Validation Engineer with 4–7 years of relevant experience to support validation activities in a pharmaceutical/biotech environment. · We take a holistic view of sales and marketing, building digital brands that deliver real value to our client. · Maintain qualifi ...

A Validation Engineer position at Net2Source Inc. involves supporting computer system validation projects and equipment qualifications in a laboratory setting. · ...

Weiss-Aug is a leading provider of advanced manufacturing and engineering solutions with advanced facilities across the U.S. and Mexico for over 50 years.As a recognized leader in the industrial and commercial sectors, · specializing in high-volume metal stamping, · thermoplastic ...

Analyze validation test data to determine whether systems or processes meet validation criteria and identify root causes of problems for pharmaceutical facilities Prepare validation protocols for new processes Coordinate implementation of validation testing Create databases for t ...