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The CQV Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. Ideally experienced in 1 or more of the following: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC) upstream, downstream, purification, recovery, building automation or other pharmaceutical manufacturing processes.
$87,100 - $94,600 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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We are hiring an experienced and driven Facilities Engineer with 3-5 years of experience in Facilities Engineering within the pharmaceutical industry. Support and execute validation protocols for facilities, utilities, and equipment in compliance with GMP regulations.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. Must have experience in 1 or more of the following: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC) upstream, downstream, purification, recovery, building automation or other pharmaceutical manufacturing processes.
$87,100 - $94,600 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Will assist in integration events and validation of hardware and systems prior to aircraft integration, on-site as well as at Flight Operations facilities. We have an exciting opportunity for an entry level mechanical engineer within the GASI Mechanical Engineering Department.
$56,820 - $96,015 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Validation Process Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. We provide commissioning, qualification, validation, start-up, project management and other consulting services associated with operational readiness to FDA regulated and other mission-critical industries.
$87,100 - $94,600 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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From day one, you will work with various business units to design, develop, and usher production solutions for clients, both residential and commercial developments to mission-critical facilities.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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The Validation Engineer will be responsible for the execution of validation protocols for equipment, facilities, and processes, ensuring that all requirements are met. We are seeking a motivated Entry Level Validation Engineer to join our team for a 12-month contract in New Jersey.
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Leads cross-functional continuous improvement teams with Engineering, Validation, Quality Assurance, Quality Control, Facilities, Metrology, and Manufacturing Technical Services. Senior Manufacturing Compliance Engineer uses expert knowledge of compliance and GXP manufacturing processes to manage investigation and improvement initiatives within manufacturing operations.
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Lead site validation meetings, ensuring involvement, support and engagement from Engineering, Operations, site Water and C&S Teams, Technology Transfer/Quality Engineer, and Analytical and Microbiology Lab Supervisors and other customers as needed.
$80,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The engineer uses electrical and mechanical systems knowledge to inform the design of test stands, support facilities, avionics and control systems. General schematic capture and printed circuit board (PCB) design and/or verification and validation experience.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Validation Engineer is responsible for design, development and execution of C&Q (Commissioning & Qualification) activities for facilities, utilities, and equipment at the Elwood, Kansas monoclonal antibody (mAb) manufacturing site.
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Provide support for customer audits and external regulatory audits specific to validation activity at all Sharp facilities at the direction of the Validation Manager. Responsibilities include execution of all validation activities related to equipment, process and facilities qualifications at the direction of the Validation Manager.
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The Mission Defense Team (MDT) is seeking a highly motivated and qualified system engineer to serve as a Supplier Site Validation & Verification Engineer. Supplier Site Validation & Verification Engineer.
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Desc3 Building and Facilities Engineer. Obtain Architectural drawings and Certified Stamped drawings as required for any non Ford Land delivered, structural, fire protection and coordinate validation testing.
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Cellipont Bioservices is growing, and we are looking for an Senior Computer Systems Validation Engineer (CSV) who believes in the potential bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level.
$100,000 - $135,000 a yearExpandApply NowActive JobUpdated 2 days ago
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