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Healthcare
› Computer System Validation
Computer System Validation
328 open positions
Validation Specialist 3
Pciservices
Mississauga, CAN, CA
$75k–$75k
9d
Own high-risk validation projects for biopharma clients, ensuring compliance with cGMP/GAMP/21CFR standards and delivering validated processes for product/system launches.
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Validavimo inžinierius (-ė) | Įrangos ir sistemų kvalifikavimas – Vilnius
Thermofisher
Vilnius, Lithuania
$26k–$26k
10d
Plan, execute, and control equipment and system qualification activities per ISO 13485 and IVDR requirements; oversee third-party vendor work.
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6518 - Service Order CQV Engineer / Validation Engineer
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Verista
Indianapolis, IN, US
10d
Provide technical CQV (commissioning, qualification, and verification) expertise on large capital projects involving new or modified equipment, facilities, and utilities in the life sciences industry.
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6097 - Senior CQV Engineer / Senior Validation Engineer
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Verista
Bloomington, IN, US
10d
Provide engineering and CQV support for the implementation, modification, commissioning, and qualification of manufacturing equipment and systems in regulated environments.
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CSV Validavimo Inžinierius (-ė) | Kompiuterizuotos ir automatizuotos sistemos – Vilnius
Thermofisher
Vilnius, Lithuania
$26k–$26k
10d
CSV validation engineer for computerized and automated systems in manufacturing, laboratory, quality, and technical operations environments.
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Senior Specialist, Validation Engineer II
Bristolmyerssquibb
Devens - MA - US
$93k–$93k
11d
Qualifies and validates manufacturing, laboratory equipment, facilities, and utilities to ensure they remain in a qualified state for biologics/cell therapy production.
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CQV Engineer
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Amaris Act Pte. Ltd.
Tanjong Pagar, S00, SG
11d
Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems in a GMP environment.
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Consultant - Business Consulting Risk - TMT - CNS - RISK - DIGITAL RISK - Mumbai
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EY
MH, IN
11d
Consultant specializing in Computer System Validation (CSV) for Life Sciences clients to ensure compliance with regulatory requirements and internal procedures.
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QA Granada Tech Center- Intern - ANS
Abbott
Spain - Granada
11d
Support the quality system and validation area at the Tech Center by managing validation documentation, protocols, reports, and data collection.
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Sr Validation Specialist (LIMS)
Thermofisher
Remote
11d
Provide technical expertise for LIMS products and computer system validation (CSV) in regulated environments.
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Ingeniero de Calificaciones (Temporal - 12 meses)
Gsknch
Argentina - Buenos Aires Province - Buenos Aires
11d
Execute equipment, system, and facility qualification activities; support engineering projects for new equipment and technology integration; manage requalification and maintenance history analysis.
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Validation Engineer
Freseniusglobal
Grand Island, NY
$61k–$61k
11d
Validates and revalidates pharmaceutical products, equipment, and systems to ensure compliance with cGMPs and industry standards.
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Senior Specialist, Validation Engineer - CSV
Bristolmyerssquibb
Devens - MA - US
$93k–$93k
11d
Qualify and validate Process Control Systems (DeltaV) and Manufacturing Execution Systems (MES) for clinical and commercial biologics manufacturing facilities.
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Sr. Automation Engineering
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Juncos, PR, US
12d
Sr. Automation Engineer supporting validation services for pharmaceutical and regulated industries, ensuring utility systems and process maintenance comply with FDA and industry standards.
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Validation Engineer Sterilization (MS&T)
Galderma
Uppsala
12d
Subject matter expert for sterilization processes, specifically leading validation and qualification of autoclaves and VHP decontamination systems to ensure compliance and patient safety.
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Qualification and Validation Specialist
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Sanofi
Toluca, MEX, MX
12d
Guardian of laboratory technical integrity, leading qualification and validation of equipment and instruments to ensure data traceability and regulatory compliance.
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Computer System Validation Engineer (Senior)
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Integrix Solutions Pte. Ltd.
