Manager/Senior Manager, GMP Quality -...

About the role

Ionis is seeking an experienced Manager/Senior Manager, GMP Quality - Drug Substance to provide Quality Assurance activities supporting both clinical and commercial Drug Substance (DS) manufacturing and testing. This role provides strategic leadership, operational oversight, and hands-on QA expertise across internal operations and external manufacturing partners. WORK LOCATION: Onsite in Carlsbad, CA

Responsibilities

• Lead and manage GMP Quality Assurance activities supporting internal and external Drug Substance and Intermediate manufacturing, testing, and release.
• Senior Manager: May manage, mentor, and develop QA staff and/or provide functional leadership to matrixed teams, depending on organizational needs.
• Provide QA oversight across clinical and commercial programs, ensuring phase-appropriate compliance and inspection readiness.
• Oversee, and/or support and execute core Quality Management System (QMS) processes, including batch record review, deviations, investigations, CAPAs, change control, OOS/OOT management, risk management, validation, and training compliance.
• Serve as the Quality assurance interface for contract manufacturing and testing organizations (CMOs), including review and approval of manufacturing documentation, analytical data, deviations, changes, and validation packages.
• Support and/or participate in real-time QA decision-making during critical manufacturing operations.
• Support and lead regulatory inspections, partner audits, and Qualified Person (QP) interactions.
• Review and approve technical and quality documentation, including validation reports, stability data, and APQR/QMR inputs.
• Utilize enterprise quality systems, including SAP and Veeva, to support compliant and efficient quality operations.
• Support continuous improvement initiatives to enhance compliance, efficiency, and product quality.
• Collaborate cross-functionally with Technical Operations, CMC, Regulatory, Clinical, Supply Chain, and IT teams.
• Communicate quality- or supply-impacting issues clearly to internal and external stakeholders.
• Support new quality initiatives and cross-functional projects
• Apply strong cGMP knowledge in daily activities
• Perform additional duties as assigned

Requirements

• Bachelor's degree in Chemistry, Biological Sciences, Engineering, or a related discipline
• At least 5 years of pharmaceutical industry experience, including experience in Quality Assurance within a cGMP environment.
• Demonstrated experience supporting Drug Substance manufacturing across both clinical; limited commercial experience is a plus but not required.
• Experience working with CMOs/CDMOs, including oversight of manufacturing, testing, and release activities
• knowledge of global cGMP regulations (FDA, EMA, ICH, etc.).
• SAP and Veeva systems experience
• Strong analytical, technical, and critical-thinking skills.
• Excellent written and verbal communication skills.
• Ability to manage multiple priorities and adapt to changing business needs.

Pay

• The pay scale for this position is $70,844 to $126,585
• The pay scale for the Manager position is $70,844 to $102,371
• The pay scale for the Senior Manager position is $87,530 to $126,585