Validation Engineer
Xyntek Incorporated, a CXV Global Company
Job Title
Validation Engineer
Job Description
Catalyx Services, LLC seeks a Validation Engineer reporting to office in Montgomeryville, PA to prepare various control systems validation documents, including user requirement specifications, functional requirements specifications, and detailed design specifications. Prepare and execute validation protocols and installation qualification protocols. Configure, program, test, and troubleshoot PLC. Configure, validate, design, and test DCS. Work on a variety of programmable logic controller systems and a variety of Distributed Controls Systems (DCS). Configure, validate, and test the Human Machine Interface (HMI) systems with the control systems. Design, program, test, validate, and maintain process controls and automation systems, including selecting the control system. Provide technical specifications for the control system, such as hardware and software specifications. Select the networking interface required to connect the control system to the process to be controlled, handling multiple projects concurrently. Requirements Qualified candidates must have a bachelor's degree in Electrical Engineering, Electronic Engineering, or a foreign equivalent and at least three (3) years of experience as an Automation Engineer or a substantially similar position performing all the duties as listed above. Relocation to client sites at various unanticipated client locations throughout the US is possible. Not a position that requires travel for work. Relocation costs not paid.
$96k - $144k
...position. The Company will accept applications on an ongoing basis until the position is filled.What will you do?As an EMS Validation Engineering Lead, you will play a lead role in ensuring Schneider Electric’s (SE’s) Environmental Monitoring System (EMS) deployment meets...SuggestedOngoing contractFull timeTemporary workWork at officeRemote workFlexible hours$120k - $180k
...Job Description Job Description Job Title: System Integration & Test Engineer (Optical Transport Networks) Job Description This role focuses on system integration and validation testing for next-generation optical transport platforms. You will help build a North...SuggestedPermanent employmentRemote work- ...Kashiv BioSciences, LLC in Piscataway, NJ is seeking a Validation Engineer III to develop, test, and implement validation solutions in a regulated environment. You will draft protocols, coordinate with vendors, and support technology transfer while maintaining compliance...Suggested
- ..., partners, and shared purpose fuel our work to advance patient care and access to important medicines. Position Summary The Validation Engineer III is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway, NJ. This employee will be...SuggestedFull timeContract workLocal areaFlexible hours
$72.8k - $80.1k
...workDirect small teams in document development and/or executionQualifications and Experience- Bachelor's degree in a science or engineering field (or equivalent experience)- 2–4 years' experience in commissioning and qualification in a regulated industry- Familiarity with...SuggestedWorldwide- ...Validation Specialist (Life Sciences)Develop and maintain SOPs, user manuals, validation protocols, and regulatory submission documents.Translate complex scientific and technical concepts into clear, concise documentation.Collaborate with SMEs to gather and verify technical...
$115k - $140k
...Test And Validation Engineer As a Test and Validation Engineer for TE Connectivity you will focus on test system design and verification-validation testing of high-speed products in cable assemblies targeting high speed communications and connectivity within datacenters...Work experience placementLocal area- ...Job Description Job Description Role Purpose: Validation Engineer: Support site commissioning and qualification, which includes but is not limited to the following: equipment, utilities, cleaning, process, assay qualifications. Ensuring the timely development, execution...Local area
- ...Responsibilities:Write and execute commissioning, qualification, & validation protocols for facilities, utilities, and process equipment.... ...:Degree in Chemical, Mechanical, or Biochemical Engineering.Minimum of 3 years of experience writing and executing CQV in...Work at office
- ...This role will be responsible for equipment/facility/computer validation projects in a hands‑on role including writing validation... ...facility, utilities, or computerized systems). Bachelor’s degree in engineering, life sciences, computer science, or a related technical...For contractorsLocal area
- GSK in King of Prussia, PA, seeks a hands-on Validation Lead to manage equipment, utility, and computer system validation projects. You will write protocols, execute tests, analyze data, and deliver final reports, representing validation on project teams. Ideal candidates...
$140k - $155k
...Job Title: Principal System Verification Engineer – Optical Networking Job Description This role focuses on system-level verification... ..., detailed test case development, automation, and customer validation activities across DWDM, ROADM, and OTN-based solutions. The...Permanent employment$89.27k - $130.93k
...material difference-makers to join our growing team. Interested? Learn more at .Overview:We are seeking a hands-on Manufacturing Engineer, who will be a technical expert directly responsible for the development, construction, and refinement of product prototypes and initial...Immediate start- ...Validation Specialist II The Validation Specialist II coordinates and implements various activities for compliant and effective support... ..., and Product/Process Development, Manufacturing and Quality Engineering groups. Assist Validation Manager provide oversight of the...
