SAP S/4HANA PP & QM with Pharma & GXP experience - Contract

New Era Technology

About The Position

Join New Era Technology, where People First is at the heart of everything we do. With a global team of over 4,500 professionals, we're committed to creating a workplace where everyone feels valued, empowered, and inspired to grow. Our mission is to securely connect people, places, and information with end-to-end technology solutions at scale. At New Era, you'll join a team-oriented culture that prioritizes your personal and professional development. Work alongside industry-certified experts, access continuous training, and enjoy competitive benefits. Guided by our core attributes — putting people first, embracing continuous learning, and thriving through collaboration and inclusion — we nurture our people to deliver exceptional customer service. If you want to make an impact in a supportive, growth-oriented environment, New Era is the place for you. Apply today and help us shape the future of work—together An experienced SAP PP & QM Consultant with strong expertise in SAP S/4HANA (RISE with SAP) and deep understanding of GxP-regulated pharmaceutical environments. The candidate will play a key role in delivering compliant, validated, and scalable manufacturing and quality management solutions aligned with global regulatory requirements. The consultant must have hands-on experience in Greenfield S/4HANA implementations, validation lifecycle management, and integration with regulated systems (MES, Serialization, etc.).

Requirements

12+ years SAP PP & QM experience
Minimum 2 full lifecycle greenfield S/4HANA implementations in Pharma Industry - RISE with SAP Private Cloud
Pharma or Life Sciences industry experience (mandatory)
Strong integration knowledge (PP-QM-MM-FI)
Strong knowledge of GMP / GDP warehouse practices
Strong knowledge of GAMP 5 principles
Strong knowledge of 21 CFR Part 11 requirements
Strong knowledge of Electronic records & audit trail controls
Strong knowledge of Temperature-controlled inventory handling
Strong knowledge of FEFO (First Expiry First Out) strategy
Strong knowledge of Batch traceability & genealogy
Experience in Computer System Validation (CSV)
Experience in Validation documentation (URS, FS, DS, IQ, OQ, PQ)
Experience in Risk-based validation approach
Experience in Working closely with QA & Validation teams
Experience in Supporting regulatory audits (FDA / EMA / MHRA preferred)
Experience in regulated batch manufacturing environments
Understanding of process industries
Knowledge of Fiori Apps & Role-based access
Knowledge of Embedded Analytics
Knowledge of Business Process Intelligence
Knowledge of SAP Activate methodology
Support Fit-to-Standard workshops
WRICEF identification and design
Strong stakeholder management
Experience leading design workshops
Ability to work with global QA & compliance teams
Strong documentation skills
Consulting mindset with process-oriented thinking
Greenfield Experience is Mandatory to S/4HANA
GxP validated SAP landscape
Integration with serialization and compliance systems

Nice To Haves

Configure and implement Stability Studies (preferred)
Strong knowledge of Controlled substance handling (preferred)
SAP Certification in SAP S/4HANA Production Planning or Quality Management (preferred)