Digital Integration Lead - Italian English speaking

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

Descrizione del lavoro

A leading consulting firm seeks a Digital Integration Lead with Pharma Industry experience for a remote freelance position. This role involves overseeing MES integration, providing technical support, and liaising with engineering teams. Candidates must have a deep understanding of cGMP requirements and strong automation skills.

Competenze

• Strong experience with Manufacturing Execution Systems (MES) and Automation.
• Familiarity with Pharma industry cGMP requirements.
• Experience in Agile methodologies.

Mansioni

• Provide technical guidance for equipment integration.
• Manage MES integration pack and roadmap.
• Facilitate Agile planning for MES integration.
• Analyze technical issues in MES integration.

Conoscenze

MES Integration

Automation Systems

Agile Planning

Technical Guidance

Descrizione del lavoro

Title : Digital Integration Lead - Italian English speaking Pharma Industry experience REMOTE opening but prefer someone in Italy who speaks Italian Location : Italy 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