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SAP Consultant e.g. SAP EWM, SAP S4/Hana, GMP, GxP, Pharma, MS-Office

Original title: SAP Consultant e.g. SAP EWM, SAP S4/Hana, GMP, GxP, Pharma, MS-Office, etc. (m/f/d)

Randstad Professional · 60311 Frankfurt am Main, Germany · Senior

  • 60311 Frankfurt am Main, Germany
  • unbefristet
  • German

Indexed (6 days ago) · refreshed constantly

Start
04.01.2027
Duration
unbefristet
Contract
Freelance / B2B
Seniority
Senior
Reference
C01353728

Required skills

Languages: German

Job description

The role involves User Acceptance Testing (UAT) and GxP/GMP documentation for an S/4HANA re-implementation in pharmaceutical production. The consultant will also create SOPs, coordinate and conduct end-user training, and support change management.

Project overview

User Acceptance Testing (UAT): Conducting and validating end-to-end SAP processes in the test environment as part of the S/4HANA re-implementation in pharmaceutical production.

GxP / GMP Documentation: Filling out, creating, reviewing, and adapting GMP-relevant documents and evidence in a GxP-compliant manner.

SOP Creation: Supporting specialist departments and operations in the new creation and revision of Standard Operating Procedures (SOPs).

Training Coordination & Execution: Organizing and conducting training for end-users in the respective specialist areas.

Creation of Training Materials: Developing training documents, quick guides, and "one-pagers" to prepare the workforce for go-live.

Change Management / Interface: Proactively approaching specialist departments (especially Materials Management / MM) to generate enthusiasm for the new EWM system among stakeholders and to reduce reservations.

Skills

Soft Skills & Work Approach:

  • Education: Completed degree in Business Informatics, Business Administration, Engineering, or a comparable qualification.
  • SAP Experience: At least 3 years of practical experience with SAP EWM and SAP S/4HANA as a key user, application support analyst, or experienced end-user.
  • Industry Knowledge (Mandatory): Demonstrable experience in the pharmaceutical industry.
  • Regulatory Affairs: Sound practical experience in GMP / GxP regulated workflows and the creation of corresponding documentation.
  • Tool Knowledge: Proficient and confident use of common MS Office programs.
  • Languages: Fluent/negotiation-level German (at least C1) and very good English.
  • Strong communication and mediation skills combined with high persuasive power.
  • Structured, detail-oriented, and solution-focused work approach (essential for validation and GMP).
  • High resilience, adaptability, and ability to abstract.
  • Teamwork, proactivity, and coordination skills.

Project details

  • Start: 04.01.2027
  • Duration: unbefristet
  • Location: 60311 Frankfurt am Main, DE
  • Languages: German

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