Average salary: $132,998 /yearly
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- ...Position Summary We are seeking a detail-oriented Validation Specialist to support validation and qualification activities within a pharmaceutical manufacturing environment. This individual will help ensure that manufacturing equipment, utilities, facilities, computerized...SuggestedFull timeWork at office
- ...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
- ...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
- ...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-ID33111878Reference26-01830Summary :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...Suggested
- Job-ID32495586Reference26-01079Remote50% RemoteResponsibilities: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...Suggested
- Job-ID32892617Reference26-01524 Requirements: 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...Suggested
- Job-ID32981060Reference26-01708Job 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...Suggested
- ...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...Suggested
- ...Validation Specialist Linde Gas & Equipment Inc. Morrisville, PA, United States | req33223 What You Will Enjoy Doing Manage the overall validation program for all LG&E operations and systems Support all locations with executing validation protocols Interface...Suggested
- ...Job Title Key Responsibilities Perform commissioning, qualification, validation, and maintenance activities within the facility. Oversee multiple CQV projects, providing updates and coordinating with internal teams and external vendors. Lead and support...SuggestedWork at office
- ...Responsibilities: Lead validation activities for Labware LIMS 8 implementation Author and review IQ/OQ/PQ, RTM, and validation documentation Ensure compliance with GXP, CSV, and regulatory standards Support audits, inspections, and validation testing...Suggested
- ...Functional Requirements (FRS), Configuration/Design Specifications, Risk Assessments, Requirement Traceability Matrices (RTMs), Validation Plans (VMP), Test Plans, and Validation Summary Reports (VSR). Execute validation lifecycle documents including Installation Qualification...SuggestedContract work
- ...The Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems. Primary responsibilities include: qualification of laboratory instruments, setup of computers and instruments, troubleshooting...SuggestedWork experience placement
- ...Job Description: ~ We are seeking an experienced Validation Specialist to support validation activities for Syringe Assembly Machines (SAM) in a GMP-compliant pharmaceutical environment. The ideal candidate will possess a strong understanding of the validation lifecycle...SuggestedHourly pay
$60.5k - $95.7k
...Summary The CIP Validation Specialist assists the Validation team with ensuring that all automated CIP circuits and CIP stations are operating efficiently and effectively. The Validation Specialist is responsible for assisting with the validation of all the key parameters...Full timeLocal areaImmediate startFlexible hoursNight shift- ...Job 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 Sciences. Hands-on experience...
- ...JOB TITLE: Validaton Specialist Lead JOB LOCATION: Milford, Ma Must be onsite WAGE RANGE*: 45 - 50/ hour JOB NUMBER:... ...run and execute CV Protocols. Proven work experience as a Validation Engineer or similar role. Strong knowledge of validation...Hourly payTemporary workWork experience placementLocal areaFlexible hours
- ...Title: Computer Validation Specialist - Pharma Industry Experience : 6+ years Location: Plantation, Florida Job Summary: The Computer Validation Specialist will be responsible for ensuring that computerized systems remain compliant with applicable regulatory...Full timeFor contractors
- ...Computer System Validation (CSV) Specialist – Consultant Location: Remote with preference for 1–2 days onsite per week in the greater Cincinnati, Ohio area. Schedule: Part-time, approximately 20 hours per week Duration: 3 months Start: ASAP Position Overview...Part timeImmediate startRemote work2 days per week1 day per week
$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- ...the responsibilities listed below, this position is also responsible for performing initial testing and setup procedures (e.g., validation, verification, calibration, sensitivity studies) for new or replaced instruments; supporting assay development; and contributing...Local area
- Job-ID32940527Reference26-01625 Requirements: Experience supporting validation activities, including equipment, process, facility, computerized systems, and documentation review. Preferred experience in high-speed aseptic filling operations and sterile manufacturing environments...
- Computer Systems Validation Specialist IIILocation: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.The Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to...Full timeRelocation package
$145k - $160k
...available cell therapy on demand, more reliably, and at greater scale to more patients. About the role:The Senior Qualification / Validation Specialist develops, implements, and manages equipment qualification and validation strategies and activities supporting Allogene...Full timeLocal area- Job-ID32854161Reference26-01446 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 Specialist Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our...Temporary workCasual workInternshipMonday to FridayFlexible hours
$31.4 - $34.4 per hour
We are seeking an MS&T Process Validation Specialist to support process validation activities at a cell therapy manufacturing facility in Devens, MA. This role focuses on supporting aseptic process simulations and validations (APS/APV), process lifecycle management changes...Hourly payContract workFor contractorsVisa sponsorshipMonday to Friday- A national recruiting firm is seeking an individual to perform audits and validation for financial clients in Los Angeles. Responsibilities include reviewing compliance with management control assessments, compiling reports for senior management, and managing ongoing MCA...Work at office
- Kelly® Engineering is seeking Validation Specialist for contract position at manufacturing client in Arroyo, Puerto Rico. If you’re passionate about bringing the latest professional discoveries to life and are ready to take the next step in your career, trust The Experts...Contract workTemporary workLocal area


