Senior Engineer/Consultant - MES/EBR

This role supports drug product manufacturing by creating and validating electronic batch records, ensuring seamless integration with production systems. You will contribute to the optimization of manufacturing processes through data analysis and the implementation of continuous improvement initiatives. This position is crucial for future-proofing electronic batch record systems and driving global transformations within the drug product supply chain.

Key Responsibilities:

• Generate and validate electronic batch records.
• Assist with new MES functionality implementation.
• Develop standard work for MES features.
• Track NPI/EBR metrics for continuous improvement.
• Facilitate communication between GMP operations and science groups.

Must-Have Skills:

• MES PAS|X experience
• Detail-oriented approach to translate process parameters into EBRs
• Continuous Improvement mindset

Experience in the biotechnology or pharmaceutical industry, specifically within drug product manufacturing and GMP environments, is highly preferred.