Job ID: JOB_ID_6906
Job Summary
We are seeking an experienced SAP Production Planning (PP) Consultant with strong domain expertise in the pharmaceutical / life sciences industry. The ideal candidate will be responsible for designing, implementing, and supporting SAP PP solutions aligned with GMP, regulatory compliance, and batch manufacturing processes.
Key Responsibilities
- Design, configure, and support SAP PP (Production Planning) solutions in S/4HANA or ECC environments
- Work closely with business stakeholders to gather requirements and translate them into functional specifications
- Configure and support: Material Requirements Planning (MRP), Bill of Materials (BOM), Routing and Work Centers, Production Orders / Process Orders
- Support batch manufacturing and process industry scenarios (PP-PI preferred)
- Integrate SAP PP with other modules: MM (Materials Management), QM (Quality Management), SD (Sales & Distribution), EWM / WM
- Ensure compliance with pharma regulations such as: GMP (Good Manufacturing Practices), FDA 21 CFR Part 11, Validation and audit requirements
- Participate in CSV (Computer System Validation) activities: IQ/OQ/PQ documentation, Test script creation and execution
- Support batch management, serialization, and traceability requirements
- Troubleshoot production planning and execution issues
- Provide end-user training and documentation
- Support cutover, data migration, and go-live activities
Required Qualifications
- Bachelors degree in Engineering, Supply Chain, IT, or related field
- 15+ years of SAP PP experience (S/4HANA preferred)
- Strong experience in pharmaceutical / life sciences manufacturing
- Hands-on experience in: Process orders, Batch management
- Knowledge of regulated environments and compliance requirements
- Familiarity with MES systems integration
- Experience with SAP PP-PI (Process Industries)
- Knowledge of: SAP QM integration (quality inspection, batch release)
Key Skills
- Strong understanding of end-to-end supply chain processes
- Excellent problem-solving and analytical skills
- Ability to work with cross-functional teams
- Strong communication and stakeholder management
- Experience in Agile / hybrid SAP project environments
Special Requirements
Hybrid/Onsite, based on project needs. Can try for Remote. Ability to support global teams across time zones. GMP, FDA 21 CFR Part 11, Validation and audit requirements, CSV (IQ/OQ/PQ), MES systems integration.
Compensation & Location
Salary: $120,000 – $160,000 per year (Estimated)
Location: Raritan, NJ
Recruiter / Company – Contact Information
Recruiter / Employer: Paramount Software Solutions Inc
Email: swarna@paramountsoft.net
Recruiter Notice:
To remove this job posting, please send an email from
swarna@paramountsoft.net with the subject:
DELETE_JOB_ID_6906