Validation Specialist II
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 DescriptionThe consultant will use his/her knowledge of FDA cGMP and related regulations and guidelines, and specific knowledge of computer system validation (CSV) methodologies and principles to perform CSV on a variety of laboratory systems in the QC department at the Canton site .The successful candidate must be an independent performer with significant experience in a cGMP environment, and will work with minimal supervision.Skills:At least 2-4 years of Computer System Validation experience in a laboratory environment. Past experience writing, reviewing and executing computer validation documentation (Validation Plan, IQ, OQ, PQ, DSN, summary report).An excellent understanding of CFR-Part 11 Compliance for Electronic Data Systems.A good understanding of laboratory instruments such as HPLC's, TOC, UV-Spectrophotometers , FT-IR's among others.A good understanding of the Windows OS (XP/Windows7) including file hierarchies, Data Structures, Networking and VBS or other basic scripting languages. A basic understanding of Microsoft SQL is a plus.QualificationsBS in Chemistry/Biology/Computer Science or a related area with significant experience in laboratory instrumentation in a cGMP environment.Additional InformationBest Regards,Akriti GuptaAssociate Recruiter(Scientific & Clinical Division)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: Information TechnologyExperience level: AssociateIndustry: Pharmaceuticals
$145.9k - $234.2k
...the Director, Global Drug Product Automation, the Sr. Engineer II, Drug Product will serve as a technical leader responsible for defining... ...change control, configuration management, system lifecycle, and validation practices are incorporated into automation-related changes in...SuggestedPermanent employmentFull timeWork at officeWork from home$120k - $160k
...bodies and daily lives.WHOOP is seeking a Manufacturing Engineer II with a focus on New Product Introduction (NPI) to help bring... ...Engineering, Supply Chain, and our manufacturing partners to develop, validate, and optimize manufacturing processes that deliver high-quality...SuggestedFull timeWork at officeRelocation$116k - $162.75k
...making our One Team culture thrive. Join us as Senior Engineer II, Manufacturing Science and Technology, and you’ll be part of a... ...automation control modules, batch records, process control and validation strategies. Partner closely with stakeholders to ensure...SuggestedWork experience placementLocal area- ...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. •...SuggestedWork at officeImmediate startShift work
- Job-ID32981060Reference26-01708Job summary:We are seeking an experienced Validation Specialist to support validation activities in a GMP-regulated environment.Roles and Responsibilities:10 years of experience in Validation within Pharma, Biotech, or Life SciencesHands-on...Suggested
$84k - $134.1k
The Role: In this role, you will play a crucial part of our manufacturing operations, supporting the operation of our cutting-edge GxP manufacturing systems. These systems include, but are not limited to, Aveva System Platform, Rockell Automation ControlLogix, DeltaV, Syncade...Permanent employmentFull timeApprenticeshipWork at officeWorldwideShift work$148.5k - $237.6k
...grow as you work hard for a mission that matters at a company where you matter.Your Impact As a Senior Security Operations Engineer II, you will play a key role in building secure, reliable, and developer-friendly infrastructure that enables teams to move quickly without...Work experience placementWork at officeRemote work- ...Role: Process Engineer II supporting cGMP manufacturing of autologous cell therapies within the MSAT team, focusing on technology transfer, process support, and ongoing commercial production. Responsibilities: lead technical support for GMP runs, conduct investigations...
- ...Job summary: We are seeking an experienced Validation Specialist to support validation activities in a GMP-regulated environment. The ideal candidate will have strong hands-on expertise in equipment, facility, utility, and/or process validation, including IQ, OQ,...
- At Materion, everyone is included, respected and offered opportunity to grow. Join us! POSITION SUMMARY This position is key in driving manufacturing process improvements with the goal of optimizing safety, quality, and efficiency. This includes teaming with supervisors...Permanent employmentFor contractorsLocal area
$98k - $182k
Job Description: Established nearly two centuries ago, FM is a leading mutual insurance company whose capital, scientific research capability and engineering expertise are solely dedicated to property risk management and the resilience of its policyholder-owners. These...Full timeFlexible hours$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$117k - $201.25k
...more at We are hiring for Navigation Systems Verification & Validation (V&V) Engineering Manager in a hybrid role to be based out of Raynham... ...communication skills. Preferred Experience with Class II or Class III medical devices is preferred. Knowledge of...Local areaImmediate start$68.9k - $131.1k
Job ID: 01880599Posted: Posted YesterdayStart Date: 2026-10-08Location: US-MA-MARLBOROUGH-MA3 ~ 1001 Boston Post Rd ~ BLDG 3Country: United States of AmericaTime Type: Full timeDate Posted:2026-10-08 Country:United States of America Location:US-MA-MARLBOROUGH-MA3 ~ 10...Temporary workWork experience placementInterim roleWork at officeLocal areaRemote workRelocationFlexible hours- The Computer System Validation (CSV) Specialist ensures computerized systems are validated, maintained, and operated in compliance with applicable regulatory requirements and industry best practices. The role serves as a subject matter expert in CSV, FDA 21 CFR Part 11,...
