Principal Validation Engineer - Cranbury

The Senior Validation Engineer supports the successful operation of facility laboratory cGMP Manufacturing and business functions at WuXi Biologics sites throughout the United States through interaction with internal customers and external service providers. · ...

Joining us is a chance to do important work that creates change and shapes the future of healthcare. · ...

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 ...

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. · ...

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

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

Global Pharmaceutical Company · Sr. CSV Engineer Role - Hybrid (2-3 days onsite) · 7+ years' experience in Computer System Validation or Quality management or Business Analysis in GxP application area. · ...

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

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. · ...

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 ...

Maintaining qualified state of cleaning processes and procedures as well as design and implementation of new cleaning processes. · ...

A Validation Engineer is required to ensure compliance with client SDLC policies/procedures/templates and coach project teams on using the correct templates/SDLC processes. · ...

This role supports a New Product Introduction program focused on biologics manufacturing. · Lead all CIP and SIP validation activities for the NPI program · ...

We believe everyone has an opportunity to lead. We see the importance of your perspective and your ability to create value. · ...

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

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 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 ...

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 ...