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Temporary Assay Development Scientist Jobs in Kansas

Senior Research Scientist

Lenexa, KS Ā· On-site

$92K - $117K/yr

In short, to be the partner of choice in drug development. That's our vision. We're driven by it ... Ligand binding assays * ELISA, ECLIA * PK, PD, and immunogenicity * Usage of relevant software (e.g.

You will support appropriate development, validation and use of analytical methods through sample ... Experience with ligand-binding assays. * Strong technical skills and proficiency in using ...

New

You will support appropriate development, validation and use of analytical methods through sample ... Experience with ligand-binding assays. * Strong technical skills and proficiency in using ...

New

You will support appropriate development, validation and use of analytical methods through sample ... Experience with ligand-binding assays. * Strong technical skills and proficiency in using ...

New

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

Showing results 21-40

Temporary Assay Development Scientist information

What is the difference between Temporary Assay Development Scientist vs Temporary Quality Control Analyst?

AspectTemporary Assay Development ScientistTemporary Quality Control Analyst
CredentialsBachelor's or Master's in Life Sciences, relevant lab experienceBachelor's in Life Sciences, laboratory experience in quality testing
Work EnvironmentResearch labs, product development teamsQuality control labs, manufacturing support
Industry UsageBiotech, pharmaceutical R&DManufacturing, pharmaceutical QC
Common Search IntentUnderstanding assay development rolesQuality testing and compliance roles

The Temporary Assay Development Scientist focuses on creating and optimizing laboratory assays for new products, often working in R&D settings. In contrast, the Temporary Quality Control Analyst primarily performs testing to ensure products meet quality standards during manufacturing. Both roles require laboratory experience but differ in their focus—development versus quality assurance—making them distinct yet related positions within the biotech and pharmaceutical industries.

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

To thrive as a Temporary Assay Development Scientist, you generally need a degree in biology, chemistry, or a related field, with experience in assay design, optimization, and validation. Familiarity with laboratory instrumentation, data analysis software, and experience with techniques such as ELISA, PCR, or cell-based assays is typically required. Strong problem-solving abilities, attention to detail, and effective collaboration and communication skills distinguish top performers in this role. These skills ensure reliable assay results, support project timelines, and contribute to the overall success of scientific research and product development.

What is a temporary assay development scientist?

Temporary Assay Development Scientists are professionals hired on a short-term basis to design, optimize, and validate laboratory assays, often for use in research, diagnostics, or pharmaceutical development. Their main role is to ensure that assays are reliable, reproducible, and meet the required standards for scientific or regulatory purposes. These scientists typically work in laboratory settings and may collaborate with other scientists or departments to support ongoing projects. Temporary positions may last from a few months to a year, depending on project needs and funding.

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

Temporary Assay Development Scientists often encounter challenges such as adapting quickly to new laboratory environments, meeting tight project deadlines, and mastering proprietary protocols unique to each organization. Since the role is temporary, there may be limited time to familiarize oneself with existing workflows and team dynamics. Proactively communicating with colleagues, being organized, and seeking clarification early on can help overcome these hurdles. Staying adaptable and open to feedback is key to succeeding in this fast-paced, collaborative setting.

Senior Principal Scientist, Bioanalytical

410 ICR United States USA

Lenexa, KS

Full-time

Posted 4 days ago


Job description

Senior Research Scientist- Onsite, Lenexa, KS- Full-Time; Flow Cytometry

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are excited to be seeking a new Senior Principal Scientist at ICON in Lenexa, Kansas (KS). The Senior Principal Scientist will lead and conduct scientific research aimed at advancing clinical trials and developing innovative therapies. You will manage sponsor programs, shape assay strategies, and provide expertise for new and complex modalities.

We are seeking candidates with proven method development and Spectral Flow Cytometry experience.

What You Will Do:

The Senior Principal Scientist is responsible for method development and validation for testing preclinical and clinical specimens using flow cytometry, and ligand-binding analytical methods. In addition, you will oversee transfer robust flow cytometry methods for further for bioanalytical testing.

Desired Experience (flow cytometry experience required, ligand binding experience preferred):

  • Flow cytometry

    • Experience with Spectral Flow

    • Panel design

    • Gating strategy design

    • Usage of cytometry software (e.g. FACSDiva, FCS express)

  • Ligand binding assays

    • ELISA, ECLIA

    • PK, PD, and immunogenicity

    • Usage of relevant software (e.g. SoftMax Pro, Watson)

Method Development

  • Designs and executes experiments for method development

  • Develops new scientific approaches to method development and communicates these to the global science team

  • Mentors junior scientists and advises operation on developed methods

  • Reviews and approves data of other scientists

  • Communicates with team members and management regarding project status, purpose, scheduling, problems, etc.

  • Lead communication with clients regarding project status.

Scientific

  • Maintain knowledge and skill in all techniques where you perform your work.

  • Provide scientific input to management and BD about new technology investments and lines of service.

  • Own discussions regarding scientific results with sponsors, together with project manager

  • Promotes ICON utilizing scientific skills through scientific communication such as external publication of posters and journal articles.

  • Perform R&D projects

  • Training of technicians on technical aspects

  • Mentor and train staff on scientific topics


Quality and Timely Work Execution

  • Takes initiative in process development and SOP/WI writing

  • Legible, logical and reproducible documentation of all experimentation

  • Has a thorough understanding and complies with GLP and other appropriate regulations

  • Develops rugged and economical assays

  • Performs data review of other scientist’s work

Sample Analysis and Assay Validation

  • Provides key assay input to the validation and bioanalysis team(s) to ensure successful execution

  • Assay troubleshooting

  • May perform and document maintenance, trouble-shooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel.

Qualifications 

  • Read, write and speak fluent English

  • Spectral flow cytometry experience

  • 10-15 years of relevant laboratory experience

  • MS or PhD with applicable research in a relevant scientific field, preferred

  • Presenter/Publisher in Regulated relevant field, preferred

#LI-KM3


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply