Manager, Regulatory Program Manager Immunology

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

Job Function :

Project / Program Management Group

Job Sub Function :

R&D Project Management

Job Category : Professional

All Job Posting Locations :

Allschwil Basel-Country Switzerland

Job Description :

About Innovative Medicine :

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at Immunology

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings we recommend focusing on the specific country(s) that align with your preferred location(s) :

United States - Requisition Number : R-036921

Belgium - Requisition Number : R-037688

United Kingdom - Requisition Number : R-037690

Switzerland - Requisition Number : R-037703

Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.

We are searching for the best talent for Manager Regulatory Program Manager Immunology to be located in Allschwil Switzerland. This is a hybrid position and requires you to be onsite 3 days a week.

Purpose :

The Manager Regulatory Program Manager (RPM) will be an asset-level operational leader driving projects forward through the translation and distillation of overall global regulatory strategy to executable plans and the coordination of cross-functional team efforts. This individual will serve as the primary project management point of contact to ensure Regulatory functional plans are aligned with compound / program objectives and commitments. Work closely with the Global Regulatory Leader (GRL) and partners across Global Regulatory Affairs as well as Project Management Medical Writing Clinical and other key functions to ensure confidence quality and speed in the delivery of the Johnson & Johnson Innovative Medicine (JJIM) portfolio. The Manager RPM is guided in all matters by the Johnson & Johnson Credo and held to Johnson & Johnson Leadership Performance Standards.

You will be responsible for :

• Empower teams to deliver the highest possible impact for our programs business and patients around the world.
• Translate regulatory requirements and strategy into an executable plan at a level of detail that allows teams to understand what is critical at any one time proactively identify and mitigate risks and exploit meaningful opportunities for acceleration. (e.g. MSP project plan risk and opportunity playbooks scenario evaluation and business case development).
• Lead operations with Global Regulatory Team (GRT) including activities such as ensuring visibility to and / or management of worldwide submissions driving processes to optimize global filing and launch sequencing pre and post-submission activities preparation for health authority meetings and additional major regulatory milestones.
• Provide strong operational leadership to Regulatory and program teams providing scenario and visualization support driving rapid and informed decision making challenging status quo and fostering impactful innovation.
• Support the Global Regulatory Team (GRT) in a manner that fosters and maintains a high-performance team culture facilitating GRT Submission Working Group Rapid Response Team meetings and similar as required.
• Ensure coordination of critical regulatory information and team communications to ensure timely and accurate dissemination of the GRT strategy and operational status throughout the team including co-development partners and / or other external partners as required. Liaise with Compound Development Team (CDT) and Senior Leadership Team (SLT) partners to prepare discussions and drive meeting outcomes.
• Lead the operational execution of select marketing applications including clinical variations and Pediatric submissions partnering to ensure alignment of Regulatory and compound submission strategies developing clear and detailed submission plans ensuring team roles responsibilities and accountabilities and positioning teams to proactively mitigate risks and enhance opportunities.
• Drive process improvements and embed best practices from across programs TAs and functions into supported teams.
• Work across functions and organizational boundaries to establish processes and procedures and new innovative methods that improve overall delivery.
• Build RPM value proposition through continuous refinement of delivery prioritizing and focusing on areas of highest impact and opportunity and actively leading efforts to enable enhanced capabilities and impacts.
• Serve as a mentor and coach to other RPMs and team members.
• As required work with standard budgeting and forecasting process and reporting tools to build and maintain the regulatory components and health authority budget to an overall coordinated project plan in Planisware.
• Support and facilitate activity resource and cost planning across the R&D project portfolio as required.

Qualifications / Requirements :

Preferred :

Required Skills : Preferred Skills :

Agility Jumps Business Alignment Coaching Collaborating Continuous Improvement Operational Excellence Performance Measurement Process Control Process Improvements Project Management Methodology (PMM) Project Management Office (PMO) Project Reporting Project Scheduling Quality Control (QC) Research and Development Tactical Planning Technical Credibility

Required Experience :

Manager

Key Skills

Project Management Methodology,Project / Program Management,Program Management,Management Experience,Microsoft Powerpoint,Project Management,Microsoft Project,Budgeting,DoD Experience,Leadership Experience,Supervising Experience,Contracts

Employment Type : Full-Time

Experience : years

Vacancy : 1