Immunology Regulatory Programs Senior Analyst

Johnson & Johnson Co.; Raritan (NJ); On-site; USD 112,000 - 181,000; Full time

Benefits offered by this job

Vacation time

401(k) plan

Healthcare benefits

Parental leave

Job summary

Johnson & Johnson is seeking a Senior Analyst, Regulatory Program Manager – Immunology as part of its Innovative Medicine portfolio. This role can be located across multiple sites in the U.S. and abroad, requiring ~4 years of relevant experience and strong PM skills.

The position emphasizes coordinating regulatory strategy with cross-functional teams, leading process improvements, and ensuring timely submissions and launch activities. Domestic travel up to 10% may be required.

Qualifications

• Bachelor’s degree required; Advanced degree preferred.
• 4+ years of industry/business experience in a Pharmaceutical/MedTech or B2B setting.
• Strong project management, planning, and visualization skills.
• Ability to translate strategy into executable actions and plans.
• Excellent verbal and written communication; execution-focused.

Responsibilities

• Serve as a key facilitator within the RPM department for visibility of the work and process quality.
• Lead change management and system rollout across RPM.
• Coordinate with Global Regulatory Team on health authority planning and submissions.
• Translate regulatory strategy into detailed executable plans; identify risks and opportunities.
• Drive process improvements and embed best practices across programs and functions.

Skills

Project management

Cross-functional collaboration

Communication skills

Strategic thinking

Problem solving

Education

Bachelor's degree

Advanced degree preferred

Tools

Veeva platform

Microsoft Project

Reporting tools

Job description

Johnson & Johnson is seeking a Senior Analyst, Regulatory Program Manager – Immunology as part of its Innovative Medicine portfolio. This role can be located across multiple sites in the U.S. and abroad, requiring ~4 years of relevant experience and strong PM skills.

The position emphasizes coordinating regulatory strategy with cross-functional teams, leading process improvements, and ensuring timely submissions and launch activities. Domestic travel up to 10% may be required.