A key focus will be coordinating activities in technical projects, develop and validate analytical methods and concepts to ensure quality and performance of our highplex products. You will also ...
A key focus will be coordinating activities in technical projects, develop and validate analytical methods and concepts to ensure quality and performance of our highplex products. You will also ...
Biochemistry, Biology, Proteomics or related discipline Technical Expertise • Experience in analytical method development (validation experience is a plus) • Hands on experience in molecular ...
Biochemistry, Biology, Proteomics or related discipline Technical Expertise • Experience in analytical method development (validation experience is a plus) • Hands on experience in molecular ...
Experience troubleshooting analytical instrumentation * Experience performing bioanalytical procedures and cell-based assays * Experience with method validation and transfer
Experience troubleshooting analytical instrumentation * Experience performing bioanalytical procedures and cell-based assays * Experience with method validation and transfer
This role supports Eagle Analytical's Quality Management System by reviewing analytical methods, validation documentation, laboratory data, reports, and quality investigations while ensuring ...
This role supports Eagle Analytical's Quality Management System by reviewing analytical methods, validation documentation, laboratory data, reports, and quality investigations while ensuring ...
Quality Control Chemist
Houston, TX · On-site
This role supports Eagle Analytical's Quality Management System by reviewing analytical methods, validation documentation, laboratory data, reports, and quality investigations while ensuring ...
Quality Control Chemist
Houston, TX · On-site
This role supports Eagle Analytical's Quality Management System by reviewing analytical methods, validation documentation, laboratory data, reports, and quality investigations while ensuring ...
Analytical Chemist - Metals
Conroe, TX · On-site
... methods, SOPs, and regulatory protocols * Operate, calibrate, troubleshoot, and maintain ICP and ICP-MS instrumentation * Review, interpret, validate, and document analytical data within LIMS
Analytical Chemist - Metals
Conroe, TX · On-site
... methods, SOPs, and regulatory protocols * Operate, calibrate, troubleshoot, and maintain ICP and ICP-MS instrumentation * Review, interpret, validate, and document analytical data within LIMS
Develop, optimize, and validate analytical methods (HPLC, LC-MS, GC-MS, ICP-MS, UV-Vis, etc.) to support R&D, manufacturing, and quality control needs. * Analyze raw materials, intermediates, and ...
Develop, optimize, and validate analytical methods (HPLC, LC-MS, GC-MS, ICP-MS, UV-Vis, etc.) to support R&D, manufacturing, and quality control needs. * Analyze raw materials, intermediates, and ...
... EPA methods, laboratory procedures, and quality standards * Prepare, process, and analyze ... Review, validate, and document analytical results within the Laboratory Information Management ...
... EPA methods, laboratory procedures, and quality standards * Prepare, process, and analyze ... Review, validate, and document analytical results within the Laboratory Information Management ...
... EPA methods, laboratory procedures, and quality standards * Prepare, process, and analyze ... Review, validate, and document analytical results within the Laboratory Information Management ...
... EPA methods, laboratory procedures, and quality standards * Prepare, process, and analyze ... Review, validate, and document analytical results within the Laboratory Information Management ...
Sr Staff Scientist - Medical Devices
Stafford, TX · On-site
$128K - $184K/yr
Lead the design and execution of product evaluations, analytical methods, and validation studies for IVF Media solutions. * Provide biological risk assessments and technical support to manufacturing ...
Sr Staff Scientist - Medical Devices
Stafford, TX · On-site
$128K - $184K/yr
Lead the design and execution of product evaluations, analytical methods, and validation studies for IVF Media solutions. * Provide biological risk assessments and technical support to manufacturing ...
Quality Control Specialist
El Paso, TX · On-site
Support method validation, data analysis, and troubleshooting of experiments. Ensure compliance with safety rules, company policies, and regulatory standards. Maintain laboratory housekeeping ...
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Quality Control Specialist
El Paso, TX · On-site
Support method validation, data analysis, and troubleshooting of experiments. Ensure compliance with safety rules, company policies, and regulatory standards. Maintain laboratory housekeeping ...
Chemist
Austin, TX · On-site
$71K - $119K/yr
Experience troubleshooting analytical instrumentation * Experience performing bioanalytical procedures and cell-based assays * Experience with method validation and transfer Expected Compensation:
Chemist
Austin, TX · On-site
$71K - $119K/yr
Experience troubleshooting analytical instrumentation * Experience performing bioanalytical procedures and cell-based assays * Experience with method validation and transfer Expected Compensation:
Validate and troubleshoot analytical methods * Developing test plans, quotes and documenting test process and preparing reports summarizing findings to customers * Overall project management and ...
