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LCMS Validation Scientist III

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Lab
Part Time, Per diem position
Listed on 2026-01-02
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 69000 - 81000 USD Yearly USD 69000.00 81000.00 YEAR
Job Description & How to Apply Below
Location: Indianapolis

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.

We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. We put our trust in science and in one another. This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner, as Labcorp Drug Development has helped pharmaceutical and biotech companies develop one-third of all prescription medicines on the market today.

We are seeking a LC/MS
Validation Scientist III to join our Bioanalytical team in Indianapolis, IN. As a Validation Scientist III, you will perform method validation, method update and stability testing using a variety of analytical techniques in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. In addition, you will provide downstream support of methods to associated groups and serve as a bioanalytical resource to the broader business.

Duties

and Responsibilities
  • Organize and perform routine to advanced level of method validation/testing (and all associated activities) with independence and efficiency in compliance with appropriate SOPs and regulatory agency guidelines.
  • Display advanced data interpretation and analytical instrumentation skills and respond to difficult procedural, technical, and quality questions with minimal guidance.
  • Assist in writing and review of reports, methods, protocols, and SOPs and maintain complete study documentation in compliance with regulatory guidelines (e.g. GLP and GCP) and department processes.
  • Inform Lead Scientist and/or management of any problems and/or deviations that may affect the integrity of the data and recommend corrective action.
  • Write and review training materials and deliver training/mentorship of staff in relevant techniques, procedures and provide expert advice on training requirements.
  • Support communications with external clients and other team members.
  • Participate in new equipment, instrument and methodology assessment and qualifications.
  • Demonstrate advanced time management skills and manage work on multiple assigned projects in a given week, and liaise and coordinate work activities with team members in order to deliver data.
  • Support others in their duties to ensure all scheduled operational activities are completed on each given day by effective and concise communication with team members, and ability to listen and discuss ideas in an open and professional manner.
  • Participate in process improvement initiatives.
Education/Experience
  • Bachelor’s Degree in Life Sciences, Pharmaceutical science or Chemistry with 3 years of relevant work experience or Master’s Degree with at least 1 year of relevant work experience in LC/MS method validation
  • Excellent communication and interpersonal skills
  • Proven ability to prioritize and manage time.
  • Excellent attention to detail
  • Able to utilize word processing, database, spreadsheet, and specialized software.
  • Work experience in GLP/GCP environment is a plus
Application Window

12/30/2025 thru 1/5/2026

Pay Range

$69k - $81k annually

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.

Benefits

Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including:
Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please .

Labcorp is proud to be an Equal Opportunity Employer

Labcorp strives for inclusion and belonging in the workforce and…

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