Quality Control Laboratory Analyst 3

ICON Strategic Solutions; Lenexa (KS); On-site; USD 70,000 - 95,000; Full time

Job summary

ICON Strategic Solutions in Lenexa, KS is seeking a Lab Analyst III to join a bioanalytical team supporting clinical research. The role centers on analytical QC testing using chromatography (HPLC) and related techniques such as FTIR, dissolution, and Karl Fischer.

You will ensure accurate data, follow SOPs, and contribute to method validation and development, material sampling in ISO environments, and testing of production materials. Strong attention to detail and teamwork are essential.

Qualifications

• Bachelor's degree in biology or chemistry required.
• 5+ years of experience in a lab performing HPLC techniques.
• GMP and GDP experience preferred.
• Experience with method validation or method development is a plus.

Responsibilities

• Perform laboratory tests and analyses per established protocols.
• Routinely execute HPLC methods related to clinical studies.
• Perform USP and EP test methods.
• Assist in method validation, development, and qualification of compendial methods.
• Sample Raw Materials in ISO classified environments and ship samples as needed.
• Inspect, release, and destruction of production materials and chemicals to manufacturing.
• Operate and maintain laboratory equipment and perform calibrations.
• Support QC activities by reviewing test results and procedures.

Skills

Analytical QC

Team collaboration

Detail oriented

Good communication

Education

Bachelor's degree in biology or chemistry

Tools

HPLC

FTIR

Karl Fischer

Dissolution

Job description

QC Lab Analyst III - Onsite in Lenexa, KS

We're currently seeking a Lab Analyst 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.
• GMP and GDP experience
• Experience with method validation or method development (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.