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Senior Manager, LC-MS Bioanalysis

Job in Madison, Dane County, Wisconsin, 53703, USA
Listing for: Labcorp
Full Time position
Listed on 2026-08-05
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 130000 - 160000 USD Yearly USD 130000.00 160000.00 YEAR
Job Description & How to Apply Below

Senior Manager, LC-MS Bioanalysis

Location:

Madison, WI, On-Site

Work Schedule:

Monday thru Friday

Lead the Future of Bioanalytical Science

Are you a proven leader in LC-MS bioanalysis with a passion for developing high-performing teams, advancing scientific excellence, and driving operational success? We are seeking a Senior Manager, LC-MS Bioanalysis to lead our Method Development and Validation functions, providing strategic and operational leadership within a fast-paced, regulated bioanalytical environment.

In this role, you will oversee teams responsible for developing, validating, and troubleshooting LC-MS/MS bioanalytical methods that support pharmaceutical clients worldwide. You will combine people leadership, scientific expertise, and client management to deliver high-quality results, drive innovation, and support the continued growth of the organization.

Job Responsibilities

Leadership & People Management

  • Lead and develop teams of bioanalytical scientists focused on LC-MS method development and validation.
  • Provide performance management, coaching, career development, and succession planning for direct reports.
  • Establish training plans and ensure team readiness for current and future business needs.
  • Lead recruitment, onboarding, and retention initiatives for scientific staff.
  • Foster a collaborative, accountable, and inclusive team culture.

Scientific & Technical Leadership

  • Serve as a subject matter expert in LC-MS/MS bioanalysis.
  • Provide technical guidance for method development, method transfer, troubleshooting, validation, and sample analysis activities.
  • Support internal teams and clients through scientific consultation and problem-solving.
  • Stay current with emerging bioanalytical technologies, regulatory expectations, and industry best practices.
  • Partner with commercial and project teams on study strategy, feasibility assessments, and client interactions.

Operational Excellence

  • Ensure laboratory activities are appropriately resourced, scheduled, and executed to meet client timelines.
  • Monitor departmental metrics and drive continuous improvement initiatives.
  • Support forecasting, project costing, and revenue recognition activities.
  • Ensure compliance with GLP, GCP, SOPs, quality standards, and safety requirements.
  • Lead corrective and preventive actions as needed to address operational or client concerns.

Client Engagement

  • Build and maintain strong relationships with pharmaceutical clients.
  • Participate in sponsor meetings, scientific discussions, and business development activities.
  • Represent the organization at scientific conferences and industry events.
Qualifications

Minimum Requirements

  • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • Significant experience, 5 years or more in regulated LC-MS bioanalysis, including method development and validation.
  • 5 years or more of demonstrated success leading scientific teams in a regulated laboratory environment.
  • 3 years or more experience working in a GLP, GCP, and bioanalytical regulatory requirements role.

Preferred Qualifications

  • Advanced degree (MS or PhD) in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • 6 years or more of experience managing people leaders in larger scientific organizations.
  • 5 years or more previous client-facing experience within a CRO or pharmaceutical setting.
  • 6 years or more experience driving operational improvements, business metrics, and laboratory productivity initiatives.
  • Documented scientific publications, conference presentations, or recognized technical expertise in bioanalysis.

Additional Job Skills

  • Excellent communication, interpersonal, and organizational skills.
  • GLP/GCP and bioanalytical regulatory requirements experience.

Why Join Us?

  • Lead a highly skilled team of bioanalytical scientists.
  • Influence strategy, innovation, and business growth.
  • Work with cutting-edge LC-MS technologies supporting drug development programs.
  • Engage with global clients and industry leaders.
  • Enjoy comprehensive benefits, professional development opportunities, and a collaborative culture focused on scientific excellence.

Salary: $130,000 – 160,000 annually

All job offers will…

Position Requirements
10+ Years work experience
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