Average salary: $132,998 /yearly
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- ...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
- Summary : Support cleaning validation activities, protocol execution, sampling, and documentation. Perform temperature mapping and requalification of controlled temperature units. Execute IQ/OQ/PQ, requalification, and periodic review for GMP equipment and utilities. Support...Suggested
$128.47k - $208.77k
...Caterpillar Autonomous Program and plays a critical role in delivering high‑quality, technology‑ready autonomous platforms. The Autonomy Validation Lead will drive System Integration and Validation (SI&V) activities, primarily conducted in laboratory environments and closely...SuggestedFull timePart timeWork at officeRemote workRelocationRelocation packageFlexible hours- Job Description: This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area. This role will be supporting validation leads to help ensure the required...Suggested
- ...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...SuggestedWork at officeImmediate start
- Responsibilities:Lead validation activities for Labware LIMS 8 implementationAuthor and review IQ/OQ/PQ, RTM, and validation documentationEnsure compliance with GXP, CSV, and regulatory standardsSupport audits, inspections, and validation testing activities.Required Skills...Suggested
- ...worldwide. For more details, please visit : Job TitleEXPANSION Validation SpecialistJob DescriptionBusiness: Pharma SolutionsDepartment:... ...to the Validation Supervisor, the Validation Specialist executes validation and qualification protocols of manufacturing...SuggestedContract workWork at officeWorldwide
- ...your potential? Join Team Novo Nordisk and help us make what matters.The PositionPlan, manage & perform low to moderately complex validation projects and activities. Support engineers with writing change requests and conducting/writing deviation investigations. Support...SuggestedWork at officeLocal area
- ..., Canada, and South America. Professional Summary Experienced professional in laboratory protocol review, document revision, and validation of laboratory computerized systems (CSV) and SOPs. Skilled in LIMS and Empower, with extensive experience in laboratory instrument...Suggested
Mentor Technical Group
Bradenton, FL2 days ago - ...GMP Equipment Validation Specialist- ICON - Lenexa KS Title: GMP Equipment Validation Specialist Location: Lenexa, KS What you will do As a GMP Equipment Validation Specialist at ICON you will be responsible for the ongoing qualification of equipment and controlled environments...SuggestedRemote workFlexible hours
ICON
Lenexa, KS2 days ago - ...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
Rees Scientific
Boston, MA21 hours ago - A technology company focused on AI training is seeking a Sell-Side Analyst. This role allows for remote work and flexibility in scheduling, making it suitable for both part-time and full-time contributions. The ideal candidate has a strong background in finance, with advanced...SuggestedHourly payFull timePart timeRemote work
DataAnnotation
Wausau, WI2 days ago - ...Payrate: $45 to $57/hr on W2 (depending on experience) Description: The Validation Specialist (Contract) will support pharmaceutical and medical device operations by executing and maintaining compliant validation activities using Kneat Gx as the electronic validation lifecycle...SuggestedContract workShift workWeekend work
Integration International Inc
Marion, NC2 days ago $96k - $120k
...Lyell Immunopharma, Inc. is seeking a Quality Assurance Specialist to oversee compliance in a cell therapy manufacturing environment. The role involves providing QA oversight for Facility, Equipment, Utility, and Computer System programs, ensuring adherence to GMP requirements...SuggestedLyell Immunopharma, Inc.
Bothell, WA2 days ago$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...SuggestedFull timeTemporary workPart timeCasual workWork at officeLocal areaImmediate startFlexible hours- Job Description: We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. The ideal candidate will be responsible for planning, executing, reviewing, and approving validation documentation...
- ..., engineers, interior designers, consultants, sustainability specialists, and technologists are passionate about the power of design.... ...and throughout the building lifecycle. As a Commissioning / Validation Specialist, you will support the delivery of high-quality commissioning...Full timeTemporary workPart timeFor contractorsCasual workWork at officeLocal areaFlexible hours
- Computer Systems Validation (CSV) SpecialistLocation: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families.The Computer Systems Validation (CSV) Specialist helps to lead team members to assess new and changing computer systems to...Full timeRelocation package
- ...realize your potential? Join Team Novo Nordisk and help us make what matters.The PositionPrimary responsibility is to provide/lead validation services required for the successful delivery of IT & Automation projects.RelationshipsReports to Senior Project Manager, Site...Work experience placementLocal areaShift work
- ...Assurance team is expanding, and we're looking for a process validation professional with hands-on experience and a strong command of... ...validation life cycle.The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance...Full timeH1bVisa sponsorshipWork visa
- ...dynamic healthcare environment dedicated to accuracy, compliance, and quality patient care.DutiesReview NLP-generated HCC coding output.Validate assigned codes against available documentation.Identify unsupported, inaccurate, or missing codes.Make corrections in the platform...Flexible hours
$105.28k - $150.4k
Role Description The Computer System Validation (CSV) Lead is responsible for developing, executing, and maintaining the validation strategy for GxP-regulated computerized systems supporting manufacturing, laboratory, and quality operations. This role ensures that all...Full timeAstellas Pharma
Remote4 days ago- ...engagement – all enabling you to make a meaningful impact on patient health. Position Summary As a MSAT Senior Product and Process Validation Specialist, you will develop, validate, optimize, and maintain robust manufacturing processes in our vaccine production facility. Your...Local areaRemote work
GlaxoSmithKline
Marietta, PA2 days ago $40 per hour
A leading AI development company is looking for experienced quantitative professionals to evaluate AI-generated work and solve complex problems. This remote role allows you to choose your projects and schedule, offering competitive pay starting at $40 USD per hour. Candidates...Hourly payRemote workDataAnnotation
New York, NY4 days ago- ...A leading insurance firm is looking for a Model Validation Specialist to oversee the validation of AI and ML models. This role involves close collaboration with technical and business teams to ensure compliance and quality. Candidates should have an advanced degree in...Work at officeRemote work
New York Life
New York, NY4 days ago - Responsibilities: Client is seeking validation consultants to support a 9-month minimum onsite project in South Carolina. The consultants will support validation execution and gap assessments tied to equipment qualification, tank qualification, mixing studies, smoke studies...
- ...design quality and coverage.Apply expertise in high-speed I/O protocols, IP verification, and formal verification technologies to validate next-generation semiconductor designs.Drive adoption of cutting-edge formal verification and automation techniques to improve verification...
- The primary responsibility of this position entails executing the silicon validation and characterization of cutting edge high performance highspeed low power CMOS D2D and SERDES silicon interface following industry best practicesBring up validate and characterize highspeed...
- A brief overviewThe Quality Engineer (QE) / Validation fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of equipment, facilities, utilities. This position will work in close cooperation...
- Summary : We are seeking an experienced Validation Engineer to support pharmaceutical manufacturing and quality operations in Washington. The ideal candidate will have hands-on experience in equipment, process, cleaning, and computerized system validation within a GMP-...
