SAP Advanced Track and Trace for Pharmaceuticals (ATTP) Consultant

High Cliff Partners Inc.
  • ANYWHERE IN NORTH AMERICA, NJ
  • Instant Apply
8 days ago

Job Description

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.

Numbers & Facts

LocationANYWHERE IN NORTH AMERICA, NJ

Skills

  • Analysis Skillsunmatched
  • Biotech and Pharmaceuticalunmatched
  • Code of Federal Regulationsunmatched
  • Commissioningunmatched
  • Consultingunmatched
  • Documentationunmatched
  • Gap Analysisunmatched
  • Government Reportingunmatched
  • Medical Productsunmatched
  • Pallet Jackunmatched
  • Product Planningunmatched
  • Reverse Engineeringunmatched
  • SAPunmatched
  • Shipping/Receivingunmatched
  • Supply Chainunmatched

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