Assoc Scientist, Lab Operations

IQVIA Argentina; Indianapolis, Northern (IN, KY); Hybrid; USD 43,000 - 89,000; Full time

Job summary

IQVIA Laboratories in Indianapolis, Indiana, is seeking an Associate Scientist, Lab Operations to join our team. You will perform routine laboratory testing and document results to ensure data integrity per SOPs and regulatory requirements.

You will calibrate and maintain equipment, support quality investigations, and train staff while communicating clearly with cross-functional colleagues on assigned projects.

Qualifications

• Associate's degree or educational equivalent in medical technology is required
• 6 months of experience in a regulated laboratory environment
• Proficiency with buffers and solutions and routine lab calculations
• Certification required by country/state or regulatory body
• Experience with automation or specialized lab equipment

Responsibilities

• Perform and document analytical procedures per SOPs and regulatory guidelines
• Analyze data, confirm results within tolerances and flag unusual findings
• Prepare buffers and solutions and upload results into the LIMS
• Perform and document equipment calibration and maintenance
• Assist with quality investigations and procedural updates
• Train and guide laboratory personnel on routine procedures
• Communicate with cross-functional stakeholders on projects
• Support safety, quality, inventory, and 6S initiatives

Skills

Lab data analysis

Attention to detail

Regulated lab experience

Cross-functional communication

Education

Associate's degree in medical technology

Tools

LIMS

Laboratory automation equipment

Excel

Job description

We are seeking an Associate Scientist, Lab Operations to join IQVIA Laboratories in Indianapolis, Indiana.

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

Job Summary:

Perform routine laboratory testing and analysis to generate reliable data for drug development and clinical trials research. Document procedures and results in accordance with standard operating procedures and applicable regulatory requirements.

What You'll Be Doing:

• Perform and document analytical procedures in accordance with standard operating procedures and regulatory guidelines
• Analyze routine data, confirm results are within acceptable tolerances, and escape unusual findings or potential performance errors
• Prepare buffers and solutions and support the upload of analytical results into the laboratory information management system
• Perform and document assigned equipment calibration and maintenance activities
• Assist with quality investigations, deviations, procedural updates, and the implementation of laboratory process changes
• Train and guide laboratory personnel on routine procedures in areas of demonstrated competency
• Communicate clearly and promptly with cross-functional stakeholders and represent the laboratory team on assigned projects
• Support laboratory safety, quality, inventory, continuing education, and 6S initiatives
  

What We Are Looking For:

• An Associate's degree or educational equivalent in medical technology is required
• 6 months of experience in a regulated laboratory environment
• Proficiency with relevant laboratory techniques, including the preparation of buffers and solutions and the handling of batches and specimens
• Experience using automation or specialized laboratory equipment
• Proficiency with routine and some non-routine laboratory calculations, including averages, means, standard deviations, and quality control metrics
• An applicable certification required by country, state, or other relevant regulatory body is required
• Other equivalent combination of education, training, and experience may be accepted in lieu of degree
  

The Knowledge, Skills and Abilities Needed for This Role:

• Basic knowledge of the assigned technical area, laboratory systems, procedures, and applicable regulatory standards, such as Good Laboratory Practices
• Knowledge of laboratory safety, infection-control practices, standard precautions, and hazardous chemical handling
• Strong attention to detail and accuracy, with the ability to recognize unusual results and document work clearly
• Ability to manage multiple tasks and collaborate effectively with laboratory colleagues and cross-functional stakeholders
• Good computer skills, including proficiency with Microsoft Outlook, Word, and Excel
• Ability to support the onboarding and hands-on training of laboratory personnel
  

What We Offer You:

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

To learn more about our benefits, visit https://jobs.iqvia.com/benefits.

If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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.

The potential base pay range for this role, when annualized, is $42,700.00 - $89,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.