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Healthcare
› Computer System Validation
Computer System Validation
299 open positions
Computer System Validation Engineer (Senior)
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Integrix Solutions Pte. Ltd.
Singapore, S00, SG
15d
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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Validation Engineer
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Coalesce Management Consulting
Singapore, S00, SG
15d
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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Sr. Automation Engineering
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Juncos, PR, US
15d
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
15d
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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Staff Validation Engineer, Process and Cleaning
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Thermo Fisher Scientific
Greenville, NC, US
17d
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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Projektmanager Qualifizierung & Validierung Health (m/w/d)
Marktredwitz, BAYERN
18d
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
18d
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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Validation Lead Radiopharmacies
Gehc
Eindhoven
18d
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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Sr. Computer Systems Validation Analyst
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Katalyst Healthcares & Life Sciences
Foster City, CA, US
18d
Planning, leading, and executing Computer Systems Validation (CSV) for SCADA, PLC, and process control systems in GxP-regulated environments.
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ANALISTA DE VALIDAÇÃO DE SISTEMAS COMPUTADORIZADOS PLENO (GMP Quality Consulting)
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Jobbol
Osasco, SP, BR
18d
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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Computer Systems Validation Intern
Danaher
Fargo, North Dakota, United States
$0k–$0k
19d
Intern gaining hands-on experience in regulated industry operations alongside validation engineers and software developers.
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Validation Analyst 3-1
Pciservices
Rockford, IL, USA
$0k–$0k
19d
Manage validation projects for large customer accounts, ensuring compliance with government and customer requirements for biopharma processes and systems.
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Principal/Senior Principal Validation Engineer
Roche
Holly Springs
$95k–$95k
19d
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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Sr. Associate Validation Engineer
McKesson
USA, KY, Shepherdsville
$66k–$66k
19d
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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Engineer - Computer Systems Validation & IT Compliance
Bristolmyerssquibb
Devens - MA - US
$84k–$84k
19d
Execute Computer System Validation (CSV) and IT compliance activities for regulated IT systems in a fully automated manufacturing environment.
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Senior Validation Engineer
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Katalyst Healthcares & Life Sciences
Columbus, OH, US
19d
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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QA Officer
Thermofisher
Brisbane, Australia
19d
QA Officer supporting Validation and Engineering teams to ensure regulatory compliance and quality standards in a GMP-regulated environment.
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Ingenieur I Naturwissenschaftler I Techniker (m|w|d) für den Bereich Qualität und Validierung
Eurofins
Calw, BW, de
20d
Validating processes and assessing development results for cleaning, packaging, and sterilization in a sterile packaging environment.
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Engineer II, Computer Systems Validation
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Thermo Fisher Scientific
Greenville, NC, US
20d
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
20d
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
20d
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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Engineer II, Computer Systems Validation
Thermofisher
Greenville, North Carolina, USA
20d
Support validation activities for automation systems, manufacturing equipment, and computerized systems to ensure compliance and operational readiness.
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Computer Systems Validation Engineer
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Lupin
Somerset, NJ, US
$90k–$90k
20d
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
21d
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
21d
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
21d
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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Senior Quality Engineer, Software Validation
Edwards
USA - Utah – Salt Lake City
21d
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
22d
Calibrate and validate temperature and humidity instruments and systems to ensure accuracy and regulatory compliance in controlled environments.
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Senior Validation Specialist
Csl
APAC, AU, Tullamarine, Seqirus
25d
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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Senior Validation Engineer
Alcon
Fort Worth, Texas
25d
Execute validation and qualification activities for processes, equipment, systems, and facilities to ensure regulatory compliance and operational effectiveness.
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Validation Engineer
Soterahealth
Somercotes
25d
Technical representative for validation activities ensuring compliance with ISO standards, FDA regulations, and customer requirements in a highly regulated healthcare environment.
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Engineer III, Validation
Thermofisher
Plainville, Massachusetts, USA
$134k–$134k
25d
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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Senior Quality Associate (Validation)
Pciservices
Moorabbin, AUS
25d
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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Engineer III, Validation
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Thermo Fisher Scientific
Plainville, MA, US
$134k–$134k
25d
Drafting, executing, and approving quality documentation for clinical and commercial drug substance manufacturing of cell and gene therapy products.