Singapore, S00, SG
12d
Create, review, or approve validation deliverables for GMP computerized systems in pharmaceutical manufacturing, including User Requirements Specifications, Design Reviews, Criticality assessments, Validation protocols (IQ, OQ, PQ), and Incident/deviation…
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Intern - IT Quality and Compliance
Labcorp
Madison WI
12d
Support IT Quality and Compliance activities, specifically Computer System Validation (CSV) and periodic reviews for Drug Development Labs.
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Prozessingenieur Validierung & Qualifizierung (m/w/d) Arbeitsort: Lorsch
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Prisman GMBH
Mannheim, BW, DE
12d
Develop and execute validation and qualification strategies for medical devices and hygiene products throughout the product lifecycle.
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Validation Engineer
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Coalesce Management Consulting
Singapore, S00, SG
12d
Develop and execute qualification documentation and testing for laboratory equipment to ensure compliance and readiness for routine operation in GMP-regulated environments.
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Computer System Validation (CSV) Engineer
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Xot Solutions Pte. Ltd.
Singapore, S00, SG
12d
Subject matter expert ensuring GxP computerized systems remain validated throughout their operational life, focusing on Life Cycle Management (LCM) projects.
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Staff Validation Engineer, Process and Cleaning
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Thermo Fisher Scientific
Greenville, NC, US
14d
Ensuring manufacturing processes and cleaning procedures are validated, compliant, and capable of consistently delivering high-quality products in a sterile/aseptic environment.
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Validation Lead Radiopharmacies
Gehc
Eindhoven
15d
Establishing and implementing a central validation and maintenance strategy for HVAC, lab, and QC equipment across three radiopharmacy locations to ensure GMP-compliant production readiness.
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ANALISTA DE VALIDAÇÃO DE SISTEMAS COMPUTADORIZADOS PLENO (GMP Quality Consulting)
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Jobbol
Osasco, SP, BR
15d
Design and execute computerized system validation protocols (URS, FS, DS, IQ, OQ, PQ) and perform risk analysis and system classification per GAMP 5.
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Sr. Computer Systems Validation Analyst
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Katalyst Healthcares & Life Sciences
Foster City, CA, US
15d
Planning, leading, and executing Computer Systems Validation (CSV) for SCADA, PLC, and process control systems in GxP-regulated environments.
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Projektmanager Qualifizierung & Validierung Health (m/w/d)
Marktredwitz, BAYERN
15d
Leading industrialization projects and managing qualification/validation activities for medical devices, manufacturing processes, and computerized systems.
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Sr Business Systems Analyst
Dexcom
Penang, Malaysia
15d
Subject Matter Expert for validation and compliance of Enterprise and Manufacturing Systems (MES, ERP, QMS, SCADA, PLC) in a medical device environment.
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Sr. Associate Validation Engineer
McKesson
USA, KY, Shepherdsville
$66k–$66k
16d
Ensuring pharmaceutical storage, distribution, and transportation systems remain validated and compliant with GMP/GDP regulations through qualification, validation, and calibration activities.
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Principal/Senior Principal Validation Engineer
Roche
Holly Springs
$95k–$95k
16d
Establishing and executing lifecycle validation strategies (IQ/OQ/PQ/PPQ) for high-speed pre-filled syringe assembly, labeling, and packaging lines in a new greenfield facility.
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Computer Systems Validation Intern
Danaher
Fargo, North Dakota, United States
$0k–$0k
16d
Intern gaining hands-on experience in regulated industry operations alongside validation engineers and software developers.
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Senior Validation Engineer
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Katalyst Healthcares & Life Sciences
Columbus, OH, US
16d
Authoring, reviewing, and executing commissioning, qualification, and validation (CQV) documentation and test protocols for automated manufacturing or packaging equipment in a regulated environment.
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Engineer - Computer Systems Validation & IT Compliance
Bristolmyerssquibb
Devens - MA - US
$84k–$84k
16d
Execute Computer System Validation (CSV) and IT compliance activities for regulated IT systems in a fully automated manufacturing environment.
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QA Officer
Thermofisher
Brisbane, Australia
16d
QA Officer supporting Validation and Engineering teams to ensure regulatory compliance and quality standards in a GMP-regulated environment.
