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In Lims Validation Jobs in Missouri (NOW HIRING)

Jobgether

... in a remote environment. * Experience with cloud software, hardware, edge computing, IoT devices, and scientific instruments is strongly preferred. * Experience validating LIMS, MES, ELN, QMS, or ...

Scismic

Microbiology Manager

Springfield, MO

... in a high-volume, regulated testing environment. * Experience managing audits and implementing CAPA, method validations, and operational improvements. * Proficiency with LIMS and standard office ...

Scismic

Microbiology Manager

Springfield, MO · On-site

... in a high-volume, regulated testing environment. * Experience managing audits and implementing CAPA, method validations, and operational improvements. * Proficiency with LIMS and standard office ...

Scismic

Microbiology Manager

Springfield, MO · On-site

... in a high-volume, regulated testing environment. * Experience managing audits and implementing CAPA, method validations, and operational improvements. * Proficiency with LIMS and standard office ...

P&C Recruiting and HR

MO · On-site

Participate in continuous EHS improvement * Other duties as assigned EDUCATION & EXPERIENCE ... Valid driver's license required KNOWLEDGE, SKILLS & ABILITIES * Proficient with Microsoft Office

Eurofins

Bioassay Scientist

Columbia, MO · On-site

... in an agreed upon timeline. Train team upon completion of method establishment and validation ... Utilize laboratory information management system (LIMS) with proficiency. * Is able to utilize ...

Eurofins Scientific

Bioassay Scientist

Columbia, MO

... in an agreed upon timeline. Train team upon completion of method establishment and validation ... Utilize laboratory information management system (LIMS) with proficiency. * Is able to utilize ...

PATCO

Supervisor, QA/QC

Grandview, MO · On-site

... validation. Minimum Qualifications : Education : Bachelor's Degree (BS) in related field; A ... Maintain Lab Information Management System (LIMS) databases. * Communicates facility quality ...

PATCO

Supervisor, QA/QC

Grandview, MO · On-site

... validation. Minimum Qualifications : Education : Bachelor's Degree (BS) in related field; A ... Maintain Lab Information Management System (LIMS) databases. * Communicates facility quality ...

Albaugh LLC

Chemist

Saint Joseph, MO · On-site

... * Assist in method development, validation, and continuous improvement activities as needed ... Proficiency with computers and laboratory software (LIMS, Excel, data entry) * Excellent ...

Albaugh LLC

Chemist - 3rd Shift

Saint Joseph, MO · On-site

... * Assist in method development, validation, and continuous improvement activities as needed ... Proficiency with computers and laboratory software (LIMS, Excel, data entry) * Excellent ...

Altasciences

LCMS Scientist II

Columbia, MO · On-site

Lead the charge in developing and validating cutting-edge LC-MS/MS assays, harnessing your ... From advanced computer skills to familiarity with LIMS and electronic notebooks, you'll leverage ...

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All JobsIn Lims Validation JobsIn Lims Validation Jobs in Missouri

In Lims Validation information

What is the difference between In Lims Validation vs Laboratory Technician?

AspectIn Lims ValidationLaboratory Technician
CertificationsGMP, GLP, Validation certificationsTypically relevant certifications include Lab Technician or related training
Work EnvironmentQuality assurance, validation labs, regulated industriesLaboratories performing tests and experiments
Job FocusEnsuring LIMS systems meet regulatory standardsPerforming tests, recording data, maintaining lab equipment

In Lims Validation professionals focus on validating Laboratory Information Management Systems to ensure compliance with industry standards, while Laboratory Technicians perform routine testing and data collection. Both roles are essential in regulated labs but differ in scope and responsibilities.

How to validate a LIMS system?

Validating a LIMS (Laboratory Information Management System) involves developing a validation plan, performing installation and operational qualification, and documenting each phase to ensure the system meets user requirements and regulatory standards. It typically includes testing data integrity, system security, and functionality, often supported by validation protocols and traceability. Familiarity with regulatory guidelines such as 21 CFR Part 11 is essential for compliance.

What are popular job titles related to In Lims Validation jobs in Missouri?

For In Lims Validation jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching In Lims Validation jobs in Missouri look for?

The top searched job categories for In Lims Validation jobs in Missouri are:

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In Lims Validation jobs near you

CSV Validation Engineer

Jobgether

On-site

Contractor

Posted 5 days ago

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a CSV Validation Engineer based in Netherlands.

This is a senior, hands-on validation role supporting complex technology platforms used in pharmaceutical and other GxP-regulated environments.
You will lead risk-based computerized system validation across cloud applications, edge devices, scientific instruments, APIs, databases, and enterprise integrations.
Your work will help ensure regulated systems are fit for intended use, secure, reliable, and supported by complete, inspection-ready evidence.
You will collaborate closely with Engineering, Product, Quality, Operations, suppliers, and customers across the full system lifecycle.
The role combines regulatory expertise with technical investigation, requiring you to understand architectures, data flows, integrations, and system behavior.
You will also help mature validation practices by introducing practical structure, improving traceability, and leveraging modern engineering evidence.
This is an opportunity to make a direct impact in a growing environment where validation is treated as a critical engineering discipline rather than a documentation exercise.

