Senior Manager, LC-MS Bioanalysis

Labcorp; Madison (WI); On-site; USD 140,000 - 170,000; Full time

Benefits offered by this job

Medical, Dental, Vision coverage

401(k) with employer match

PTO / Flexible Time Off

Tuition Reimbursement

Employee Stock Purchase Plan

Job summary

Labcorp seeks a Senior Manager, LC-MS Bioanalysis in Madison, WI. The role leads bioanalytical teams focused on LC-MS method development, validation, and regulatory compliance, ensuring delivery to clients and adherence to GLP/GCP standards.

The position emphasizes leadership, strategic guidance, and cross-functional collaboration. The candidate will manage performance, mentor staff, oversee training, and drive operational excellence while staying current with industry best practices and

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• 5+ years in regulated LC-MS bioanalysis, including method development/validation.
• 5+ years leading scientific teams in a regulated lab.
• 3+ years in GLP/GCP and bioanalytical regulatory roles.

Responsibilities

• 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.

Skills

LC-MS bioanalysis

Leadership

Regulatory compliance

Team coaching

Project management

Education

Bachelor's degree in Chemistry or related

Advanced degree (MS/PhD) in Chemistry or related

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 Senior Manager, LC-MS Bioanalysis to join our team in Madison, WI!

Location: Madison, WI, On-Site

Work Schedule: Monday thru Friday

Job Responsibilities

• 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.

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.

Minimum Qualifications

• 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 Standards

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

Application Window Closes: 9/17/26

• Pay Range: $140,000 – 170,000 annually

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,

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.

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