The Equipment Validation Engineer (Process Equipment) is responsible for site-based engineering and validation support for CGMP cream & ointment process equipment and packaging lines and controls and ...

Senior Automation/Validation Engineer. Bachelor's degree in Electrical Engineering, Computer Science, or related field. We are a leading engineering and consulting firm partnering with prominent brand...

Three to six years of validation experience (or equivalent experience) in a cGMP environment with increasing levels of responsibility for a wide range of validation projects including validation of la...

Support cross functional teams in processing documents (assist in document editing, review, approvals).Document Control Management/Training processes.Revise SOPs related to Document Control/Training o...

Interface between Customer's engineering team and Internal engineering team concerning questions regarding engineering matters and vehicle configuration. The Integration engineer (Resident Engineer) i...

Prepare protocols and reports related to equipment/system/utility qualification (IQ/OQ/PQ), calibrations, engineering, process, packaging, and cleaning validations. Ability to read, write and interpre...

Provide mentorship to less experienced validation engineers in the team and handle projects assigned to validation contractors. Bachelor’s Degree in Engineering, Life Sciences, or related discipline, ...

BS in Engineering, Science, or equivalent technical degree.

Our client in Ramsey, NJ is hiring a Validation Engineer that will be responsible for preperation of validation protocols (IQ/OQ) and commissioning documents for their equipment and control systems. M...

Develops validation/qualification deliverables such as Validation Plans, Requirements. The Equipment Validation Engineer supports the successful implementation of various process/lab equipment at mult...

Analytical Validation Engineer. Analytical Validation Engineer. Compensation for the Analytical Validation Engineer.

The Junior Validation Engineer (Technical Services) is responsible for performing process validation, cleaning validation and equipment validation activities for solid dosage pharmaceuticals. Create a...

Support the development of the qualification and validation programs at Just including the transition from paper based to digital validation software to configure globally scalable end to end paperles...

User Acceptance testing, FAT, SAT, Validation Planning, IQ, OQ, PQ, Final Validation Summary Report. Support Client commissioning / validation for facility, utility, equipment, cleaning and process va...

Support validation activities for project activities including review of validation documentation (FAT, SAT, URS, SDS, IQ, OQ, PQ) and attendance at validation activities. Employee will be required to...

Experience with all pertinent industry best practices (, ISPE GAMP) including development and execution of all applicable system life cycle deliverables (, URS, SRS, FRS, DDS, RTM, Unit, Integration, ...

Key Words: Pharmaceutical Validation / New Jersey / Validation Engineer / Systems Validation / IQ / OQ / Validation Reporting / Pharmaceutical Engineer. As the Validation Engineer you will field execu...

Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls. Develops validation/qualification deliver...

Bachelors or masters degree in Pharmaceutical Sciences, Engineering, Microbiology or similar degree and a minimum of three (3) years of relevant experience performing validation activities within an a...

Modem system validation engineer. Partner with RF Engineering to help drive best-in-class RF network design to achieve the performance objectives.