Validation Specialist- III
Artech Information Systems LLC
Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• QC Instrumentation Services is responsible for the management and implementation of the Laboratory Equipment Qualification system. • It's goal to efficiently specify/source laboratory equipment and execute qualifications in a timely manner to enable QC Microbiology and QC Chemistry departments to execute their functions using equipment which meets their needs and intended use. • This position is responsible for qualifying analytical and microbiological testing instrumentation for the company. • These are some of the responsibilities: • Coordinate activities relating to the qualification, calibration and maintenance of laboratory equipment and related systems. • Coordinate the purchase, commissioning and introduction to service of new equipment.• Establish and maintain Equipment History Files (EHF) for QC laboratory equipment. • Be the contact point for instrumentation issues and provide training and troubleshooting support to the laboratory on new or existing instrumentation. • Coordinate all services provided by vendors, ensuring vendors meet all site requirements. Schedule/plan/execute validation activities and preventive maintenance of laboratory equipment. Skills:• Demonstrated scientific technical writing ability. • Knowledge of USP 1058 and GAMP methodology. • Knowledge of 21CFR Parts 11, 210, 211, 600 and 610. • Experience with Empower and LIMS systems. • Previous hands on experience performing laboratory equipment qualification. • Proficient in Outlook and Microsoft Word and Excel and lab based data management systems. • Ability to gown and enter laboratory • May require off shift work to support activities • Ability to gown and enter laboratory • May require off shift work to support activities QualificationsEducation: Bachelor's Degree in Chemistry, Life Sciences, or Engineering discipline and 5 years of Industry relevant experience Or Master's Degree in Chemistry, Life Sciences, or Engineering discipline and 3 years of Industry relevant experience Minimum of 3 years of experience with analytical testing in a laboratory setting, such as HPLC, GC, Ion Chromatography, TOC, UV-Vis, ELISA.Additional InformationFor more information, please contact:Sneha ShrivastavaTechnical Recruiter (Clinical/Scientific)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: View phone number on click.appcast.io | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: ResearchExperience level: Mid-Senior LevelIndustry: Pharmaceuticals
- ...team members united by a common belief: to use the power of business to build a better world.Job Description:Job SummaryThe Validation Engineer III will serve as a key member of the validation team, providing expert-level support to ensure facility equipment, utilities,...SuggestedFull timeFor contractorsWork at office
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$101k - $178.14k
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...Learn more at We are hiring for Senior Robotics Verification & Validation (V&V) Engineering Manager in a hybrid role to be based out of Raynham... ..., Jama, Polarion).Preferred• Experience with Class II or Class III medical devices is preferred.• Knowledge of embedded systems,...SuggestedFull timeLocal areaImmediate start- ...System Validation Specialist As a System Validation Specialist, you have hands on experience with installing, troubleshooting, repairing, calibrating, and inspecting monitoring equipment used in healthcare facilities. The System Validation Specialist will maintain a...SuggestedLocal areaRemote work
$107.1k - $160.7k
..., engineers, interior designers, consultants, sustainability specialists, and technologists are passionate about the power of design.... ...that support and enhance our communities. The Commissioning and Validation role provides crucial services to confirm equipment and...Full timeTemporary workPart timeCasual workWork at officeLocal areaImmediate startFlexible hours$92k - $148.35k
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...Secure. What You’ll DoAs a Senior RF Test Engineer, you will be a key technical leader responsible for RF product development and validation at SimpliSafe. You help design and build SimpliSafe’s RF capabilities in our goal to have the best-in-class wireless connectivity...Work at office$100.05k - $156.49k
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...Description COMPANY: Thermo Fisher Scientific, Inc. LOCATION: 5 Commerce Blvd Plainville, MA 02762 TITLE: Automation Engineer III HOURS: Monday to Friday, 8:00 am to 5:00 pm DUTIES: Responsible for supporting Thermo Fisher VVS facilities in Plainville, Ma...Temporary workWork at officeLocal areaMonday to Friday$150k - $250k
...comprehensive coverageCollaborate with design engineers to understand design intent and provide feedbackPerform RTL verification and validate key components including memory subsystems and interconnect architecturesContribute to post-silicon validation efforts to ensure...- ...done. We’re obsessed with how it will be done.Key ResponsibilitiesCQV Execution & Safety- Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety- Deliver C&Q activities in alignment with project schedules- Track and report...Full timeFor contractorsWorldwide
$82.3k - $220k
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Anduril Industries is a defense technology company with a mission to transform U.S. and allied military capabilities with advanced technology. By bringing the expertise, technology, and business model of the 21st century’s most innovative companies to the defense industry...Full timeWork experience placementImmediate startFlexible hours- ...across multi-vendor platformsStrong troubleshooting and diagnostics capabilities across complex analytical systemsExperience with GxP validation, equipment qualification, and SOP developmentCore SkillsAbility to design and implement service processes independentlyStrong...
- Job Description: The Quality Engineering and Validation Consultant is recognized as an expert internally in the principles and application of quality assurance and compliance. This position coordinates GMP activities in support of clinical and commercial Drug Product...Work experience placementMonday to Friday
$82.3k - $220k
...fertilization of ideas necessary for true innovation. For more information about Draper, visit .Job Description Summary:A Senior Analog ASIC Validation Engineer specifies, designs, verifies, tests and validates on the bench, and documents Application-Specific Integrated Circuits....Full timeWork at officeLocal area$107.5k - $204.5k
Job ID: 01847979Posted: Posted 30+ Days AgoStart Date: 2026-05-26Location: US-MA-MARLBOROUGH-MA2 ~ 1001 Boston Post Rd ~ BLDG 2Country: United States of AmericaTime Type: Full timeDate Posted:2026-05-26Country:United States of AmericaLocation:US-MA-MARLBOROUGH-MA2 ~ 100...Temporary workWork experience placementWork at officeRemote workRelocationFlexible hours$75k - $245k
...of safety critical systems to coordinate V&V guidance system software. Lead the technical effort of independently verifying and validating safety critical software. Must understand V&V process and how it fits into system lifecycle. Staff must be able to independently...Full timeLocal area
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