Accountabilities
  • Develop and execute risk-based validation strategies for new systems, product features, integrations, infrastructure changes, releases, and customer implementations, defining appropriate scope according to intended use, system complexity, data-integrity risks, and regulatory requirements.
  • Create, maintain, and execute comprehensive CSV deliverables, including validation plans, requirements, functional and configuration specifications, risk assessments, test protocols, IQ/OQ/PQ documentation where applicable, traceability matrices, deviation records, and validation summary reports.
  • Translate regulatory and business requirements into clear, objective, testable acceptance criteria and ensure requirements, risks, tests, defects, and evidence remain fully traceable.
  • Validate complex technology ecosystems spanning browser applications, cloud services, APIs, databases, edge devices, scientific instruments, and integrations with LIMS, MES, ELN, QMS, and other regulated systems.
  • Assess and test data flows, transformations, mappings, unit conversions, synchronization, recovery behavior, and failure scenarios to ensure data is not lost, duplicated, corrupted, or incorrectly attributed.
  • Evaluate systems against FDA 21 CFR Part 11, EU GMP Annex 11, PIC/S GMP, GAMP 5, ALCOA+ data-integrity principles, and other applicable regulatory expectations.
  • Validate controls covering electronic records and signatures, audit trails, identity and access management, security, timestamps, retention, archival, backup, recovery, availability, and data migration.
  • Perform validation impact assessments for software releases, configuration changes, infrastructure updates, bug fixes, security events, deviations, CAPAs, and integration changes, determining appropriate regression and validation scope.
  • Maintain systems in a validated state by supporting periodic reviews, controlled retirement, migration, archival, decommissioning, and resolution of open validation discrepancies.
  • Partner with Engineering, Product, Quality, Operations, suppliers, and customer teams to review technical documentation and engineering evidence, avoid unnecessary testing duplication, and ensure GxP risks remain appropriately covered.
  • Prepare validation packages for Quality review, customer audits, supplier assessments, and regulatory inspections, clearly explaining validation strategies, risk decisions, controls, and test evidence.
  • Investigate unexpected results and discrepancies, distinguish meaningful product risks from low-value documentation issues, and support corrective and preventive actions.
  • Help establish consistent validation templates, processes, and practices within a growing organization while remaining practical, delivery-focused, and aligned with modern Computer Software Assurance principles.
Requirements
  • 10+ years of computerized system validation experience within pharmaceutical, biotechnology, life sciences, or another GxP-regulated environment, with proven ownership of end-to-end CSV activities.
  • Strong practical knowledge of FDA 21 CFR Part 11, EU GMP Annex 11, PIC/S GMP, GAMP 5, and ALCOA+ data-integrity principles.
  • Demonstrated experience applying risk-based validation and Computer Software Assurance approaches to complex systems.
  • Hands-on experience developing user requirements, risk assessments, validation plans, protocols, traceability matrices, deviations, summary reports, and IQ/OQ/PQ documentation where applicable.
  • Experience validating configurable software, SaaS applications, cloud platforms, laboratory systems, manufacturing systems, or integrated technology environments.
  • Strong understanding of electronic records, electronic signatures, audit trails, access controls, security, backup and recovery, retention, archival, and data migration.
  • Ability to understand and review technical documentation, system architectures, data flows, API specifications, engineering test evidence, and software change impacts.
  • Strong analytical and troubleshooting skills, with the ability to investigate discrepancies and understand how complex technical systems behave.
  • Excellent technical writing and documentation skills, with a focus on producing clear, defensible, objective, and inspection-ready evidence.
  • Ability to manage multiple validation workstreams independently, prioritize competing deliverables, and operate effectively with limited supervision.
  • Strong communication and collaboration skills, with the ability to work effectively across Engineering, Product, Quality, Operations, suppliers, and customer stakeholders in a remote environment.
  • Experience with cloud software, hardware, edge computing, IoT devices, and scientific instruments is strongly preferred.
  • Experience validating LIMS, MES, ELN, QMS, or similar enterprise integrations is an advantage.
  • Familiarity with REST APIs, relational databases, SQL, MQTT, asynchronous messaging, data transformations, field mappings, unit conversions, and multi-vendor data formats is beneficial.
  • Experience working within Agile software development environments and leveraging automated engineering tests as validation evidence is a plus.
  • Familiarity with cloud infrastructure qualification, supplier assessments, customer-specific deployments, deviation management, CAPA, change control, document control, and periodic review processes is desirable.
  • Exposure to Japanese PMDA expectations or other Asia-Pacific regulatory authorities, as well as customer audits or regulatory inspections, would be an advantage.
Benefits
  • Senior-level opportunity with significant ownership across computerized system validation and regulated technology platforms.
  • Hands-on exposure to complex cloud, edge, laboratory, manufacturing, API, and scientific-instrument environments.
  • Opportunity to influence and strengthen validation processes within a growing organization.
  • Collaboration with cross-functional technical, product, quality, and customer-facing teams.
  • Remote-friendly working environment with autonomy and responsibility.
  • Opportunity to apply modern risk-based validation and Computer Software Assurance practices.
  • Professional growth through exposure to evolving technologies, regulatory requirements, and complex GxP use cases.
  • The opportunity to contribute directly to the reliability, compliance, and audit readiness of mission-critical systems.
How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
 Why Apply Through Jobgether? 
 
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
 
 
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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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