- ...departments.• 24/5+ support of manufacturing lines.• Other duties as assigned.Education and Experience• Bachelor of Science (or higher) in Engineering. Preferred degrees in Mechanical or Chemical Engineering.• 2+ years of experience in process engineering role preferred.• Hands-...Work at officeLocal areaWorldwideShift work
- ...01446 Job Description: We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities in... ...regulatory inspections and internal/external audits. Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, and Regulatory...
- ...high-tech environment, where your contributions make a real impact, we’d love to hear from you! Job Purpose The Manufacturing Engineer I is responsible for development, implementation, and maintenance of manufacturing processes for lithium batteries of different...Permanent employmentTemporary workLocal areaFlexible hours
- ...update key documentation, and lead projects aimed at improving efficiency and compliance. Qualifications include a B.S. or B.A. in Engineering or Sciences, strong technical writing skills, and experience in a manufacturing environment. This position may require...
- Merck & Co. in West Point, PA, seeks an Associate Specialist, Engineering, to support production of live virus vaccines and lead investigations of manufacturing deviations within the Live Virus Vaccine Manufacturing End-to-End. The role focuses on deviation management,...Shift work
- Merck is seeking a Senior Specialist, Engineering at the West Point site to lead investigations stemming from manufacturing deviations in live virus vaccine operations. The role focuses on root-cause analysis, corrective actions, and robust documentation, with cross-functional...
- Merck’s Manufacturing Leadership Development Program (MLDP) is a flagship global manufacturing graduate program. Over three years, you will rotate across core manufacturing functions, gain real-world experience, and be mentored by senior leaders to build both technical ...
- Merck is seeking an Associate Specialist, Engineering to support live virus vaccine production at the West Point site. The role leads investigations, identifies root causes, and develops corrective actions within the Deviation Management team in Technical Operations. Strong...
- Merck is seeking an Engineering Specialist to support live virus vaccine production at the West Point site, focusing on deviation investigations... ..., work with cross-functional teams, and prepare technical documentation and validation activities as needed. #J-18808-Ljbffr Merck
$142.4k - $224.1k
...save and improve lives around the world.The Associate Director, Engineering within Biologics External Manufacturing Technology is... ...partner risks and develop mitigation plans.Develop and execute validation strategies for new and existing products.Provide manufacturing...Full timeContract workTemporary workFor contractorsLocal areaFlexible hours$39.6k - $105.5k
...Under the guidance of Reliability, Maintenance and Utilities Engineers, the Manufacturing and Reliability Engineering Co-op will support... ...submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be...Full timeFor contractorsFixed term contractInternshipLocal areaRelocationVisa sponsorshipFlexible hoursShift work- A growing technology company is seeking a Technical Support Engineer based in Horsham, PA. The role involves troubleshooting, supporting customers with the AVEVA software suite, and requires 3-5 years of experience in a technical support role. Benefits include medical...
- ...maintaining SDLC, GMP, safety, and environmental standards. Responsibilities include validating instruments, implementing change controls, and collaborating with manufacturing, quality, and engineering teams while advancing automation technologies and data analytics #J-18808-...
- ...innovations are built through collaborations. The Process Engineer II is responsible for optimizing and monitoring processes and... ...Familiarity with process scale-up, optimization, cleaning and validation activities preferred. Knowledge of equipment specification...Contract workTemporary workWork experience placementFlexible hours
$32 - $35 per hour
Roth Staffing is seeking a Quality Systems Specialist (Pharmaceutical Validation &Compliance) to support cGMP, FDA regulations, validation protocols, CAPA, RCA, FMEA and SOPs. This 12-month temp-contract role offers an hourly pay rate of $32.00-$35.00 in a regulated pharmaceutical...Hourly payContract workTemporary work- ..., religion, identity, and experience to drive us forward every day.Overview (Scope of Role) The purpose of the Mechanical Project Engineer (Chemical Manufacturing) role is to identify, evaluate and coordinate the design and implementation of capital and expense improvement...
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