Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.; Rimini; Remoto; USD 60.000 - 80.000; Tempo pieno

Descrizione del lavoro

A leading company in the Pharma industry is seeking a Digital Integration Lead for a freelance consulting opportunity. The role involves providing technical guidance for Manufacturing Execution System (MES) integration, requiring strong experience with MES and automation systems, and a thorough understanding of cGMP requirements. The position offers remote work opportunities, preferring candidates based in Italy who are English and Italian speakers.

Competenze

• Strong experience with MES & Automation systems.
• Thorough understanding of system cGMP requirements.
• Demonstrable knowledge of computer system design and maintenance lifecycle.

Mansioni

• Provide technical guidance and support in MES integration.
• Responsible for the MES integration pack and deliverables.
• Analyze and resolve technical issues related to the MES integration.

Conoscenze

Technical guidance

MES integration

Agile planning

cGMP requirements

Software configuration

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 through Dec. 31, 2025

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

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

Job Description :

1. Work closely with the site team responsible for manufacturing equipment to provide technical guidance and support in the integration of equipment for Manufacturing Execution System (MES).
2. Responsible for the MES integration pack, roadmap, and deliverables. Liaise with site engineering leads and automation engineers.
3. Strong experience with MES & Automation systems.
4. Facilitate and continue regular Agile planning for MES integration.
5. Analyze and resolve technical issues related to the MES integration.
6. Manage activities of URS / FRS generation, software configuration / coding, and oversee MES software documentation practices.

A thorough understanding of system cGMP requirements and demonstrable knowledge of computer system design and maintenance lifecycle in cGMP environments is required.

1. Liaise where necessary with MES platform provider, engineering contractor, and equipment vendors on the lifecycle of document preparation, approval, coding, and delivery.