MES Recipe Author - GMP Pharma Digital Systems

AbbVie Inc.; Worcester (MA); On-site; USD 66,000 - 126,000; Full time

Job summary

AbbVie is seeking a results-driven MES Recipe Author to develop, validate, and maintain electronic batch records within the MES platform (POMSnet Aquila) and support change control in GMP environments. You will work within the Digital Systems organization to ensure data integrity and compliant manufacturing documentation.

The role involves configuring MBRs/EBRs, integrating MES with ERP/LIMS, and translating paper records into digital formats.

Qualifications

• Bachelor's degree in Engineering, Computer Science, or related discipline with 2+ years of relevant experience.
• Experience in MES recipe authoring or GMP-regulated manufacturing IT applications.
• Familiarity with MES platforms and ISA-88/ISA-95 standards.
• Understanding of data integrity principles and pharmaceutical regulations.

Responsibilities

• Author, configure, and verify master batch records and electronic batch records using MES platforms.
• Support system integration between MES and ERP/LIMS/automation through cross-functional teamwork.
• Translate manufacturing requirements into digital formats and maintain system documentation.
• Perform testing of new MES recipes and system changes.
• Troubleshoot MES issues and provide on-trial support during production.
• Support change management and continuous improvement initiatives.
• Follow EH&S procedures and participate in incident investigations as required.
• Build rapport with colleagues across MES team and business users.

Skills

MES recipe authoring

GMP compliance

Data integrity

IS A-88/ISA-95 knowledge

Education

Bachelor's degree in Engineering, Computer Science, or related discipline

Tools

POMSnet Aquila

PharmaSuite

Syncade

Werum PAS-X

Job description

AbbVie is seeking a results-driven MES Recipe Author to develop, validate, and maintain electronic batch records within the MES platform (POMSnet Aquila) and support change control in GMP environments. You will work within the Digital Systems organization to ensure data integrity and compliant manufacturing documentation.

The role involves configuring MBRs/EBRs, integrating MES with ERP/LIMS, and translating paper records into digital formats.