22 results (1 new)
Danvers, Massachusetts
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Today
Write clear TMV protocols and reports Create test procedures acceptance criteria and validation plans Interpret test methods specifications and engineering drawings Apply Gage RR (repeatability reproducibility) Ability to select appropriate measurement tools (e.g. verniercalipers micrometers etc.) Collaborate with Engineering
Third Party, Contract
$50 - $55
Remote
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4d ago
Our client seeks an Senior Validation Engineer for a 12 Months project in San Diego, CA . Below is the detailed requirement Title: Senior Validation Engineer (Oracle SCM) Location : San Diego, CA (Remote) Duration:12 Months - UK Shift Time Job Description: Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or related IT discipline or equivalent experience with 12+ Minimum Experience validation is must skills to support NetSuite Validation Eng
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Contract, Third Party
$45 - $50
Cambridge, Massachusetts
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Today
Roles & Responsibilities: We are seeking a seasoned Validation Engineer with 10+ years of experience in medical device or regulated manufacturing environments. Candidates must have strong hands-on expertise in IQ/OQ/PQ protocol development and execution for both new and legacy manufacturing processes and equipment, as well as Test Method Validation (TMV) and Computerized System Validation (CSV) in accordance with GAMP 5. solid working knowledge of regulatory frameworks is essential - specif
Full-time
Remote
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Yesterday
Job Title: Integration Validation Lead Location: Remote/WFH Duration: 9 months+ contract CSV / Validation Lead, with MES experience considered a strong plus. The ideal candidate will have 510 years of relevant experience. Computer Systems Validation (CSV) Lead Key Responsibilities: The selected candidate will support client engagement teams in delivering projects within the Life Sciences domain, including: Leading computer systems validation activities to ensure GxP regulated
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Contract, Third Party
$60 - $65
Remote
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7d ago
<>General SummaryThe Senior Validation Analyst leads strategic validation initiatives to introduce new GxP technologies at Southern Research. From technology assessment and procurement through planning, validation, operational support, and eventual retirement, this role owns validation deliverables and ensures systems remain in a validated state throughout their lifecycle. This position collaborates with the Business, Application Administrators, Information Technology, and internal Quality teams
Full-time
Depends on Experience
Remote
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Yesterday
Sr. CSV Engineer / Sr. Validation Engineer | CSL Behring - Fully Remote | Rate $50-54p/hr to DPR Sr. CSV Engineer / Sr. Validation Engineer 100% Remote 5/4-12/31 Validation Engineer Responsibilities: Lead development of the validation strategy within the first 30 days of onboardingOversee CSA/CSV compliance execution aligned with the customer SDLC and quality proceduresProvide governance, review, and approval of validation lifecycle deliverables (URS, risk assessments, validation plans, specific
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Contract
Depends on Experience
Remote
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2d ago
Bioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote-US) We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the life science Industry. Location:Flexible (Remote) Must overlapat least 5 hours with ESTdaily Job summary We are seeking an experienced Bioinformatics Pipeline Validation Manager with Cancer genomics experience to lead validation efforts for bioinformatics pipelines. This individual will manage a team
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Contract
Depends on Experience
Cambridge, Massachusetts
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Today
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful and usable solutions. From military defense and space exploration to biomedical engineering, lives often depend on the solutions we provide. Our multidisciplinary teams of engineers and scientists work in a collaborative environment that inspires the cross-fertilization of ideas
Full-time
USD 82,300.00 per year
Andover, Massachusetts
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Today
RESPONSIBILITIES: Kforce has a client in need of a Software Quality & Validation Consultant in Andover, MA. Responsibilities: * Lead the implementation of the eQMS system, ensuring it is configured correctly and meets the organization's requirements * Collaborate with quality teams and IT to manage dependencies and ensure seamless integration * Digitize and streamline existing paper-based processes * Attend meetings, engage with consultants, and provide granular-level guidance throughout the im
Third Party, Contract
$55 - $65 hourly
North Reading, Massachusetts
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6d ago
Job Summary: Looking for an experienced IT Validation Lead with strong CSV/CSA and GxP compliance background to support audit readiness and lead validation activities for IT systems in a life sciences environment. Key Responsibilities: Lead Computer System Validation (CSV) activities across IT systemsSupport audit readiness and act as point of contact for auditsPrepare and review validation documents (IQ/OQ/PQ, risk assessments)Ensure compliance with GxP, GAMP 5, FDA regulationsManage validation
