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Healthcare
› Computer System Validation
Computer System Validation
328 open positions
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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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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Validation Engineer
Soterahealth
Somercotes
22d
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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Senior Validation Engineer
Alcon
Fort Worth, Texas
22d
Execute validation and qualification activities for processes, equipment, systems, and facilities to ensure regulatory compliance and operational effectiveness.
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Engineer III, Validation
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Thermo Fisher Scientific
Plainville, MA, US
$134k–$134k
22d
Drafting, executing, and approving quality documentation for clinical and commercial drug substance manufacturing of cell and gene therapy products.
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Computer System Validation Specialist
New Zealand Clinical Research
Penrose, Auckland City
22d
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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Senior CQV Engineer-BioPharma
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Pharmeng Technology
Singapore, S00, SG
23d
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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Staff Quality Engineer, Microbiology and Sterilization
Stryker
Irvine, California
$96k–$96k
23d
Lead sterilization process development, validation, and requalification while ensuring microbiological control and biocompatibility compliance across the product lifecycle.
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ENGINEER
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Jackly Engineering Pte Ltd
Pasir Ris, S00, SG
23d
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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Lisen Builders Pte. Ltd.
Toa Payoh, S00, SG
23d
Develop, review, and maintain validation plans, protocols, and reports for computerized systems in pharmaceutical manufacturing to ensure regulatory compliance.
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Ingénieur/Spécialiste en Validation - Validation Engineer / Specialist 1
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Grifols
Montréal, QC, CA
23d
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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ENGINEER
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AG Builders
Toa Payoh, S00, SG
23d
Develop, review, and maintain validation plans, protocols, and reports for computerized systems in pharmaceutical manufacturing to ensure regulatory compliance.
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Validation Engineering Specialist I
Thermofisher
Whitby, Canada
$47k–$47k
24d
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
24d
Design, plan, and execute qualification/validations for high-complexity technical areas, services, equipment, and processes to ensure product quality.
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Validation Engineer I
Thermofisher
Groningen, Netherlands
24d
Planning, executing, and documenting validation activities for equipment, processes, and computer systems to ensure product quality and regulatory compliance.
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Senior Validation Engineer
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No Deviation Pte. Ltd.
Singapore, S00, SG
24d
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
25d
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
25d
Ensures compliance and performance of plant systems through equipment/system/process validation, requalification, and testing in a cGMP regulated environment.
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Technical Services Supervisor (Cikarang Site)
AstraZeneca
Indonesia - Cikarang
25d
Lead digital initiatives and support validation/qualification for IT systems in a pharmaceutical manufacturing environment.
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Senior Validation Engineer
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Promed Molded Products, Inc.
Plymouth, MN, US
25d
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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Validation Engineer
Freseniusglobal
Melrose Park, IL
$65k–$65k
25d
Execute equipment, system, and process validation studies (IQ/OQ/PQ) and requalifications in a cGMP regulated manufacturing environment to ensure compliance and performance.
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Process Validation Engineering Co-Op
Danaher
Fargo, North Dakota, United States
$0k–$0k
25d
Support process validation activities across the biologics manufacturing lifecycle, including process design, qualification, and continued verification.
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Pharmaceutical Project Executive
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Johnson Controls
Indianapolis, IN, US
$130k–$130k
25d
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 - CSV (OT)
Lonza
US - Vacaville, CA
$93k–$93k
25d
Leading and executing validation activities for manufacturing processes, equipment, computerized systems, and automation control systems to ensure compliance with regulatory requirements and internal quality standards.
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Equipment Validation Specialist
Thermofisher
Monza, Italy
25d
Ensuring compliance, quality, and operational excellence across facilities through comprehensive validation activities in pharmaceutical manufacturing, laboratory operations, and quality control.
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Gerente de Projetos - Manufatura
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As2 Group
São José dos Campos, SP, BR
$80k–$80k
25d
Manage development, validation, control, documentation, and implementation of manufacturing processes, equipment, and technology projects from conception to post-validation.
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SAP Compliance Manager m/f/d
↗
Cordenpharma
Lisboa, P11, PT
26d
Ensure compliance, validation, and audit readiness for SAP S/4HANA and connected applications in a highly regulated pharmaceutical environment.
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Manager of Manufacturing Applications - Onsite
Danaher
Remote
$95k–$95k
26d
Manage compliant, reliable, and validated enterprise manufacturing platforms supporting GxP-regulated operations in life sciences and diagnostics.
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Sr. Principal Quality Engineer
Cardinalhealth
TN-LaVergne Pack, US
$105k–$105k
26d
Develop and execute standardized cleaning validation protocols and master plans for a contract pharmaceutical packaging facility to ensure regulatory compliance.
