LCMS Validation Scientist III

Labcorp • Indianapolis, IN

1d

About The Position

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.

Requirements

• 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

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.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level