ICON
Lab Analyst II
United States · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerICON
- LocationUnited States
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
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.
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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.
#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
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked