Senior Manager, LC-MS Bioanalysis
Listed on 2026-08-05
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Pharmaceutical
Regulatory Compliance Specialist, Pharmaceutical Science/ Research
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 ResponsibilitiesLeadership & 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 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…
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