LC-MS Method Validation Scientist

Labcorp

Madison (WI)

On-site

USD 33,000 - 50,000

Full time

9 hours ago
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Benefits offered by this job

Medical, Dental, Vision benefits
401(k) plan with company match
Paid Time Off (PTO) or Flexible Time

Job summary

Labcorp is seeking a Method Validation Scientist to support our Global Bioanalytical team in Madison, WI. The role focuses on routine to moderate method validation/testing in a GMP/GLP environment, with emphasis on data interpretation and coordination with internal clients.

The position requires a science degree and hands-on experience with regulated laboratory settings and LC-MS instrumentation, with onsite work in Madison, WI.

Qualifications

  • Bachelor’s degree in a science related field (e.g. chemistry biology, molecular biology, immunology, biochemistry etc.)
  • 1 year or more experience in advanced laboratory scientific methods or scientific investigation
  • 2 years or more of experience in a regulated laboratory setting
  • 1 year or more in a GLP or GMP environment
  • 1 year or more working with Liquid Chromatography–Mass Spectrometry environment

Responsibilities

  • Organize and perform routine to moderate level of method validation/testing with relative independence and efficiency in compliance with SOPs and regulatory guidelines.
  • Displays intermediate data interpretation and analytical instrumentation skills and works through problems with minimal assistance.
  • Reviews reports, methods, protocols, and SOPs and maintains complete study documentation in compliance with regulatory guidelines (e.g. GLP and GCP).
  • Informs Lead Scientist/management of problems and deviations that may affect data integrity; participates in corrective action of problems.
  • Manages work on assigned projects weekly and coordinates with team members to deliver data to internal clients.
  • Interacts with colleagues within Bioanalytical site.
  • 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.

Skills

Scientific data interpretation
Analytical instrumentation
Communication and teamwork

Education

Bachelor’s degree in science related field

Tools

Liquid Chromatography–Mass Spectrometry

Job description

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.

Labcorp is seeking a Method Validation Scientist to support our Global Bioanalytical team in Madison, WI.

Work Schedule

Monday – Friday, 8am - 4pm

  • This position is 100% onsite in Madison, WI.
Job 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.
  • 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.
  • 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.
Minimum Qualifications
  • Bachelor’s degree in a science related field (e.g. chemistry biology, molecular biology, immunology, biochemistry etc.)
  • 1 year or more experience in advanced laboratory scientific methods or scientific investigation
  • 2 years or more of experience in a regulated laboratory setting
  • 1 years or more in a GLP or GMP environment
  • 1 years or more working with Liquid Chroma LC-MStography and or Mass Spectrometer environment
Preferred Qualifications
  • 2 years or more Method Validation experience
  • 1 years or more Stability Testing
  • 1 years or more in a Bioanalytical Lab environment
  • 1 years or more in a Data Analysis environment and troubleshooting
Additional Job Standards
  • 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
Application Window Closes

9/22/26

  • Pay Range: $24.00 - $36.00 per hour

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

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.
  • Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.
  • Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO, For more detailed information, click here.
Labcorp Is Proud To Be An Equal Opportunity Employer

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

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