SAP Signavio Consultant

Role: SAP Signavio Consultant
Location: New Jersey Onsite
Duration: Long Term

Role Responsibilities

1.Process Analysis and Mapping:
Utilize SAP Signavio Process Intelligence to analyze and map medical device processes (e.g., supply chain, regulatory reporting, manufacturing workflows).
Identify bottlenecks and inefficiencies in Order-to-Cash, Procure-to-Pay, and Issue-to-Resolution processes, targeting 15 20% cycle time reductions (web:12,21).

2.S/4HANA Public Cloud Migration:
Support end-to-end SAP S/4HANA Public Cloud migrations using SAP Activate methodology, focusing on process alignment with scope items (e.g., 2T2, 4X5) (web:8).
Collaborate with J&J s IT team to configure processes in SAP Central Business Configuration.

3.GxP Compliance:
Ensure process designs and documentation meet FDA/EMA GxP requirements for medical devices (e.g., sutures, surgical staplers) (web:24).
Develop audit-ready process maps and reports using SAP Signavio Process Manager.

4.Integration:
Configure integrations with SAP BTP, SAP Ariba, and third-party systems (e.g., J&J s medical device platforms) for real-time analytics (web:9,12).
Support SAP Joule AI integration for process automation and insights (web:7).

5.Stakeholder Collaboration:
Work onsite with J&J s IT, compliance, R&D, and medical device teams in Raritan or New Brunswick, NJ, to gather requirements and drive adoption (web:13).
Conduct workshops and training sessions for up to 50 end-users on SAP Fiori dashboards and Signavio tools.

6.Reporting and Analytics:
Develop SAP Fiori dashboards for regulatory reporting and operational metrics, ensuring real-time visibility for J&J s medical device operations.
Provide process performance reports using Signavio Process Intelligence.

Required Qualifications:

Experience:
7+ years in SAP consulting, with 3+ years focused on SAP Signavio (Process Intelligence, Process Manager, Collaboration Hub).
5+ years in healthcare or pharmaceutical industries, with expertise in medical device processes (e.g., supply chain, manufacturing, regulatory reporting).
Proven experience in at least 3 SAP S/4HANA Public Cloud migrations, including process optimization and GxP compliance.

Certifications (at least two required):
SAP Signavio Process Intelligence (Professional).
SAP S/4HANA Cloud, Public Edition.
SAP Activate Project Manager.
GxP Compliance for Pharmaceuticals (preferred).

Education:
Bachelor s degree in Computer Science, Information Systems, or related field.
Master s degree (preferred).

Technical Skills:
Expertise in SAP Signavio suite (Process Intelligence, Process Manager, Collaboration Hub) for process mining and modeling (web:2,21).
Proficiency in SAP S/4HANA Public Cloud (scope items: 2T2, 4X5), SAP BTP, SAP Fiori, and SAP Ariba (web:7,8,12).
Knowledge of GxP compliance and FDA/EMA regulatory requirements (web:24).
Familiarity with SAP Joule AI for process automation (web:7).

Soft Skills:
Strong communication and stakeholder management, with experience engaging IT, compliance, and R&D teams.
Proven ability to lead workshops, training, and change management initiatives.
Agile project management skills, with experience in SAP Activate methodology.