Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.; Perugia; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading consulting firm is seeking a Freelance Consultant for a project in the Pharma sector. The role involves providing technical support for Manufacturing Execution System (MES) integration, requiring strong expertise in MES and automation systems. Ideal candidates should have a thorough understanding of system cGMP requirements and experience in the Pharma industry.

Competenze

• Pharma industry experience required.
• Strong experience with MES & Automation systems.
• Thorough understanding of system cGMP requirements.

Mansioni

• Provide technical guidance for integrating equipment with MES.
• Manage MES integration activities, documentation and oversight.
• Analyze and solve technical issues related to MES integration.

Conoscenze

Pharmaceutical Industry Experience

MES Systems

Automation Systems

Agile Planning

Technical Analysis

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