Validation Engineer - Parsippany

· Full-time · Description · Join Weiss-Aug – A Leader in Precision Manufacturing and Innovation · Be part of a company that's shaping the future of manufacturing where your ideas, skills, and passion matter.  · Weiss-Aug, is a leading provider of advanced manufacturing and engin ...

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. · ...

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 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 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 ...

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 ...

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 ...

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 ...

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 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. · ...

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. · ...

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

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. · ...

· 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 ...

Our client, a Global Leader in the Medical Device Industry, has an immediate opening for a 2D Barcode Labeling Software Validation Engineer for a 12-month+ contract. Our client offers results-driven people a place where they can make a difference – every day You will also have th ...

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 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. · + · ...

Job Title: Validation Engineer · Location: Mahwah NJ · Duration: 12+ months of contract on W2 · Responsible for the design, modeling, development and testing of a machine, structure or system. Develops functional requirements. · Understands and applies standard engineering princi ...

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. · ...

· Benefits:401(k) · 401(k) matching · Bonus based on performance · Job Title: Validation Engineer (Contractor) · Location: Summit – West, New Jersey · Type: Contract · Job Description: · We are seeking a Validation Engineer with 4–7 years of relevant experience to support valida ...