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Rockwell PharmaSuite MES Consultant

Comunidad de Madrid
Spain
about 1 month ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Job source
www.jobleads.com

Tech stack

Microsoft Visio GXP

Job description

We are seeking an experienced Rockwell PharmaSuite MES Consultant with expertise in Electronic Batch Records (EBR) and pharmaceutical manufacturing. The ideal candidate will configure and validate PharmaSuite EBRs, work with business SMEs to digitize paper batch records, support process mapping, and ensure compliance with GMP/GxP standards.

Requirements

  • Rockwell PharmaSuite
  • MES (Manufacturing Execution System)
  • Electronic Batch Records (EBR)
  • Pharmaceutical Manufacturing (Solid Oral Dose/Packaging preferred)
  • GMP, Good Documentation Practices (GDP), Good Testing Practices (GTP)
  • Validation Documentation (URS, FS, CSV)
  • Process Mapping (Microsoft Visio)
  • Go-Live & HyperCare Support

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This job is hosted externally. Click below to view the full posting and apply.

Apply on www.jobleads.com
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