Method Validation Scientist - II LC-MS

Labcorp•Madison, WI

1d•Onsite

About The Position

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. This role is for a Method Validation Scientist to support our Global Bioanalytical team in Madison, WI.

Requirements

Bachelor’s degree in a science related field (e.g. chemistry biology, molecular biology, immunology, biochemistry etc.)
3 years or more experience in advanced laboratory scientific methods or scientific investigation
3 years or more of experience in a regulated laboratory setting
2 years or more in a GLP or GMP environment
2 years or more working with Liquid Chroma LC-MStography and or Mass Spectrometer environment
Experience with of laboratory automation software, (analyst, e-workbook, Nautilus, Sciex, OS)
Experience in laboratory conduct and data interpretation
Experience and proficiency with laboratory analytical instrumentation
Excellent communication and interpersonal skills with excellent attention to detail

Nice To Haves

3 years or more Method Validation experience
2 years or more Stability Testing
3 years or more in a Bioanalytical Lab environment
2 years or more in a Data Analysis environment and troubleshooting

Responsibilities

Organize and perform routine to moderate level of method validation/testing (and all associated activities) with relative independence and efficiency in compliance with appropriate SOPs and regulatory agency guidelines.
Capable of executing advanced level of method validation activities with guidance.
Provide downstream support of methods to associated groups and serve as a bioanalytical resource to the broader business.
Displays intermediate data interpretation and analytical instrumentation skills and works through procedural and scientific routine problems and issues with minimal assistance.
Assists in review of reports, methods, protocols, and SOPs and maintains complete study documentation in compliance with regulatory guidelines (e.g. GLP and GCP) and department processes.
Informs Lead Scientist and/or management of any problems and/or deviations that may affect integrity of the data; participates in corrective action of problems.
Manages work on assigned projects in a given week, and liaise and coordinate work activities with team members in order to deliver data (right first time) to internal clients.
Effectively interacts with colleagues within Bioanalytical site.
Trains, and assists less experienced staff.
Participates in process improvement initiatives.
Supports communications with external clients and other team members.
Able to review work of others for overall accuracy, timeliness, completeness, and soundness of technical judgment.
Maintains a clean and safe laboratory work environment.
Performs other related duties as assigned.