SAP Advanced Track and Trace for Pharmaceuticals (ATTP) Consultant

High Cliff Partners Inc.; New Jersey; Ibrido; USD 185.000 - 258.000; Tempo pieno

Descrizione del lavoro

High Cliff Partners Inc. seeks an experienced SAP Advanced Track and Trace for Pharmaceuticals (ATTP) Consultant for a 44-day engagement based in New Jersey. The role requires deep ATTP expertise, proven implementation experience (upgrades/S/4HANA transitions), and a track record handling customized ATTP landscapes.

The position is primarily remote with weekly travel to the client site. You will lead fit-gap analyses, drive decisions on transitions to S/4HANA/ATTP 4.0, and coordinate with the

Competenze

• Extensive SAP ATTP experience with a proven implementation record including upgrades or S/4HANA transitions.
• Direct exposure to heavily customized ATTP landscapes and reverse-engineering of undocumented processes.
• Ability to host and lead workshops with preparation and drive to defensible outcomes.

Mansioni

• Perform fit-gap analysis of extensive ATTP customizations to map to standard features.
• Assess transitions to S/4HANA/ATTP 4.0 and determine best path.
• Analyze customizations using ATC, SPDD, and SPAU extractions.
• Host and lead stakeholder workshops with preparation and clear outcomes.
• Automate reporting to DSCSA and EU FMD authorities.
• Generate and manage serial numbers for units and tracking events.
• Ensure end-to-end visibility of tracking data and verify product authenticity.
• Support adherence to 21 CFR Part 11 and EU Annex 11.

Conoscenze

SAP ATTP

Fit-gap analysis

S/4HANA transition

Workshop facilitation

Stakeholder management

Regulatory compliance

Strumenti

ATC extracts

SPDD

SPAU

Descrizione del lavoro

Our New Jersey based client is seeking an experienced SAP Advanced Track and Trace for Pharmaceuticals (ATTP) Consultant to join their project immediately and will run for 44 days with possibility of an extension. The ideal candidate should have extensive SAP ATTP experience and a proven implementation record, ideally including upgrades or S/4HANA transitions, with direct exposure to heavily customized ATTP landscapes. Technical, migration, and Manhattan integrations are handled internally should br able to analyzing existing customizations and driving the fit-gap assessment. Must work effectively with scarce or non-existent FS and TS documentation by reverse-engineering intent from code, extracts, and stakeholder input, and hosts and leads workshops with appropriate preparation and drive to reach clear, defensible outcomes. This will be a primarily remote work with travel once a week per month to the client site.

Key Responsibilities:

• Conduct a fit-gap analysis of the client's extensive custom modifications, built years ago when the client was an early co-developer of the product, to determine whether they must be preserved or can be replaced by standard features in the latest ATTP release.
• Assess each customization against three transition outcomes for S/4HANA/ATTP 4.0: (a) Revert to SAP standard. (b) Incorporate into the SAP product roadmap, with feasibility discussed with the SAP Product Team. (c) Re-implement in alignment with S/4HANA architecture.
• Independently analyze existing customizations using the available ATC, SPDD, and SPAU extracts.
• Host and lead the workshop with appropriate preparation and drive.
• Facilitate decisions and manage stakeholders, including the SAP Product Team, to reach clear, defensible outcomes.
• Automate reporting to government authorities to meet laws such as the US Drug Supply Chain Security Act (DSCSA) and the EU Falsified Medicines Directive (EU FMD).
• Generate, allocate, track, and manage unique serial numbers for individual units, bundles, cases, and pallets.
• Store tracking events (shipping, receiving, commissioning, and returns) to maintain end-to-end visibility.
• Protect patients and brand integrity by verifying product authenticity across the supply chain.
• Speed up the identification and isolation of specific batches or units during quality issues.
• Support adherence to standards such as 21 CFR Part 11 and EU Annex 11.