Validation Engineer - Fairfield, NJ

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 ...

Weiss-Aug is seeking a passionate and skilled Validation Engineer to join our team and contribute to our mission of delivering high-quality, engineered solutions to our customers worldwide.We're currently looking for a candidate who will be responsible for Validation/PPAP Package ...

This role involves providing validation support for other systems and projects. It requires developing validation plans and protocols, tracking deviations, and coordinating testing efforts. ...

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 ...

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 ...

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. · ...

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. · ...

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 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. · ...

A Sr. CSV Engineer role at a Global Pharmaceutical Company with experience working with divestitures, mergers and acquisitions is required. · 7+ years' experience in Computer System Validation or Quality management or Business Analysis in GxP application area · Responsible to Aut ...

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 ...

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 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. · + · ...

This position involves writing and execution of validation protocols and reports. · ...

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 ...

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 ...

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 ...