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Associate Process Development Scientist Jobs in Olathe, KS

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Associate Process Development Scientist information

See Olathe, KS salary details

$18

$34

$55

How much do associate process development scientist jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for associate process development scientist in Olathe, KS is $34.73, according to ZipRecruiter salary data. Most workers in this role earn between $26.97 and $39.52 per hour, depending on experience, location, and employer.

What is the difference between Associate Process Development Scientist vs Process Development Scientist?

AspectAssociate Process Development ScientistProcess Development Scientist
Required CredentialsBachelor's or Master's in Life Sciences or Chemical EngineeringBachelor's or Master's, often with more experience or specialization
Work EnvironmentEntry-level, supporting process optimization in labs or manufacturingMore independent, leading process improvements and validations
Employer & Industry UsagePharmaceutical, biotech, or biotech manufacturing companiesSame industries, with increased responsibilities

The Associate Process Development Scientist typically supports process development tasks under supervision, focusing on experimental execution. In contrast, the Process Development Scientist takes on more independent roles, leading projects and process improvements. Both roles are common in biotech and pharmaceutical industries, with the main difference being experience level and scope of responsibilities.

What are popular job titles related to Associate Process Development Scientist jobs in Olathe, KS?

For Associate Process Development Scientist jobs in Olathe, KS, the most frequently searched job titles are:

Senior Principal Scientist (Sr. Research Scientist), Bioanalytical

410 ICR United States USA

Lenexa, KS • On-site

$92K - $117K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 28 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 (Sr. Research Scientist) at ICON in Lenexa, Kansas (KS). The Senior Principal Scientist (Sr. Research 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