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Validation Analyst 3-1
Pciservices
Rockford, IL, USA
$0k–$0k
16d
Manage validation projects for large customer accounts, ensuring compliance with government and customer requirements for biopharma processes and systems.
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Ingenieur I Naturwissenschaftler I Techniker (m|w|d) für den Bereich Qualität und Validierung
Eurofins
Calw, BW, de
16d
Validating processes and assessing development results for cleaning, packaging, and sterilization in a sterile packaging environment.
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Manager, Process Performance Qualification
Pfizer
United States - Kansas - McPherson
$106k–$106k
17d
Leads a team of validation engineers for Process Qualification, Cleaning Validation, and Continued Process Verification (CPV) supporting sterile injectable manufacturing operations.
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Engineer II, Computer Systems Validation
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Thermo Fisher Scientific
Greenville, NC, US
17d
Support validation activities for automation systems, manufacturing equipment, and computerized systems to ensure compliance and operational readiness.
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Engineer II, Computer Systems Validation
Thermofisher
Greenville, North Carolina, USA
17d
Support validation activities for automation systems, manufacturing equipment, and computerized systems to ensure compliance and operational readiness.
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CQV Engineer
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Amaris Consulting
Singapore, S00, SG
17d
Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems in a GMP environment.
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Analytical Support Officer
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Gsk
Jurong, S00, SG
17d
Ensure analytical equipment and computer systems in quality laboratories are installed, validated, calibrated, and maintained according to quality standards and regulatory requirements.
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Computer Systems Validation Engineer
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Lupin
Somerset, NJ, US
$90k–$90k
17d
Ensure compliance with regulatory requirements (21 CFR Part 11, GAMP 5) for GMP laboratory and manufacturing systems, including networked, standalone, PLC, and SaaS systems.
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Validação de Sistemas
Qima
Goiânia, GO, br
17d
Ensures compliance of computerized systems and processes in regulated life sciences environments through validation lifecycle management.
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Senior Quality Engineering Specialist
Primemedicine
Cambridge
$111k–$111k
17d
Provides hands-on operational support for GxP software, equipment, calibration, preventive maintenance, and vendor oversight to ensure systems and equipment remain compliant and inspection-ready.
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Analytical Method Validation Specialist
Eurofins
Wavre, Wallonia, be
18d
Coordinate and author analytical method validation activities to ensure GMP compliance and maintain the validated state of methods within pharmaceutical QC operations.
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Validation Engineer
Sanofi
Le Trait
$42k–$42k
18d
Define and implement validation strategies for pharmaceutical manufacturing processes to ensure quality and regulatory compliance.
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Senior Quality Engineer, Software Validation
Edwards
USA - Utah – Salt Lake City
18d
Subject-matter expert and process owner for production and non-product software validation in a regulated manufacturing environment, ensuring software and documentation meet quality and regulatory requirements.
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Calibration Engineer (Temperature & Humidity) | Experienced as a Signatory for Lab
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Recruit Now Singapore Pte. Ltd.
Yishun, S00, SG
$5k–$5k
19d
Calibrate and validate temperature and humidity instruments and systems to ensure accuracy and regulatory compliance in controlled environments.
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Senior Quality Associate (Validation)
Pciservices
Moorabbin, AUS
22d
Lead the design, execution, and maintenance of a robust and compliant Validation Program for pharmaceutical manufacturing, covering Site Validation Master Plans, Cleaning VMP, and Qualification (IQ/OQ/PQ) of facilities, utilities, equipment, and software.
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Senior Validation Specialist
Csl
APAC, AU, Tullamarine, Seqirus
22d
Provide initial qualification, re-evaluation, and re-qualification support for equipment, computer systems, facilities, utilities, and processes in a biological/pharmaceutical manufacturing environment.
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Engineer III, Validation
Thermofisher
Plainville, Massachusetts, USA
$134k–$134k
22d
Perform validation activities including drafting, executing, reviewing, and approving quality documentation for clinical and commercial drug substance manufacturing of cell and gene therapy products.
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