The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
Senior Analytical Development Scientist
Madison, WI · On-site
$120 - $170/hr
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
Senior Analytical Development Scientist
Madison, WI · On-site
$120 - $170/hr
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
Senior Analytical Development Scientist
Madison, WI · On-site
$120 - $180/hr
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
New
Senior Analytical Development Scientist
Madison, WI · On-site
$120 - $180/hr
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC ...
New
Senior Scientist I, Analytical Development
Madison, WI · On-site
$115 - $135/hr
Independently design, develop, optimize, and validate analytical methods for drug substance/API and drug product development. * Develop specifications and test methods for raw materials, in-process ...
Senior Scientist I, Analytical Development
Madison, WI · On-site
$115 - $135/hr
Independently design, develop, optimize, and validate analytical methods for drug substance/API and drug product development. * Develop specifications and test methods for raw materials, in-process ...
Data Reviewer, Quality Control
Madison, WI · On-site
$95 - $125/hr
Review routine release and stability data, method validation data and report, IPC data, cleaning samples, and logbooks for traceability and compliance * Communicate/collaborate with laboratory staff ...
Data Reviewer, Quality Control
Madison, WI · On-site
$95 - $125/hr
Review routine release and stability data, method validation data and report, IPC data, cleaning samples, and logbooks for traceability and compliance * Communicate/collaborate with laboratory staff ...
Associate Scientist II, Quality Control
Madison, WI · On-site
$70 - $85/hr
Familiarity with analytical instrumentation, test method validation, data acquisition systems, and cGMP policies/practices. Preferred * Environmental Monitoring and/or cleanroom experience.
Associate Scientist II, Quality Control
Madison, WI · On-site
$70 - $85/hr
Familiarity with analytical instrumentation, test method validation, data acquisition systems, and cGMP policies/practices. Preferred * Environmental Monitoring and/or cleanroom experience.
Performance Validation Engineer
Fond Du Lac, WI · On-site
$73K - $106K/yr
The Performance Validation Engineer is responsible for developing, implementing, maintaining, and ... This role applies Lean Manufacturing principles, methodologies, and tools to drive operational ...
Performance Validation Engineer
Fond Du Lac, WI · On-site
$73K - $106K/yr
The Performance Validation Engineer is responsible for developing, implementing, maintaining, and ... This role applies Lean Manufacturing principles, methodologies, and tools to drive operational ...
Performance Validation Engineer
Fond Du Lac, WI · On-site
$73K - $106K/yr
The Performance Validation Engineer is responsible for developing, implementing, maintaining, and ... This role applies Lean Manufacturing principles, methodologies, and tools to drive operational ...
Performance Validation Engineer
Fond Du Lac, WI · On-site
$73K - $106K/yr
The Performance Validation Engineer is responsible for developing, implementing, maintaining, and ... This role applies Lean Manufacturing principles, methodologies, and tools to drive operational ...
Performance Validation Engineer
Fond Du Lac, WI · On-site
$73K - $106K/yr
The Performance Validation Engineer is responsible for developing, implementing, maintaining, and ... This role applies Lean Manufacturing principles, methodologies, and tools to drive operational ...
Performance Validation Engineer
Fond Du Lac, WI · On-site
$73K - $106K/yr
The Performance Validation Engineer is responsible for developing, implementing, maintaining, and ... This role applies Lean Manufacturing principles, methodologies, and tools to drive operational ...
Software Validation Engineer
Glendale, WI · On-site
Section Details Job Title Software Validation Engineer Job Type Contract Client Location Glendale ... Test Process and Methodologies. ISTQB Foundation Level is preferred. Good debugging ...
New
Quick apply
Software Validation Engineer
Glendale, WI · On-site
Section Details Job Title Software Validation Engineer Job Type Contract Client Location Glendale ... Test Process and Methodologies. ISTQB Foundation Level is preferred. Good debugging ...
New
HIL Validation Engineer
Glendale, WI · On-site
$110K - $120K/yr
... Validation, should have experience SWE4, SWE5 and SWE6, ASPICE • Experience in Automotive ... Process and Methodologies. ISTQB Foundation Level is preferred. • Good debugging ...
HIL Validation Engineer
Glendale, WI · On-site
$110K - $120K/yr
... Validation, should have experience SWE4, SWE5 and SWE6, ASPICE • Experience in Automotive ... Process and Methodologies. ISTQB Foundation Level is preferred. • Good debugging ...
HIL Validation Engineer
Glendale, WI · On-site
$110K - $120K/yr
... Validation, should have experience SWE4, SWE5 and SWE6, ASPICE • Experience in Automotive ... Process and Methodologies. ISTQB Foundation Level is preferred. • Good debugging ...
HIL Validation Engineer
Glendale, WI · On-site
$110K - $120K/yr
... Validation, should have experience SWE4, SWE5 and SWE6, ASPICE • Experience in Automotive ... Process and Methodologies. ISTQB Foundation Level is preferred. • Good debugging ...