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Computer Systems Validation Specialist III
Lonza
US - Portsmouth, NH
26d
Leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance, acting as the QA CSV representative for projects.
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Senior Validation Engineer
Lonza
NL - Geleen
$57k–$80k
26d
Lead and execute qualification and validation activities for equipment, facilities, utilities, and computerized systems in a biopharmaceutical production facility to ensure regulatory compliance and product quality.
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CSV/CQV Engineer – Kneat
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Jc Automation
Remote
26d
Develop, execute, and approve commissioning, qualification, and computer system validation (CSV/CQV) documentation for equipment, utilities, facilities, and automated systems in a regulated pharmaceutical manufacturing environment.
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MSAT Staff Scientist – Process Validation & Technology Transfer
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Thermo Fisher Scientific
Plainville, MA, US
$103k–$103k
26d
Own process validation strategy and lifecycle execution for biologics and viral vector programs, serving as technology transfer lead for incoming client and internal programs.
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Lab Validation
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Anter Consulting Pte. Ltd.
Singapore, S00, SG
26d
Qualify and validate environmental monitoring equipment (air samplers, particle counters) in GMP-regulated pharma/biotech settings.
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CQV Engineer
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Coalesce Management Consulting
Singapore, S00, SG
26d
Plan, execute, and document commissioning and qualification (CQV) for pharmaceutical process equipment and temperature-controlled units in a GMP environment.
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Senior Computer System Validation (CSV) Engineer
Cai
Melbourne, Victoria
29d
Lead validation activities for GxP-regulated systems in an advanced therapeutics facility, ensuring compliance with regulatory frameworks and supporting data integrity programs.
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QA Specialist
Cai
Melbourne, Victoria
29d
Support validation projects from initiation to completion, ensuring equipment, cleaning, analytical, and software processes meet regulatory standards and quality goals.
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Senior Pharmaceutical Commissioning Qualification Validation Engineer
Cai
Brisbane, Queensland
29d
Develop documentation, write and execute protocols, and generate summary reports for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
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Project Manager
Cai
Melbourne, Victoria
29d
Lead cGMP-commissioning, qualification, and validation (C&Q) projects for Life Sciences clients, ensuring operational readiness for process equipment and clean utilities.
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Packaging Engineer
LivaNova
Melbourne, Victoria
29d
Ensure medical device packaging activities comply with GMP, ISO 13485/11607, and regulatory standards through validation, testing, and documentation.
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CSV Engineer
Cai
Brisbane, Queensland
29d
Develop and execute Computer Systems Validation (CSV) protocols and test scripts for GxP and 21 CFR Part 11 compliant computerized systems in Life Sciences and Mission Critical industries.
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Sr. QA Computer System Validation Mgr.
4dmoleculartherapeutics
Hybrid
$126k–$126k
29d
Overseeing validation, compliance, and lifecycle management of GxP computer systems (clinical, quality, lab, enterprise, manufacturing) to ensure regulatory adherence and support business objectives.
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Computer Systems Engineer I
Catalent
Kansas City, MO
29d
Maintain computerized laboratory, manufacturing, and production systems while ensuring regulatory compliance and data integrity in a GMP environment.
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Validation Engineer
Abbott
Vietnam - Ho Chi Minh City
29d
Execute lifecycle qualification of manufacturing equipment, utilities, and facilities to ensure compliance with GMP and regulatory standards.
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Technical Process Engineer
Abbott
Ireland - Donegal Town
29d
Support Technical Services (STARS lab) engineering, validation, and maintenance activities for FreeStyle blood glucose test strips and sensors.
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Senior Validation Engineer
Cardinalhealth
IN-Indianapolis-Theranostics Commercial
$69k–$69k
29d
Lead planning, scheduling, and execution of validation projects (qualification, validation, requalification) for manufacturing processes, equipment, utility systems, products, cleaning, and sterilization in a cGMP environment.
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Quality Validation Engineer
Abbott
Ireland - Kilkenny
1mo
Creating and maintaining validation documentation for new and existing systems, processes, equipment, facilities, and software used in the manufacture, control, and storage of medical devices.
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Quality Engineer
Freseniusglobal
Melrose Park, IL
1mo
Develops and evaluates manufacturing quality and system standards, investigates validation issues, and verifies instrument maintenance.
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Transformation Project Qualification Lead- API
AbbVie
North Chicago, IL, us
1mo
Lead project teams to drive schedule, execution, risk management, and reporting for commissioning, qualification, and validation of new/modified equipment, facilities, utilities, and processes in line with project and quality objectives.
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Computerized Systems Validation (CSV) & Data Integrity Lead
Gehc
Cork
1mo
Lead Computerized Systems Validation (CSV) and Data Integrity programs to ensure GxP system compliance, inspection readiness, and alignment with regulatory requirements.
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