Lab Analyst II

ICON; Lenexa (KS); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Job summary

ICON is expanding its bioanalytical teams in the Greater Kansas City area. We seek a Lab Analyst II to join the QC analytical team, performing HPLC-based testing and data interpretation to support clinical studies and regulatory compliance.

The role requires a background in biology/chemistry, GMP/QC experience, and strong analytical skills, with opportunities for career growth in a values-driven environment.

Qualifications

• Bachelor’s degree in biology, chemistry, or related field.
• 3+ years of GMP and QC experience.
• Hands-on HPLC experience in a relevant environment.
• Strong technical skills with laboratory equipment and data analysis software.
• Commitment to high-quality standards and regulatory compliance.

Responsibilities

• Routinely execute laboratory HPLC methods for clinical studies following GMP/GDP.
• Perform routine tests including FTIR, Endotoxin, Dissolution, Karl Fischer, Conductivity, Osmometer, and more.
• Participate in method development, validation, and qualification of compendial methods.
• Assist in developing pharmaceutical formulations by testing excipients and vehicles.
• Inspect, release and manage production materials and samples to manufacturing facilities.

Skills

Effective communication

Teamwork

Education

Bachelor’s degree in biology, chemistry, or related field

Tools

HPLC

Job description

Lab Analyst II-QC Analytical, Clinical Research (CRO) - Full-Time w/ benefits, Lenexa, Kansas (KS)

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.

Looking to grow your career in support of real scientific advancements that bring new medicine to patients? Our bioanalytical teams in the Greater Kansas City area are growing! Join a culture that values you for your attitude, not just your experience.

What You Will Do:

We are currently seeking a Lab Analyst II to join our diverse and dynamic analytical QC team. As a Lab Analyst II you will be responsible for conducting analytical QC testing utilizing HPLC. You will analyze complex data sets, interpret results, and collaborate with senior analysts and peers to achieve project goals. Your role is crucial in maintaining the integrity of our laboratory’s data and ensuring compliance with regulatory standards.

Key Responsibilities Include:

• Routinely executing laboratory HPLC methods related to clinical studies, following GMP and GDP standards.
• Performing other routine laboratory tests and analyses including but not limited to, FTIR, Endotoxin, Dissolution, Karl Fisher, Conductivity, Osmometer, liquid sampler, Disintegration, Visible inspection, and Appearance.
• Participating in method development and validation, and qualification of compendial methods.
• Assist in developing pharmaceutical formulations by testing various excipients, vehicles, etc.
• Perform USP and EP test methods.
• Responsible for inspection, release and destruction of production materials, components, and chemicals to manufacturing facility; including intermediates.
• Responsible for sampling Raw Materials in an ISO Classified environment; including preparation and shipment of samples to the required laboratories.
• Operating and maintaining laboratory equipment, performing regular calibrations, and troubleshooting as needed.
• Supporting quality control activities by participating in the review and verification of test results and procedures.

Your Profile:

You will bring relevant scientific operations experience, along with the following qualifications and skills.

Required qualifications and experience:

• Effective communication and teamwork skills when executing logical problem solving and experimental strategy.

• Bachelor’s degree in biology, chemistry, or a related scientific field
• 3+ years of GMP and QC experience
• Hands on HPLC experience from a relevant environment
• Strong technical skills and proficiency in using laboratory equipment and software for data analysis and reporting.
• Commitment to maintaining high-quality standards and compliance.

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What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Please click here to apply