Validation Engineer - East Brunswick, NJ

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 ...

This is a Validation Engineer role that involves authorizing reviewing and approving CSV lifecycle documents including validation plans user requirements specifications risk assessments protocols and reports. The candidate will also coordinate execute testing activities such as U ...

· Full-time · Description · Key Duties & Responsibilities · Draft and implement Quality System documentation including SOPs and Traceability Matrix designed to establish good validation practices within the organization. · Author URS, IQ, OQ and PQ protocols and execute them in ...

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. · ...

We are seeking a Validation Engineer II to join our team. You will work with a team of industry experts to help the world's leading companies solve their most difficult problems. Your responsibilities will include developing and executing validation and FDA compliance related doc ...

The Validation Engineer I provides support in performing equipment qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal's quality requirements. · Assist in the preparation/ execution of Installation Qualification(IQ)/Operational Qualificati ...

The Validation Engineer I provides support in performing equipment qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal's quality requirements. · ...

The Validation Engineer I provides support in performing equipment, facility and utility qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal's quality requirements. · Assist in the preparation/ execution of Installation Qualification(IQ)/O ...

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

The Validation Engineer supports the successful implementation of laboratory equipment · and systems at multi-use sites through interaction with internal customers · and external service providers.The incumbent in this role contributes to the completion of milestones associated ...

Writing and execution of validation protocols and reports (i.e. IQ, OQ, PQ, etc.) Developing manufacturing processes preparation of specifications process studies production readiness investigations root cause analysis problem solving report presentation preparation. · ...

Job Qualification: · • Experience in validating laboratory and labeling systems · • 5+ years' experience with System Development Lifecyle 10+ years' experience in Computer System Validation (Based on the role selected) · • Experience in FDA and/or Global regulated environment wit ...

We are seeking a Validation Engineer (CQV – LCMS) to support an industry-leading pharmaceutical organization. · ...

Job Qualification: · • Experience in validating laboratory and labeling systems · • 5+ years' experience with System Development Lifecyle 10+ years' experience in Computer System Validation (Based on the role selected) · • Experience in FDA and/or Global regulated environment wit ...

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 ...

Piper Companies seeks Validation Engineer (CQV – LCMS) in Titusville to support pharmaceutical organization. · ...

+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. · + · ...

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. · ...

We are seeking experienced Validation Engineers with strong hands-on expertise in GMP Drug Product facilities to support the qualification of a new commercial sterile fill-finish line. · Key Responsibilities: · Execute IQ/OQ/PQ/EMPQ for drug product processing equipment · Perform ...

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 ...