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Fortrea · 11 hours ago

LCMS Validation Scientist III

Indianapolis IN

Full-time

Onsite

Mid Level

$69K/yr - $81K/yr

3+ years exp

Labcorp is a leading global life sciences company that delivers answers for crucial health questions. They are seeking an LC/MS Validation Scientist III to perform method validation, method update, and stability testing while ensuring compliance with regulatory agency guidelines and standard operating procedures.

Clinical TrialsHealth Care

H1B Sponsor Likely

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 manages 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

Qualification

LC/MS method validationAnalytical instrumentationGLP/GCP environmentData interpretationSoftware proficiencyCommunication skillsTime managementAttention to detail

Required

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

Preferred

Work experience in GLP/GCP environment is a plus

Benefits

Medical

Dental

Vision

Life

STD/LTD

401(k)

Paid Time Off (PTO) or Flexible Time Off (FTO)

Tuition Reimbursement

Employee Stock Purchase Plan

Company

Fortrea

Fortrea is a provider of comprehensive Phase I through IV clinical trial management, clinical pharmacology, patient access solutions.

Founded in 2023

Durham, North Carolina, USA

10001+ employees

https://www.fortrea.com

H1B Sponsorship

Fortrea has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Trends of Total Sponsorships

2025 (12)

2024 (25)

2023 (6)