BMS Validation Lead
Milwaukee, WI · On-site
... experince in HIL Validation Experience in Battery Management System (BMS) ECU development ... Good knowledge of Test Process and Methodologies. ISTQB Foundation Level is preferred. * Good ...
BMS Validation Lead
Milwaukee, WI · On-site
... experince in HIL Validation Experience in Battery Management System (BMS) ECU development ... Good knowledge of Test Process and Methodologies. ISTQB Foundation Level is preferred. * Good ...
Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer ... Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and ...
Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer ... Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and ...
BMS Validation Lead
Milwaukee, WI · On-site
... experince in HIL Validation Experience in Battery Management System (BMS) ECU development ... Good knowledge of Test Process and Methodologies. ISTQB Foundation Level is preferred. * Good ...
BMS Validation Lead
Milwaukee, WI · On-site
... experince in HIL Validation Experience in Battery Management System (BMS) ECU development ... Good knowledge of Test Process and Methodologies. ISTQB Foundation Level is preferred. * Good ...
Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer ... Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and ...
Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer ... Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and ...
Integration (Process Validation) Engineer
Trevor, WI · On-site
$70K - $85K/yr
Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer ... Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and ...
Quick apply
Integration (Process Validation) Engineer
Trevor, WI · On-site
$70K - $85K/yr
Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer ... Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and ...
Method Validation information
See Wisconsin salary details
$22.81 - $27.90
2% of jobs
$27.90 - $33
6% of jobs
$33 - $38.09
13% of jobs
$39.69 is the 25th percentile. Wages below this are outliers.
$38.09 - $43.19
13% of jobs
$43.19 - $48.28
11% of jobs
The median wage is $50.83 / hr.
$48.28 - $53.38
12% of jobs
$53.38 - $58.47
9% of jobs
$62.40 is the 75th percentile. Wages above this are outliers.
$58.47 - $63.57
13% of jobs
$63.57 - $68.67
13% of jobs
$68.67 - $73.76
6% of jobs
$73.76 - $78.86
3% of jobs
$22
$52
$78
How much do method validation jobs pay per hour?
What is a method validation?
A Method Validation job involves assessing and verifying analytical methods to ensure they produce reliable, accurate, and reproducible results. Professionals in this role typically work in pharmaceutical, biotechnology, or chemical industries, following regulatory guidelines such as ICH, USP, or FDA requirements. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and documenting results. Method validation ensures compliance with industry standards and guarantees product quality and safety.
What does a method validation do?
As a Method Validation professional, you will design, conduct, and document experiments to confirm that laboratory methods produce accurate and reproducible results under specified conditions. Typical daily tasks include preparing protocols, running validation samples, analyzing data, and preparing comprehensive validation reports for internal or regulatory review. You’ll work closely with scientists, quality assurance teams, and regulatory specialists to ensure compliance with industry standards. This collaborative environment provides opportunities to contribute to critical product development stages and to build expertise that supports career progression into quality management, regulatory affairs, or advanced analytical roles.
What are the key skills and qualifications needed for method validation?
To excel in Method Validation, a strong background in analytical chemistry, laboratory techniques, and scientific data analysis is typically required, often supported by a degree in chemistry, biochemistry, or a related field. Familiarity with validation protocols, industry regulations (such as GLP, GMP, or ISO standards), and analytical instrumentation (e.g., HPLC, GC, MS) is essential. Strong attention to detail, problem-solving skills, and effective collaboration and documentation abilities help professionals thrive in this position. These skills are vital to ensure that laboratory methods are reliable, regulatory-compliant, and suitable for their intended purposes.
What are the most commonly searched types of Method Validation jobs in Wisconsin?
The most popular types of Method Validation jobs in Wisconsin are:
What are popular job titles related to Method Validation jobs in Wisconsin?
For Method Validation jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Method Validation jobs in Wisconsin look for?
The top searched job categories for Method Validation jobs in Wisconsin are:

Fujifilm rating
8.5
Based on 70 frontline employees who took The Breakroom Quiz
33rd of 545 rated manufacturers
Job description
FCDI is seeking a Senior Analytical Development Scientist to support the company's continued growth and several ongoing projects within the Analytical Development (AD) team located in Madison, Wisconsin.
The AD team works cross-functionally to design, develop, optimize, qualify, and validate analytical methods used to characterize and release a diverse portfolio of induced pluripotent stem cell (iPSC)-derived cell therapy products for ocular, oncological, neurological, and other diseases.
We are seeking an experienced, self-motivated, and detail-oriented scientist who can serve as a technical authority within the analytical development team for method transfer and development in preparation for qualification and validation. In this hands-on laboratory role, you will collaborate closely with Analytical Development leadership, method validation and senior technical staff to ensure that methods are adequately prepared for technology transfer into QC. This will be achieved by collaborating with the organization's subject matter experts on analytical methods and validation strategies that are scientifically sound, phase-appropriate, compliant with regulatory expectations, and executed consistently.
