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Lab Analyst III

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US, Lenexa KCIB (PRA)Posted Discovered via the company's careers siteMatch locked
Full time5+ years exp

About the role

Lab Analyst III-QC Analytical, Clinical Research (CRO) - Full-Time w/ benefits, Monday - Friday first shift schedule, 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.

III

to join a team of

bioanalytical professionals

supporting groundbreaking clinical research. As a

Lab Analyst III

you will be responsible for conducting

analytical QC testing

utilizing chromatography techniques like HPLC, as well as other techniques not limited to FTIR, Dissolution, Karl Fisher, Conductivity, Osmometer, liquid sampler, Disintegration, Visible Inspection, and Appearance. This role is essential in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations.

What You Will Be Doing

  • Performing laboratory tests and analyses in accordance with established protocols and procedures.
  • Routinely executing laboratory HPLC methods related to clinical studies.
  • Perform USP and EP test methods.
  • Participating in method development and validation, and qualification of compendial methods.
  • Assist in developing pharmaceutical formulations by testing various excipients, vehicles, etc.
  • 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

  • Bachelor's degree in biology, chemistry, or a related scientific field.
  • 5+ years of experience in a similar laboratory environment performing HPLC techniques. Clinical research of pharma environment strongly preferred.
  • Strong attention to detail and organizational skills, with the ability to follow protocols and maintain accurate records.
  • Basic proficiency in laboratory techniques and equipment operation, with a willingness to learn and develop new skills.
  • Good communication and teamwork abilities, with a proactive approach to supporting team objectives and deadlines.

#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

Not included in the source posting: about the role, qualifications.

Who can apply

The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.

Read automatically from the employer's posting text. Always confirm with the employer — requirements can change after a job is published.