Associate Scientist - #191965
IQVIA
Date: 3 weeks ago
City: Livingston
Contract type: Full time
IQVIA Laboratories
IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialize in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies.
Join us on our exciting journey!
Job Overview
Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines.
Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.
Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.
Assists in quality investigations, deviations, and resolution.
Performs and document calibration and maintenance of laboratory equipment as assigned.
Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.
Assists in the review and update of laboratory procedures and techniques.
Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.
Requirements
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialize in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies.
Join us on our exciting journey!
Job Overview
Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines.
Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.
Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.
Assists in quality investigations, deviations, and resolution.
Performs and document calibration and maintenance of laboratory equipment as assigned.
Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.
Assists in the review and update of laboratory procedures and techniques.
Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.
Requirements
- Bachelor's Degree or equivalent combination of education and experience required, with a focus on chemistry, biology, or medical laboratory technology in some CAP/CLIA lab locations.
- Minimum 6 months of experience in a regulated laboratory environment.
- Proficiency in laboratory techniques, regulatory standards such as GLP, laboratory safety, and infection control practices.
- Proficiency in relevant laboratory techniques and experience with automation or specialized laboratory equipment.
- Ability to perform routine and non-routine laboratory calculations accurately, strong computer skills, capability to handle multiple tasks simultaneously, attention to detail, and effective collaboration with internal stakeholders are essential for the role.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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