The successful candidate will be motivated by the opportunity to plan, execute, and lead impactful work to help advance life-changing iPSC-derived therapies from development towards patient administration and enable FCDI to deliver these therapies efficiently, safely, and with the highest standards of quality. This is an onsite role located at our sites in the Madison, WI area.
Company OverviewAt FUJIFILM Cellular Dynamics, we're unlocking the power of human cells to change lives. Using revolutionary induced pluripotent stem cell (iPSC) technology, we drive advancements in drug discovery, disease modeling, cell therapy, research tools, and cell therapy manufacturing. Our mission is deeply meaningful, and we're looking for bold innovators to join us.
At FUJIFILM Cellular Dynamics, you'll thrive in a collaborative and cutting-edge environment that encourages creativity and celebrates breakthroughs. If you're ready to do work that makes a real impact and propels healthcare forward, this is your chance to be part of something extraordinary for science, patients, and yourself.
Our headquarters is in Madison, Wisconsin, a dynamic city celebrated for its lakes, parks, cultural richness, biotech leadership, and access to world-class academia.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers
Job DescriptionEssential Job Functions
- Independently conceive, plan, and lead analytical development activities for multiple internal and external programs, applying advanced scientific judgment to achieve project objectives and generate high-quality results.
- Develop, optimize, and transfer analytical methods across internal teams and external clients. Lead comparability studies to support method, process, or product changes. Partner closely with R&D and technical teams to support the deployment of new technologies and innovative development approaches
- Provide technical leadership and subject matter expertise for analytical method qualification and lifecycle strategies, including protocol development, establishment of acceptance criteria, execution, and definition of readiness criteria for qualification and formal method validation.
- Apply expert knowledge of relevant method guidance such as, but not limited to, ICH, USP, ISO and FDA to ensure analytical methods are scientifically sound, robust, fit for purpose, and compliant with regulatory expectations.
- Lead analytical gap assessments and risk evaluations to identify, prioritize, and proactively address technical and regulatory gaps in support of technology transfer, IND submission, project advancement, and product development objectives. Serve as a subject matter expert during technology transfer and analytical development activities.
- Analyze and interpret complex scientific data, troubleshoot technical challenges, and implement improvements to analytical methods, equipment, and work practices. Contribute scientific decision-making and enhance the team's technical capabilities.
- Prepare and maintain accurate, complete, and compliant documentation, including experimental records, protocols, technical reports, SOPs, method development and qualification documents, presentations, and other project-related records.
- Communicate scientific findings and project status to cross-functional teams, clients, and diverse internal or external audiences through technical presentations, written reports, and project summaries.
- Collaborate effectively with cross-functional teams to ensure analytical development activities meet project timelines, quality standards, and program requirements.
- Drive the execution of strategic initiatives that support business objectives and organizational growth within the AD function.
- Provide technical leadership, training, and mentorship to junior and mid-level scientists, promote consistency in experimental design, data analysis, and documentation, and lead small- to mid-sized project teams as assigned.
- Identify and develop innovative, potentially patentable components, methods, systems, or processes in support of the organization's research and development objectives.
- Perform other related duties as assigned.
Qualifications
- PhD in in a scientific or engineering discipline or other closely related field plus at least three (3) years of related experience; or a Master's degree in a comparable field plus at least seven (7) years of relevant experience; or a Bachelor's degree in a comparable field plus at least ten (10) years of related experience.
- Demonstrated experience leading method qualification and validation-readiness efforts, including protocol authorship, acceptance criteria definition, and application of ICH Q2 and Q14 principles to build risk-based analytical strategies in a relevant industry setting (preferably in a CDMO setting)
- Experience transitioning methods from development to QC protocol execution required.
- Demonstrated proficiency and independence with multiple molecular and/or cell-based analytical methods including flow cytometry, PCR, and ELISA; stem cell culture experience or experience with our differentiated cell product line is highly valuable.
- Demonstrated work ethic, initiative, the ability to multi-task, and intellectual curiosity to gain new technical skills.
- Proficiency in written and oral communication, with demonstrated ability to communicate effectively with internal and external stakeholders at all levels.
- Able to work well independently and in a team, with demonstrated experience training, guiding, and mentoring junior and mid-level staff.
- Strong problem-solving skills, with demonstrated ability to manage multiple technical projects independently, including flexibility to change project objectives quickly and willingly.
- Some evening and/or weekend work is required.
- Able to work at computer for extended periods of time.
- Able to work in laboratory hood for extended periods of time.
- Able to work with hazardous materials (i.e., chemicals, electrical equipment, and human tissue) without endangering oneself or others. Training will be required.
- Able to wear standard laboratory PPE.
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA InformationIf you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (fcdi-hr@fujifilm.com).
Employment Type: OTHERAbout Fujifilm
Sourced by ZipRecruiter
With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.
Industry
Chemical manufacturing
Company size
10,000+ Employees
Headquarters location
Minato-ku, Tokyo, JP