Senior Validation Engineer - Piscataway

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 ...

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. · ...

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

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. · ...

The Validation Engineer III performs validation and engineering activities; conducts development studies; and monitors, analyzes and assists in improving pharmaceutical systems and processes. · ...

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 ...

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

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 minimum of 8 years' work experience in GXP / Analytical lab environment. · Bullet points for responsibilities and requirements are omitted to provide a concise summary. ...

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 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 ...

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

Piper Companies is seeking a Validation Engineer (CQV – LCMS) in Titusville, NJ to support an industry-leading 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 ISO requirements. · ...

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. · + · ...

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. · ...

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 ...