Digital Integration Lead

ADR Application Development Resources, Inc.; Ravenna; Remoto; EUR 50.000 - 70.000; Part-time

Descrizione del lavoro

A leading consulting firm seeks a Freelance MES Consultant to integrate manufacturing systems in the Pharma industry. The role involves collaboration with site teams, addressing technical issues, and ensuring compliance with cGMP standards. Ideal candidates will possess robust experience in MES and automation systems, along with a strong understanding of Pharma industry requirements.

Competenze

• Strong experience with MES & Automation systems.
• Pharma Industry experience is a must.
• Thorough understanding of cGMP requirements.

Mansioni

• Provide technical support for MES integration.
• Manage software documentation practices.
• Facilitate Agile planning for MES integration.

Conoscenze

Technical guidance

MES integration

Agile planning

Problem solving

cGMP knowledge

Descrizione del lavoro

REMOTE opening but prefer someone in Italy who speaks Italian

Length :

July 1 though Dec. 31 2025

This is a FREELANCE Consulting opening and you would be paid US dollars

Must have Pharma Industry experience.

If interested, please send your CV in English to my email address :

Job Description :

• Work closely with Site team responsible for manufacturing equipment to provide technical guidance and support in the integration of equipment for Manufacturing Execution System (MES).
• Responsible for the MES integration pack, roadmap and deliverables. Liaise with site engineering leads and automation engineers.
• Strong experience with MES & Automation systems.
• Facilitating and continuing regular Agile planning for MES integration
• Analysis and solving of technical issues related to the MES integration.
• Manage activities of URS / FRS generation, software configuration / coding and general oversight to the MES software documentation practices
• A thorough understanding of system cGMP requirements and demonstrable knowledge of computer system design and maintenance lifecycle in cGMP environments.
• Liaise where necessary with MES platform provider, engineering contractor, and equipment vendors on the lifecycle of document preparation, approval, coding, and delivery