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In Lims Validation Jobs in Wisconsin (NOW HIRING)

LGC Group

Lab Services Technician II

Middleton, WI · On-site

$19.50 - $26/hr

Our tools play a key role in customer workflows from discovery applications through to commercial ... Log samples to LIMS and other IT infrastructure, update databases to ensure effective tracking of ...

LGC Group

Lab Services Technician II

Middleton, WI · On-site

$19.50 - $26/hr

Our tools play a key role in customer workflows from discovery applications through to commercial ... Log samples to LIMS and other IT infrastructure, update databases to ensure effective tracking of ...

LGC Group

Lab Services Technician II

Middleton, WI

$19.50 - $26/hr

Our tools play a key role in customer workflows from discovery applications through to commercial ... Log samples to LIMS and other IT infrastructure, update databases to ensure effective tracking of ...

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Supervisor Microbiology

Appleton, WI · On-site

Out of specification investigation, data trending, validation/verification testing. * Annual ... Lead role in current LIMS implementation and roll out to North America region. * Perform data ...

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All JobsIn Lims Validation JobsIn Lims Validation Jobs in Wisconsin

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.

What is an In Lims Validation specialist job description?

An In Lims Validation specialist is responsible for ensuring that laboratory information management systems (LIMS) are properly validated and compliant with industry standards. They develop validation protocols, execute testing, document results, and collaborate with quality assurance teams to maintain data integrity and system functionality. Proficiency in validation processes, regulatory requirements, and LIMS software is essential for this role.
What are popular job titles related to In Lims Validation jobs in Wisconsin? For In Lims Validation jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching In Lims Validation jobs in Wisconsin look for? The top searched job categories for In Lims Validation jobs in Wisconsin are:
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In Lims Validation jobs near you
Infographic showing various In Lims Validation job openings in Wisconsin as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Data Reviewer, Quality Control

Arrowhead Pharmaceuticals

Madison, WI • On-site

$80K - $90K/yr

Full-time

Re-posted 8 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

The Data Reviewer independently performs technical review of laboratory data and documentation to ensure compliance with analytical methods, specifications, GMP/GDP requirements, and data integrity standards. This role exercises independent judgment in evaluating data quality, identifying discrepancies, and resolving routine to moderately complex compliance issues. The Data Reviewer supports inspection readiness activities, contributes to continuous improvement initiatives, and serves as a technical resource to junior team members.

Responsibilities

  • Perform independent technical review of internal data and external laboratory data
  • Evaluate data for accuracy, completeness, and compliance with GMP and specifications
  • Independently evaluate, investigate, and document discrepancies, atypical results, and documentation inconsistencies to determine impact and ensure appropriate resolution
  • Review routine release and stability data, method validation data and report, IPC data, cleaning samples, and logbooks for traceability and compliance
  • Communicate and collaborate with laboratory staff and CDMOs to resolve data quality issues
  • Support audit readiness activities and participate in inspections
  • Maintain knowledge of laboratory systems and software for effective review
  • Recommend and support implementation of improvements to data review processes, documentation practices, and workflow efficiency
  • Provide guidance and onboarding support to junior reviewers on review practices, documentation standards, and GMP expectations
  • Embrace digital tools and opportunities for trend analysis, system suitability trending.
  • Perform additional duties as assigned in support of operations

Requirements

  • Bachelor's degree in chemistry or (any STEM degree) and 5+ years GMP experience, or a Master of Science (STEM degree) with minimum 3 years of experience in a cGMP laboratory (pharmaceutical CMO/CRO).
  • Experience with analytical data review and documentation practices
  • Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR, Appearance, pH, KF, UV spectrometry and microbiology testing.
  • Working knowledge of GMP/GDP and laboratory systems

Preferred

  • Working knowledge of USP, ISO, FDA and ICH guidelines
  • Familiarity with laboratory information systems, LIMS.
  • Strong verbal and written communication skills and ability to work with diverse professionals in a matrix environment.
  • Solid organizational skills with ability to adapt to changing priorities and deadlines.
Wisconsin pay range
$80,000—$90,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

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