Senior Manager, LC-MS Bioanalysis

About the role

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.

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.

Requirements

• Minimum Requirements
  • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • 5+ years of experience in regulated LC-MS bioanalysis, including method development and validation.
  • 5+ years of demonstrated success leading scientific teams in a regulated laboratory environment.
  • 3+ years of 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 of experience managing people leaders in larger scientific organizations.
  • 5+ years of previous client-facing experience within a CRO or pharmaceutical setting.
  • 6+ years of experience driving operational improvements, business metrics, and laboratory productivity initiatives.
  • Documented scientific publications, conference presentations, or recognized technical expertise in bioanalysis.

Skills

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

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
• Employee Stock Purchase Plan

Relocation assistance available.

Pay

Salary: $130,000 – $160,000 annually. The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers.

Schedule

Monday through Friday, on-site in Madison, WI.