Analytical Methods Lead, Lifecycle & QC

Moderna; Norwood (MA); On-site; USD 109,200 - 174,600; Full time

Benefits offered by this job

Healthcare benefits

Well-being programs

Paid time off

Job summary

Moderna seeks an experienced scientist to provide technical leadership across analytical method lifecycle management for QC laboratories, manufacturing, and CMOs. You will drive method transfers, validation, troubleshooting, and investigations to ensure compliant, robust analytical performance.

You will collaborate with Quality Control, Regulatory, and Manufacturing teams, oversee investigations, data analysis, and CAPA development, and contribute to regulatory submissions and inspections.

Qualifications

• Bachelor's or higher in analytical science with multiple years of industry experience.
• Experience supporting analytical method transfer, qualification, validation, verification, or lifecycle management in GMP environments.
• Experience authoring/reviewing technical documents (Protocols/Reports/SOPs) and data integrity knowledge.

Responsibilities

• Lead and support analytical method transfers, validations, verifications, and comparability assessments.
• Provide technical expertise for method performance monitoring and lifecycle management.
• Collaborate cross-functionally to ensure robust analytical performance and compliance.

Skills

Scientific problem solving

Technical leadership

Data analysis

Effective communication

Attention to detail

Multitasking

Education

Bachelor's degree in Analytical Chemistry or related

Master's degree in Analytical Chemistry or related

PhD in Analytical Chemistry or related

Tools

Chromatography

Spectroscopy

Molecular/biochemical analyses

Quality systems (GMP)

Job description

Moderna seeks an experienced scientist to provide technical leadership across analytical method lifecycle management for QC laboratories, manufacturing, and CMOs. You will drive method transfers, validation, troubleshooting, and investigations to ensure compliant, robust analytical performance.

You will collaborate with Quality Control, Regulatory, and Manufacturing teams, oversee investigations, data analysis, and CAPA development, and contribute to regulatory submissions and inspections.