Description

You will create, validate, and troubleshoot electronic batch records within a biopharmaceutical manufacturing environment.

This role is on-site.

Responsibilities

• Create and edit Global Manufacturing Batch Records and Parameter Value Lists in MES and ERP systems.
• Translate process specifications into electronic source documents for production.
• Manage EBR validation for new or modified processes and troubleshoot during manufacturing.
• Perform data verification, document management, and SOP revisions to ensure quality compliance.
• Support MES implementation and projects introducing new manufacturing technologies.

Required Skills

• 5+ years of software development or manufacturing-related experience.
• Direct experience with Client-X Werum software for electronic batch records.
• Proficiency with .NET Framework.
• Background in drug product manufacturing within a biopharmaceutical setting.
• Ability to translate paper-based instructions into electronic systems.
• Strong attention to detail and a quality-based mindset.
• Ability to manage complex electronic data entry according to Standard Operating Procedures.

Preferred Skills

• Bachelor's degree in Engineering, Biological Sciences, or a related graduate field.

Key Skills

Education

Any Graduate