$130k - $140k
...Engineer II Demand Tech (Scala, Rust) Boston, MA New York City, NY Hybrid Schedule (M/F remote, T/W/TH in-office) At Magnite, we cultivate an environment of continuous growth and collaboration. Our work impacts what millions of people read, watch, and buy, and we’re looking...Work experience placementWork at officeLocal areaRemote workMonday to Friday$68.9k - $131.1k
...embarking on a journey to shape the future of aerospace technology.Our Connected Aviation group is thrilled to offer a Systems Engineer II role within our Air Traffic Solutions (ATS) team in Marlborough, MA. As part of the ATS team, you'll be instrumental in developing...Contract workTemporary workWork experience placementStart working todayWork at officeRemote workWorldwideRelocationFlexible hours$110k - $150k
...age; we serve the aspiring!WHOOP is hiring an Electrical Engineer II to help accelerate the development of the next generation of... ...reliability, and overall system performanceSupport design verification, validation, and new product introduction (NPI), partnering with...Full timeContract workWork at officeRelocation- Job-ID32864156Reference26-01463 Job Summary: We are seeking an experienced Validation Engineer to support system-level Verification & Validation (V&V) activities for medical device products. The role involves planning and executing V&V activities, developing and executing...
$74.8k - $130.9k
...your full potential. Unleash your talent and redefine what’s possible.Job Description:Parsons is looking for a Civil/Highway Engineer II to join our team! In this role, you will have the opportunity to design streets, highways, interchanges, railroad sites, and other...Full timeContract workWork experience placementFor subcontractorWork at officeFlexible hours$110k - $150k
...understanding of their bodies and daily lives. As a Mechanical Engineer II on WHOOP’s Continuous Improvement Team, you will play a key role... ...with global suppliers and contract manufacturers to execute validation builds, with a focus on high-quality deliverables, effective...Full timeContract workWork at officeRelocation- ...or Scientific discipline· 5+ years of work experience in medical device industry· Experience conducting Process Verifications / Validations· Experience conducting Design and/or Process Failure Modes Effects and Analysis· Excellent problem solving and decision-making skills...Work experience placement
- ...,000 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...Full timeFor contractorsWork at office
- Job-ID33196738Reference26-01934 Job Summary We are seeking a Medical Device Quality / CSV Validation Engineer to support quality system compliance, CAPA remediation, spreadsheet validation, and computer system/software validation activities within a regulated medical device...Local area
$124k - $186k
...The engineer provides day-to-day technical direction to contractors and works closely with Manufacturing, Engineering, Quality, Validation, and vendors.Key ResponsibilitiesSupport automation upgrades and modifications for data integrity and reliability improvements for...Full timeFor contractorsSummer workFlexible hours- ...Job Summary and Objective: The Mechanical Engineer II will collaborate with team members to design and refine cutting-edge medical devices, contributing to product testing, validation, and optimization. Working closely with management, quality assurance, supply chain...Temporary workWork experience placementWork at office
$71.3k - $97.75k
...standards of care. Job Summary This Supplier Quality Engineer II role serves as a key quality representative supporting contract... ..., supplier change control, quality agreement management, and validation activities while ensuring compliance with FDA 21 CFR Part 820, ISO...Contract workTemporary workWork experience placementWork at office$96k - $153k
...we love it.Your Opportunity:Chewy is seeking a Hardware Engineer II to join our Fulfillment Center Design Engineering Team. In this... ...cost.Partner with vendors and internal teams to scope, design, and validate new fulfillment technologies such as conveyance, sortation, and...Work experience placementLocal areaFlexible hours$78k - $100k
...Job Description Job Description Job Title: Engineer II Department: Operations Engineering Reports To: Divisional Information Security Officer Revision Date: 08/7/2026 FLSA: Exempt Location: Stoughton, MA Preferred Level: T2 Rate of Pay: $...Work at officeRemote work$74k - $118.4k
The Role We are seeking a highly skilled and motivated Individual, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support drug product development...Permanent employmentWork from home
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