Digital Integration Lead - Italian English speaking

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

Descrizione del lavoro

A leading consulting company is seeking a freelance consultant specializing in Manufacturing Execution Systems for a project in Italy. This role involves providing technical guidance for the MES integration process, managing deliverables, and liaising with engineering teams. Candidates should have strong experience in the pharmaceutical industry and a thorough understanding of cGMP requirements. Fluent Italian is preferred for local interactions.

Competenze

• Pharma industry experience is required.
• Understanding of cGMP requirements needed.
• Experience in Agile planning is a plus.

Mansioni

• Provide technical guidance for MES integration.
• Manage the MES integration roadmap and deliverables.
• Liaise with site engineering and equipment vendors.

Conoscenze

Strong experience with MES & Automation systems

Technical guidance and support

Analysis and solving of technical issues

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