Validate and troubleshoot analytical methods * Developing test plans, quotes and documenting test process and preparing reports summarizing findings to customers * Overall project management and ...
Define validation metrics, pass/fail criteria and reporting methodologies to ensure repeatable and high-quality analysis * Guide development of custom workload generators and micro-benchmarks where ...
Define validation metrics, pass/fail criteria and reporting methodologies to ensure repeatable and high-quality analysis * Guide development of custom workload generators and micro-benchmarks where ...
Validate and troubleshoot analytical methods * Developing test plans, quotes and documenting test process and preparing reports summarizing findings to customers * Overall project management and ...
Validate and troubleshoot analytical methods * Developing test plans, quotes and documenting test process and preparing reports summarizing findings to customers * Overall project management and ...
Validate and troubleshoot analytical methods * Developing test plans, quotes and documenting test process and preparing reports summarizing findings to customers * Overall project management and ...
Validate and troubleshoot analytical methods * Developing test plans, quotes and documenting test process and preparing reports summarizing findings to customers * Overall project management and ...
Define validation metrics, pass/fail criteria and reporting methodologies to ensure repeatable and high-quality analysis * Guide development of custom workload generators and micro-benchmarks where ...
Define validation metrics, pass/fail criteria and reporting methodologies to ensure repeatable and high-quality analysis * Guide development of custom workload generators and micro-benchmarks where ...
Quality Scientist
Plano, TX · On-site
Lead and support analytical method qualification, validation, and transfer activities, including protocol review, data evaluation, receiving site alignment, and adherence to ICH Q2/Q14, FDA, and EMA ...
Quality Scientist
Plano, TX · On-site
Lead and support analytical method qualification, validation, and transfer activities, including protocol review, data evaluation, receiving site alignment, and adherence to ICH Q2/Q14, FDA, and EMA ...
Strong knowledge of analytical chemistry principles. * Hands-on experience with USP, ISO, and ASTM testing methodologies. * Understanding of chemical method validation and verification. * Ability to ...
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Strong knowledge of analytical chemistry principles. * Hands-on experience with USP, ISO, and ASTM testing methodologies. * Understanding of chemical method validation and verification. * Ability to ...
Define validation metrics, pass/fail criteria and reporting methodologies to ensure repeatable and high-quality analysis * Guide development of custom workload generators and micro-benchmarks where ...
Define validation metrics, pass/fail criteria and reporting methodologies to ensure repeatable and high-quality analysis * Guide development of custom workload generators and micro-benchmarks where ...
Analytical Method Validation information
See Texas salary details
$21.05 - $25.76
2% of jobs
$25.76 - $30.46
6% of jobs
$30.46 - $35.16
13% of jobs
$36.63 is the 25th percentile. Wages below this are outliers.
$35.16 - $39.86
13% of jobs
$39.86 - $44.57
11% of jobs
The median wage is $46.92 / hr.
$44.57 - $49.27
12% of jobs
$49.27 - $53.97
9% of jobs
$57.60 is the 75th percentile. Wages above this are outliers.
$53.97 - $58.68
13% of jobs
$58.68 - $63.38
13% of jobs
$63.38 - $68.08
6% of jobs
$68.08 - $72.79
3% of jobs
$21
$48
$72
How much do analytical method validation jobs pay per hour?
What are the key skills and qualifications needed to thrive in the Analytical Method Validation position, and why are they important?
To thrive in Analytical Method Validation, you need a strong background in analytical chemistry or related sciences, precision in laboratory work, and experience with method development and validation protocols, often supported by a relevant degree. Familiarity with instrumentation such as HPLC, GC, and mass spectrometry, as well as knowledge of regulatory standards like ICH, FDA, or USP, and proficiency in laboratory information management systems (LIMS) are key. Attention to detail, critical thinking, and effective communication are important soft skills for troubleshooting and collaborating with cross-functional teams. These skills ensure robust, compliant analytical methods that underpin product quality and regulatory approval.
What is an Analytical Method Validation job?
An Analytical Method Validation job involves developing, assessing, and documenting laboratory methods to ensure they produce reliable and accurate results. Professionals in this role validate methods according to regulatory guidelines (such as ICH, USP, or FDA) by evaluating parameters like accuracy, precision, specificity, and robustness. They work in industries like pharmaceuticals, biotechnology, and chemicals to ensure compliance with quality standards. The role also requires troubleshooting analytical issues and maintaining validation records to support regulatory audits.
