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Tier-1 brand but niche MES/SAP pharmaceutical skillset and junior level yields moderate competition.
Strong pharma and MES-specific requirements (cGMP, EBR, SAP) limit transferability across industries.
Mandates pharma manufacturing experience, MES/SAP familiarity and cGMP compliance, so moderately strict filters.
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Design, simulate, and ensure readiness of AMPS recipes aligning with site and weekly manufacturing plans.
Handle Electronic Batch Records (EBR) preparation/revision and provide end-user support on EBR execution.
Manage SAP-AMPS interface issues, troubleshoot manufacturing execution systems, and coordinate MES projects and documentation activities.
Diploma, Graduate, or Postgraduate degree in Pharmaceutical Science or Engineering discipline.
0-3+ years experience in pharmaceutical manufacturing operations.
Work Location: On Premise (Pfizer site).
Thorough knowledge of Manufacturing Execution System (MES) and hands-on SAP experience.
Experienced with Agile Manufacturing Production Systems (AMPS) and SAP in pharmaceutical manufacturing environments.
Able to manage MES, SAP, and MLM system troubleshooting and user training effectively.
Familiar with cGMP, GDP compliance, quality management, and documentation protocols in manufacturing settings.