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Principal Scientist Assay Development Jobs in Wisconsin

Sr Biochemistry Scientist

Madison, WI · On-site

$100 - $125/hr

You are the Senior Biochemistry Scientist Illumina is looking for in joining our Test Method ... Advanced HPLC experience with proficiency in method development/optimization, and assay validation.

WI · On-site

$125 - $150/hr

... scientists and project leaders. You create an environment where people can learn, grow and excel. Whether that means discussing career development, assay troubleshooting or simply helping someone ...

... incoming assay and clinical data, developing bootstraps across different assay versions ... Familiarity with software development life cycle and best practices * Detail-oriented with strong ...

... incoming assay and clinical data, developing bootstraps across different assay versions ... Familiarity with software development life cycle and best practices * Detail-oriented with strong ...

WI · On-site

$100 - $125/hr

... assays, or analytical platforms. A Senior Scientist may operate either as a non-routine technical contributor for method development, transfer, or validation activities or as a key technical ...

WI · On-site

$100 - $125/hr

... assays, or analytical platforms. A Senior Scientist may operate either as a non‑routine technical contributor for method development, transfer, or validation activities or as a key technical ...

Our associates are involved in every stage of diagnostics, from ideation to development and ... Principal Clinical Scientist . This role is responsible for clinical trial strategies within the US ...

Research Scientist

Madison, WI · On-site

$78K - $156K/yr

The Research Scientist plays an active role in planning projects and experiments and is often the ... development of diagnostic assay products. Essential Duties Include, but are not limited to, the ...

Research Scientist

Madison, WI · On-site

$78K - $156K/yr

The Research Scientist plays an active role in planning projects and experiments and is often the ... development of diagnostic assay products. Essential Duties Include, but are not limited to, the ...

Showing results 21-40

Principal Scientist Assay Development information

What does a principal scientist assay development do?

A Principal Scientist in Assay Development leads the design, optimization, and validation of assays used for research, diagnostics, or drug development. They oversee laboratory teams, develop protocols, and ensure that assays meet regulatory and quality standards. Their role also involves troubleshooting complex scientific problems, collaborating with cross-functional teams, and staying current with technological advances in assay technologies. Principal Scientists play a key role in translating scientific concepts into reliable, reproducible assays that support broader organizational goals.

What are some common challenges faced by principal scientists assay development, and how can they be addressed?

Principal Scientists in Assay Development often encounter challenges such as optimizing assay sensitivity and specificity, troubleshooting inconsistent results, and scaling up assays for high-throughput screening. Addressing these issues requires strong analytical thinking, effective cross-functional collaboration with research, engineering, and quality assurance teams, and staying updated with the latest technological advances. Regularly reviewing validation protocols and actively participating in peer discussions can also help in overcoming technical hurdles and ensuring robust assay performance.

What are the key skills and qualifications needed to thrive as a principal scientist assay development, and why are they important?

To thrive as a Principal Scientist Assay Development, you need advanced expertise in biochemistry or molecular biology, a PhD or equivalent experience, and a strong background in assay design and validation. Familiarity with laboratory automation, data analysis software, and regulatory compliance systems such as GLP/GMP is typically required. Leadership, project management, and effective communication are crucial soft skills for guiding teams and collaborating across departments. These skills ensure robust assay performance, regulatory adherence, and efficient innovation in complex scientific environments.

What is the difference between Principal Scientist Assay Development vs Senior Scientist Assay Development?

AspectPrincipal Scientist Assay DevelopmentSenior Scientist Assay Development
CredentialsAdvanced degree (PhD or equivalent), extensive experienceMaster's or PhD, significant industry experience
Work EnvironmentLeads assay development projects, strategic planningExecutes assay development tasks, supports project teams
Employer & Industry UsagePharmaceutical, biotech, CROs, biotech companiesPharmaceutical, biotech, research labs

The main difference between Principal Scientist Assay Development and Senior Scientist Assay Development lies in their level of responsibility and leadership. Principal Scientists typically lead projects, set strategies, and have more extensive experience, while Senior Scientists focus on executing assays and supporting project goals. Both roles require strong technical expertise, but the Principal Scientist position involves higher-level decision-making and oversight.

What are popular job titles related to Principal Scientist Assay Development jobs in Wisconsin?