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Specialist, QA Validation & Engineering
Catalent
Harmans, MD
$70k–$70k
25d
Provide Quality Assurance oversight for Facilities, Engineering, and Validation groups to ensure compliance with US regulations and industry standards for CGMP manufacturing of gene therapies and vaccines.
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Computer System Validation Specialist
New Zealand Clinical Research
Penrose, Auckland City
26d
Maintain the Computer System Validation (CSV) framework, policies, and templates to ensure digital systems comply with regulatory requirements and internal SOPs.
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ENGINEER
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Lisen Builders Pte. Ltd.
Toa Payoh, S00, SG
26d
Develop, review, and maintain validation plans, protocols, and reports for computerized systems in pharmaceutical manufacturing to ensure regulatory compliance.
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ENGINEER
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Jackly Engineering Pte Ltd
Pasir Ris, S00, SG
26d
Develop, review, and maintain validation plans, protocols, and reports for computerized systems in pharmaceutical manufacturing to ensure regulatory compliance.
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ENGINEER
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AG Builders
Toa Payoh, S00, SG
26d
Develop, review, and maintain validation plans, protocols, and reports for computerized systems in pharmaceutical manufacturing to ensure regulatory compliance.
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Staff Quality Engineer, Microbiology and Sterilization
Stryker
Irvine, California
$96k–$96k
26d
Lead sterilization process development, validation, and requalification while ensuring microbiological control and biocompatibility compliance across the product lifecycle.
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Senior CQV Engineer-BioPharma
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Pharmeng Technology
Singapore, S00, SG
26d
Draft, review, and execute Commissioning and Qualification (C&Q) documentation including plans, protocols, and reports for laboratory and production equipment in a GMP environment.
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Ingénieur/Spécialiste en Validation - Validation Engineer / Specialist 1
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Grifols
Montréal, QC, CA
26d
Lead the design, ownership, and execution of qualification and validation studies for utilities, facilities, equipment, automation, processes, and cleaning to ensure regulatory compliance.
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Validation Engineering Specialist I
Thermofisher
Whitby, Canada
$47k–$47k
27d
Support planning, execution, and documentation of validation activities for Process and Packaging Validation to ensure product quality and regulatory compliance.
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INGENIERO DE VALIDACION
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Pisa Farmacéutica
Guadalajara, JAL, MX
27d
Design, plan, and execute qualification/validations for high-complexity technical areas, services, equipment, and processes to ensure product quality.
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Senior Validation Engineer
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No Deviation Pte. Ltd.
Singapore, S00, SG
27d
Support commissioning, qualification, and validation (C&Q) activities for capital projects and routine maintenance in a GMP-regulated pharmaceutical environment.
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CSV & Equipment Compliance Manager
Lgc-Group
Petaluma, CA, us
$97k–$97k
28d
Ensure regulatory compliance for Computer System Validation (CSV) activities and deliver IT support for desktops and instrument workstations in GMP-regulated manufacturing environments.
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Validation Engineer
Freseniusglobal
Melrose Park, IL
$65k–$65k
28d
Ensures compliance and performance of plant systems through equipment/system/process validation, requalification, and testing in a cGMP regulated environment.
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Pharmaceutical Project Executive
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Johnson Controls
Indianapolis, IN, US
$130k–$130k
28d
Executive leadership for validated environment and laboratory construction programs (cleanrooms, BSCs, containment suites) across a campus, ensuring regulatory compliance and strategic governance.
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Senior Validation Engineer
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Promed Molded Products, Inc.
Plymouth, MN, US
28d
Ensure facility, equipment, utilities, and manufacturing processes consistently perform as intended to satisfy cGMP and regulatory expectations in a CDMO environment.
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Gerente de Projetos - Manufatura
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As2 Group
São José dos Campos, SP, BR
$80k–$80k
28d
Manage development, validation, control, documentation, and implementation of manufacturing processes, equipment, and technology projects from conception to post-validation.
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