Are you an expert in Liquid Chromatography that enjoys method development, troubling shooting and succeeding in a production chemistry environment? Join the Labcorp Biopharma Dose Analysis and put your knowledge and passion to work in early phases of drug development

 Research Associate Dose Analysis

Greenfield IN

The Research Associate in Dose Analysis will serve as the Lead Chemist working with HPLC/UPLC instruments analyzing samples and developing and validating methodologies for a variety of small and large molecule compounds in compliance with GLP regulations and SOPs. You will navigate systems, monitor and verify the quality of validation and production analytical runs, and perform troubleshooting In addition to being a technical subject matter expert for the Dose Analysis laboratory team, duties include and are not limited to:

• Sets up and performs method development and validation of various analytes in a variety of matrices with limited supervision

• Organizes, conducts and evaluates analytical results and testing.

• Participates in client visits as needed, assists in communicating technical information

• Documents work and maintains study documentation and laboratory records.

• Independently sets up, maintains, operates and performs routine and non-routine maintenance on general equipment, including problem identification and resolution.

• Informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect the integrity of the data and recommends corrective action.

• Suggests and performs modifications to test methods or procedures where precedence exists.

• Provides input and participates in project meetings, plans, monitors and guides project work.

• Performs QC review of data.

• Trains and assists less experienced staff.

• Writes, revises and reviews methods, SOPs and portions of reports and protocols.

• Effectively plans and utilizes personnel and resources for timely completion of assigned projects.

• Assists in evaluation of data for incorporation into written reports.

• Promotes a cohesive team environment.

Qualifications/Experience/Education

• BS/BA degree in science plus at least 4-5 years of previous laboratory experience.  Relevant experience may be substituted for education.

• Highly prefer 5+ years of HPLC and/or UPLC experience in laboratory. GC is a plus

• Requires 2+ years of troubleshooting of analytical equipment (HPLC/UPLC).

• Chromatographic Analytical method development is desired but not required.

• Familiar with the use of standard laboratory equipment.

• Effective communication (verbal and written), presentation and interpersonal skills.

What do we offer?

• Work with new compounds regularly to develop and validate methods for regulated analysis.

• Perform analysis to support studies in the early stages of drug development. 

• Great work culture where you?re part of a global organization making positive impacts in people?s lives 

• Great benefit offers that go into effect the 1st of the month. Unlimited time off, free lab testing, on-site gym, and much more

Benefits: 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. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable.  For more detailed information, please click here.