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
- ...Validation Specialist 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
- ...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...Suggested
- ...Job Title Roles & Responsibilities: 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
- ...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
- ...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
- ...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
- ...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
$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...SuggestedFull 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...Suggested
- ...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...SuggestedHourly 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...SuggestedFull 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...SuggestedPart 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- Job-ID32810458Reference26-01386 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
$93.5k
JOB TITLE & Employer Name: Validation Specialist for Harvard Bioscience, Inc. LOCATION: 119-14th Street NW., Suite 100, St. Paul, Minnesota 55112. JOB DUTIES: Develop and implement validation documentation that include Standard Operating Procedures, Master Validation...Remote work- Working title: Validations Specialist I Class title: Program Specialist III Posting No.: 1005-27 Opening Date: 10/08/2026 Closing Date: 10/22/2026 Location: Bush Building, 1801 Congress Ave., Austin, TX 78701 Class Code: 1572 FLSA: Non-Exempt Salary Group/Salary...Work at office
- Penn Life Sciences, Inc. is seeking a Validation Associate to support commissioning, qualification, validation, requalification, and documentation activities within a sterile injectable manufacturing facility. You will work cross-functionally with Manufacturing, QA, Engineering...
$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
$25 - $39.38 per hour
Labcorp is seeking an Assay Validation Specialist in Torrance, CA. This role focuses on assay validation, verification, and laboratory method development. Responsibilities include executing validation experiments, developing validation plans, and maintaining compliance...$560 - $800 per day
About the opportunity Validation Specialist positions in this area could sit within quality assurance and product development teams working to bring validated solutions to market. The work could involve partnering across engineering, quality and manufacturing to design...Full timeContract workFlexible hours$25 - $39.38 per hour
Overview Labcorp is seeking a Assay Validation Specialist to join our team in Torrance, CA. Work Schedule: Monday-Friday 9am-5:30pm. This position focuses on assay validation, verification, and laboratory method development. The role supports validation projects from planning...Temporary workCasual workInternshipMonday to FridayFlexible hours- ...Job Description Job Description Full Time Contract Role: Validation Specialist Location: Barceloneta, PR (Onsite) Length of Contract: 6 months Position Description The Validation Specialist supports commissioning and qualification (C&Q) activities...Full timeContract work
- ...Quality Investigator Location: Raleigh, NC 27615 Pay : $55-60/HR on W2 Monday to Friday, Hybrid, 3 days in office The Validation Specialist, Regulatory is responsible for implementing GxP computerized systems for the R&D IT department. A successful candidate will...Work at officeMonday to Friday
- ...Labcorp seeks a Validation Specialist for its Flow Cytometry team in Brentwood, Tennessee. The role involves executing validation projects, performing laboratory bench work, maintaining flow cytometry equipment, and generating technical documentation while ensuring compliance...