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Contract, Third Party
Depends on Experience
Massachusetts
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3d ago
Date Posted: 2026-03-26 Country: United States of America Location: US-MA-ANDOVER-AN3 ~ 354 Lowell St ~ AN3 SUFFOLK BLDG Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance is required prior to start date.Security Clearance Type: DoD Clearance: Secret Security Clearance Status: Ability to obtain INTERIM U.S. government issued security clearance is required prior to start date At Raytheon,
Full-time
USD 86,800.00 per year
Massachusetts
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3d ago
Date Posted: 2026-03-30 Country: United States of America Location: US-MA-ANDOVER-AN3 ~ 354 Lowell St ~ AN3 SUFFOLK BLDG Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance is required prior to start date.Security Clearance Type: DoD Clearance: Secret Security Clearance Status: Ability to obtain INTERIM U.S. government issued security clearance is required prior to start date At RTX, the w
Full-time
USD 68,900.00 per year
Pelham, New Hampshire
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3d ago
Date Posted: 2026-03-25 Country: United States of America Location: US-NH-PELHAM-PE2 ~ 50 Bush Hill Rd ~ BLDG 2 Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance is required prior to start date.Security Clearance Type: DoD Clearance: Secret Security Clearance Status: Ability to obtain INTERIM U.S. government issued security clearance is required prior to start date At Raytheon, the found
Full-time
USD 86,800.00 per year
Wilmington, Massachusetts
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Today
About Analog Devices Analog Devices, Inc. (NASDAQ: ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancements in digitized factories, mobility, and digital healthcare, combat climate change, and reliably connect humans and the world. With revenue of more than $9 billion in FY24 and approximately 24,000 people globally, ADI
Full-time
USD 131,285.00 - 190,108.00 per year
Remote
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Yesterday
Job Title: Quality Control (QC) Validation Scientist Remote Job Summary Takeda is seeking a Quality Control (QC) Validation Scientist to support Analytical Quality Control (AQC) and Microbiology (QCM) activities in a cGMP-regulated environment. The ideal candidate will be responsible for analytical method validation, transfer, troubleshooting, and compliance, ensuring all laboratory operations meet regulatory and quality standards. Candidates with a Microbiology degree or relevant exp
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Contract
Depends on Experience
Massachusetts
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3d ago
Date Posted: 2026-01-06 Country: United States of America Location: MA114: Andover MA 354 Lowell Suffolk 354 Lowell Street Suffolk, Andover, MA, 01810 USA Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance is required prior to start date.Security Clearance: DoD Clearance: Secret At Raytheon, the foundation of everything we do is rooted in our values and a higher calling - to help our natio
Full-time
USD 86,800.00 per year
Boston, Massachusetts
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Today
Job Description: specializing in comprehensive CQV (Commissioning, Qualification, and Validation) and engineering solutions tailored exclusively for the dynamic life science industry. We provide a full spectrum of services, including facilities, utilities, process, and automation engineering, top-tier quality, compliance, and regulatory affairs consulting, and innovative recruiting solutions. Our commitment extends beyond consulting, as we aim to be the next-generation partner providing total ta
Full-time
Remote or Fargo, North Dakota
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Today
Process Validation Specialist / CDMO / Hybrid / Fargo, ND Our client is Large Contract Development and Manufacturing Organization based in Fargo, ND searching for a Process Validation Specialist. The ideal candidate has a strong understanding of the full process validation lifecycle, specifically for biologics products. They are looking for someone who can work independently and manage multiple process validation projects at the same time. This person will be responsible for developing Validatio
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Contract
Boston, Massachusetts
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Today
Responsibilities: Documentation & Deliverables: Develop and author comprehensive validation and quality documentation, including protocols, reports, risk assessments, SOPs, and other project-related materials. Ensure all documentation complies with applicable regulatory standards such as FDA, EMA, GxP, and other relevant guidelines. Review and approve validation documents to confirm alignment with both project objectives and regulatory requirements. Project Management: Lead and oversee multiple
Full-time
Remote or New Jersey
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Today
Job Description: We are seeking a hands-on CSV and Validation Engineer to validate software used with laboratory instruments and lab informatics platforms. The role owns risk-based validation planning and execution aligned to EMA Annex 11 and 21 CFR Part 11, authors audit-ready documentation, and partners with QA/IT/Lab to transition systems to standardized SOPs. Responsibilities: Plan and execute computer system validation using a risk-based CSA approach aligned to GAMP 5. Validate instrument
Full-time
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