What does a typical day look like for someone working in Analytical Method Validation?
A typical day in Analytical Method Validation involves developing and executing protocols to verify that laboratory methods are reliable, accurate, and consistent with industry regulations. You'll spend time in the lab conducting experiments, analyzing sample data, documenting results, and preparing detailed validation reports for regulatory submission. Collaborating with quality assurance, regulatory teams, and other scientists is common to address findings and ensure alignment with project goals. This role combines hands-on technical work with critical data review and cross-disciplinary teamwork, offering a dynamic and intellectually engaging work environment.

Full-time
Posted 16 days ago
Thermo Fisher Scientific rating
7.7
Based on 415 frontline employees who took The Breakroom Quiz
196th of 528 rated manufacturers
Job description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information:
Olink, part of Thermo Fisher Scientific, is dedicated to advancing the understanding of human disease through proteomics. Olink panels provide innovative, high-quality solutions for human protein biomarker discovery, enabling researchers to measure thousands of proteins simultaneously from just a few microliters of blood. Using highly specific and thoroughly validated assays with a wide dynamic range, Olink’s technology overcomes traditional limitations in protein analysis and supports deeper insights into human biology and disease.
Job description
We are seeking an experienced and driven Staff Development Engineer or Scientist to join our innovative R&D organization and the Analytical Development team. The team currently consists of 12 dedicated team members. The role is based in our Uppsala office, reporting to Manager, Analytical Development.
In this role, you will play a central part in developing, optimizing, and implementing analytical quality control (QC) methods for reagents and kit products. You will contribute to advancing our proteomics platform while ensuring robust, reliable, and scalable analytical solutions.
A Day in the Life
You will collaborate across functions and contribute to cutting-edge projects within proteomics. A key focus will be coordinating activities in technical projects, develop and validate analytical methods and concepts to ensure quality and performance of our highplex products. You will also perform advanced data analysis and present conclusions to guide technical decisions.
Key Responsibilities
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Design and execute experiments to develop and optimize analytical QC methods
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Perform complex data analysis and identify key parameters influencing performance
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Lead activities in technical project, mentor colleagues and contribute to building team expertise
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Troubleshoot technical challenges and deliver practical, high-quality solutions
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Collaborate with cross-functional teams in R&D, production, and quality
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Drive continuous improvement initiatives to enhance robustness, efficiency, and scalability of analytical methods
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Maintain high-quality documentation in line with scientific and regulatory standards
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Stay current with scientific advancements and integrate best practices into development workflows
Education & background
• PhD in life science with relevant industry experience, or
• MSc in Engineering /Life Science (or equivalent) with significant industrial experience.
Preferred Areas of Study: Biochemistry, Molecular Biology, Proteomics or related discipline
Technical Expertise
• Strong experience in analytical method development , verification, and validation methodologies
• Hands on experience in molecular biology and protein analysis techniques, such as:
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protein affinity assays
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PEA, PCR, NGS
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extensive experience working with liquid handling robots
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automated workflows and analytical instrumentation
Skills & competencies
• Excellent analytical thinking and problem-solving capabilities
• Proven ability to design experiments and interpret complex datasets
• Experience leading activities in technical projects and collaborating with diverse teams
• Strong documentation skills and attention to detail
• Effective communication skills, preferably in both Swedish and English
• Ability to work independently while collaborating effectively in cross-functional teams
• Adaptability and proactive mindset in a dynamic environment
• Project management capabilities and ability to manage multiple priorities
Additional merits
• Track record of scientific contributions (publications, presentations, patents)
• Proficiency in statistical analysis and DOE methodology
• Experience developing or applying high‑throughput analytical techniques and automated workflows
Why Join Us?
At Olink, Thermo Fisher Scientific, you will be part of a nurturing team that values integrity, innovation, and involvement. We offer an encouraging environment where your diverse experiences and perspectives are appreciated, enabling you to thrive and excel in your career.
Please note that no screening or interviews will occur until the beginning of August due to the summer holiday season. The last for applications is on the 4th of August.
What Thermo Fisher Scientific employees say
Pay
Benefits
Hours and flexibility
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About Thermo Fisher Scientific
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
10,000+ Employees
Headquarters location
Waltham, MA, US
Year founded
1956