For Principal Scientist Assay Development jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Principal Scientist Assay Development jobs in Wisconsin look for?

The top searched job categories for Principal Scientist Assay Development jobs in Wisconsin are:

What cities in Wisconsin are hiring for Principal Scientist Assay Development jobs?

Cities in Wisconsin with the most Principal Scientist Assay Development job openings:

Infographic showing various Principal Scientist Assay Development job openings in Wisconsin as of July 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% In-person job distribution.

Sr Biochemistry Scientist

Socket.dev

Madison, WI • On-site

$100 - $125/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


Key responsibilities

  • Drive method development, optimization, characterization, and transfer of biochemical and enzymatic assays to support manufacturing operations.

  • Operate, maintain, and train others on laboratory equipment such as fragment analyzers, microplate readers, HPLCs, PCRs, and Tape Station units.

  • Prepare method transfer documentation, lead transfer activities, and ensure reproducibility and compliance with quality standards.


Job description

What if the work you did every day could impact the lives of people you know? Or all of humanity?At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.

You are the Senior Biochemistry Scientist Illumina is looking for in joining our Test Method Engineering team! In your future role at the Madison site of the global front-runnerin genetic sequencing, you will be one of a group of scientists who produce the fuel for Illumina’s sequencing, which is used in thestudyof genetic variation and function in realms from cancer research to agriculture.

As part of a diverse, self-directed team,you will be responsiblefor driving method development and validation activities in a cGMP laboratory for analysis of a broad range of enzymes using-state-of-art processes and equipment. You will also contribute to team driven improvement initiatives, engage in a curious and science-focused environment, and collaborate closely with cross-functional teams. We want your talent, genuine curiosity about applied science,enthusiasm for creative problem-solving, and drive to get things done.

Job duties include, but are not limited to:
  • Responsible for the development, optimization, characterization, and transfer of biochemical and enzymatic assays to support manufacturing operations.

  • Independently operate, maintain, and train others on key laboratory equipment platforms including fragment analyzers, microplate readers, HPLCs, PCRs, and Tape Station units.

  • Prepare method transfer documentation and lead method transfer activities to internal and external laboratories, ensuring reproducibility and compliance with quality standards.

  • Perform data processing, statistical evaluation, and interpretation of experimental results. Prepare technical reports, presentations, and documentation in accordance with internal GMP quality systems

  • Work closely with Quality Control, Manufacturing, Quality Assurance, Process Development, and global partner sites to support project execution.

  • Work independentlyand collaborativelyas part of a scientific team and participate in team meetings and initiatives.

  • Edit and revise area work instructions and standard operating procedures (SOPs)

  • Contribute to investigation and resolution of technical issues.

  • Assist with continuous improvement and sustaining activities.

  • Perform analyses of processes, identify gaps and deficiencies, and proactively propose practical, data driven solutions.

  • Maintain organization and inventory of lab supplies, equipment, and reagents.

  • Ability to lift 40 lbs. in weight and stand for periods of time during the manufacturing processes.

  • Other duties that may berequestedby management.

Requirements:
  • 6+ years of industry relevant laboratory experience in biotechnology, biomedical, biochemical or pharmaceutical industry.

  • Advanced HPLC experience with proficiency in method development/optimization, and assay validation.

  • Demonstrated ability to learn quickly and take initiative.

  • Demonstrated expertise in enzymatic assays and biochemical characterization techniques.

  • Excellent laboratory, organizational, and research skills.

  • Demonstrated ability to work on a diverse team.

  • Effective communicator with the ability to interface across functions.

  • Experienced in problem-solving and reasoning skills.

  • Proficient in Microsoft Word, PowerPoint & Excel.

Education:
  • Typically requires a degree in biochemistry, chemistry, biology, or related field. Bachelor’s degree with a minimum of6+ years of relevant industry experience or Master’s degree with a minimum of 4+ years of relevant industry experience or PhD with 2+years of relevant industry experience preferred.

The estimated base salary range for the Sr Biochemistry Scientist role based in the United States of America is: $91,100 - $136,700. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. The range reflects long‑term growth in the role; therefore, most candidates are hired between the minimum and middle of the range. Placement depends on experience, skills, location, and internal equity. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off.
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact accommodations@illumina.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.

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