Title : SAP S4 HANA
Location : Remote with Travel
Candidates can apply it as remote but they need to travel to Client Location Occasionally on paid expenses
Description
Support a major S/4HANA deployment for Medical Device including procedure readiness, gap assessment, and documentation updates/creation across 2 business units, plus interdependent ecosystem systems.
Notes on Manager/Project:
- Heavy documentation program tied to S/4HANA deployment and interdependent systems
- Procedure scope includes assessment of global procedures and updates plus net-new site procedures
- Needs strong cross-functional partnering with local and global SMEs, plus ability to manage trackers, timelines, and approvals
- Bilingual capability needed for translations and site-based collaboration
- Key interdependencies include MES, Maximo, EtQ, ComplianceWire, LabVantage, Enable, Blue Yonder, JDE 9.2, Digital Line Manager, Worldwide Labeling, APO SNP, SPC, Mendix
Ideal Candidate Profile:
Ideal candidate is a senior S/4HANA business systems SME with hands-on experience supporting regulated manufacturing operations and leading documentation readiness for system deployments. They have a track record of running structured procedure assessments, performing gap analysis, and driving large-scale SOP and work instruction updates and creation in collaboration with cross-functional SMEs. They are comfortable operating in complex environments where S/4HANA impacts multiple interdependent systems such as MES, Maximo, QMS, training, labeling, and LIMS, and they can translate deployment and testing timelines into clear documentation deliverables and readiness milestones. They are highly organized, capable of building and maintaining master trackers and schedules, and experienced navigating document review and approval cycles. They communicate well with both site teams and global process owners, and they can travel to Costa Rica during key phases. Bilingual English/Spanish support is strongly preferred to enable translations and effective on-site collaboration.
Include Must Have Skills:
- Deep hands-on S/4HANA knowledge in a regulated medical device manufacturing environment (MM, PP, QM, EWM)
- Proven experience creating and updating procedures, SOPs, and work instructions at scale
- Strong gap assessment skills and ability to reconcile global vs site procedure requirements
- Experience coordinating across interdependent enterprise systems (ERP plus MES, maintenance, quality, labeling, training, LIMS)
- Strong stakeholder management with local and global SMEs
- Documentation governance, tracking, review/approval workflow discipline
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