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Lab Analyst II

ICON plcICON plc·Pharmaceutical Services

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6 days

Sponsorship

H-1B history

This company has a track record of sponsoring H-1B visas.

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About the role

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.

#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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Aplyr's read

ICON plc is a leading global provider of outsourced services in the pharmaceutical industry, attracting professionals in clinical research and data management.

Synthesized from recent postings & public sources

What's promising

  • •ICON plc has a strong global presence, enhancing its ability to manage international clinical trials effectively.
  • •The company offers diverse career opportunities across various roles in clinical research and data analysis.
  • •ICON's focus on innovation in pharmaceutical services supports its competitive edge in the industry.

What to watch

  • •The pharmaceutical industry is highly regulated, which may limit flexibility in project execution.
  • •ICON's reliance on large pharmaceutical clients could pose risks if partnerships dissolve.
  • •The competitive nature of the CRO market may pressure ICON to maintain cost efficiency.

Why ICON plc

  • •ICON plc specializes in comprehensive outsourcing solutions, differentiating it from competitors with narrower service scopes.
  • •The company's integration of technology in clinical trials offers a unique advantage in data management.
  • •ICON's strategic acquisitions have expanded its capabilities and market reach significantly.

Aplyr’s read is generated by AI from public sources. Was it useful?

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About ICON plc

ICON plc is a global provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology, and medical device industries.

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