Average salary: $132,998 /yearly
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- ...Computer System Validation Specialist 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
- ...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 payContract work
- ...Overview The Validation Specialist II coordinates and implements various activities for compliant and effective support of the Secant Group Validation functions conforming to ISO 13485, internal, and customer requirements. Responsible for performing multiple validation...Suggested
- ...The Validation Specialist will be responsible for designing, executing, and closing validation protocols while ensuring compliance with current Good Manufacturing Practices (cGMPs). This role requires both independent and team-based work, interfacing with various levels...SuggestedFor contractorsWork at office
- ...Electrical Engineer (EE) Hardware Validation Specialist Direct message the job poster from Intelliswift - An LTTS Company Responsibilities Execute comprehensive Hardware Validation testing for new silicon, focusing specifically on Battery Chain ICs and Power Management...SuggestedContract work
$86.94k
...Job Title Validation Specialist. Company Overview Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life‑threatening diseases. Headquartered in Somerset, New Jersey, we develop advanced cell therapies across a diverse array of...SuggestedPermanent employmentFull timeTemporary workFor contractorsLocal areaFlexible hours- ...and portfolio of trusted products like VENDAJE, AmnioWrap2, and others, we empower clinicians to deliver superior outcomes. Validation Specialist/ Tissue Allograph Manufacturing Department: Quality Control Position Summary: We are seeking a detail-oriented Validation Specialist...SuggestedFull timeWork at officeNight shift
$60k - $75k
...Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 360 employees. Your Role Reporting to the Validation Manager, the Validation Specialist is responsible for supporting and executing validation and qualification activities for manufacturing processes,...SuggestedFor contractorsInternshipWork at officeFlexible hoursShift work- ...Job Title: Senior Validation Engineer (IVD / Medical Devices) About the Role We are looking for a Senior Validation Engineer to lead validation activities for manufacturing processes, equipment, test methods, and computerized systems in a regulated IVD / Medical Device...Suggested
- ...alongside professionals who take pride in getting the details right. The Role We are seeking an experienced and highly skilled Validation Specialist to join our growing operations team. In this role, you'll serve as a subject matter expert in validation and qualification...SuggestedFull timeFlexible hours
- ...Join to apply for the Validation Specialist role at PharmEng Technology 2 weeks ago Be among the first 25 applicants Join to apply for the Validation Specialist role at PharmEng Technology Get AI-powered advice on this job and more exclusive features. About The Job Validation...SuggestedFull time
- ...transfers and commercial manufacturing, the office brings industry‑leading Glatt technology to the region. Position Summary The Validation Specialist provides validation support and oversight across one or more of the following areas: 1) NPIx for new processes and equipment...SuggestedWork at office
- ...company which partners with many of the leading employers across the country. Feel free to check us out at Responsibilities Writing validation protocols, coordinating and/or performing validation and writing validation reports to support validation of HVLD, ensuring that...Suggested
- ...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...SuggestedRemote work
- ...Overview The Validation Specialist is responsible for ensuring that our solutions meet the highest standards of quality, accuracy, and compliance. The scope of this job includes validating and verifying that implementations align with client requirements and industry standards...SuggestedWork experience placementWork at office
$55k - $90k
...This role will work from home in the greater Mechanicsburg, PA area and will travel nationally 50-60%. Validation Specialist (US-O) The Validation Specialist role has a national salary range of $55,000 - $90,000. For roles within California the range is $70,3...Casual workRemote workWork from home- ...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...Work at officeImmediate start
$75k - $93.5k
...Overview Validation Specialist II in Camarillo, CA. Build your future at Curia, where our work has the power to save lives. Responsibilities Develops, executes, and reviews validation protocols, including computer system validation, manufacturing equipment qualification...Work experience placement$75 - $80 per hour
...recruiter to learn more. Base pay range $75.00/hr - $80.00/hr Direct message the job poster from Aequor Job Title: Equipment Validation Specialist Location: Portsmouth, NH Duration: 12 Months Job Description: Equipment Validation Specialist exists to ensure all critical...Contract work- ...ISO 13485 . Writing test protocols within KNEAT Gx Knowledge of CQV (Commissioning Qualification and Validation) process. Required Qualifications The Validation Specialist (Contract) will support pharmaceutical and medical device operations by executing and maintaining...Contract workShift workWeekend work
- ...Job Title 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 activities...
- ...Job Title Works collaboratively with the Quality Control and Production Unit to perform routine validation and calibration activities. Assists with onboarding of all new equipment, requalification of existing equipment and all validation activities to include Installation...Work at office
- ...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...Local areaRemote work
- ...Job Description Job Description Validation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device IT & Human Resources disciplines in New Jersey. The Validation Specialist performs validation...Work at officeFlexible hours
- ...products Tuition Assistance Life & Disability Insurance Employee Referral Awards The Position Primary responsibility is to provide/lead validation services required for the successful delivery of IT & Automation projects. Relationships Reports to Senior Project Manager, Site...For contractorsWork experience placementLocal areaShift work
- ...Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Computer System Validation Specialist. Responsibilities: Performs and leads computer system validation projects related to authoring and executing...
- ...Senior GxP Systems & Validation Specialist (Biotechnology) San Mateo, United States | Posted on 05/30/2026 Our client, a world‑leader in life sciences and biotechnology, is looking for a “Senior GxP Systems & Validation Specialist” based out of Foster City, CA (Hybrid)...Long term contract
$118k - $162.8k
...Job Description This individual will provide thought‑leadership, expertise, and management of managed validation services to the IT Validation & Compliance infrastructure in a Contract Development and Manufacturing Organization (CDMO) setting. The role is responsible...Contract work- ...Computer Systems Validation Specialist III Location: 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...Relocation package
- ...ensuring better health and well-being for patients around the world. The Impact You Will Make The Computer System Validation (CSV) Specialist is responsible for ensuring that all GxP computer systems used in pharmaceutical manufacturing environments are validated...Local area


