Digital Integration Lead

JR Italy; Milano; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading consulting company is looking for a freelance consultant to support Pharma industry MES integration. The role requires strong expertise in MES & Automation systems and a thorough understanding of cGMP requirements. This remote position is preferred for candidates located in Italy who can communicate in Italian.

Competenze

• Must have Pharma Industry experience.
• Strong experience with MES & Automation systems.
• A thorough understanding of cGMP requirements.

Mansioni

• Provide technical guidance and support in the integration of equipment for Manufacturing Execution System (MES).
• Responsible for the MES integration pack, roadmap, and deliverables.
• Analyzing and solving technical issues related to the MES integration.

Conoscenze

Pharma Industry Experience

Technical Guidance

MES & Automation Systems

Agile Planning

cGMP Requirements

Descrizione del lavoro

Social network you want to login/join with:

ADR Application Development Resources, Inc.

Location:

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

701105920330117939233710

Job Views:

2

Posted:

08.06.2025

Expiry Date:

23.07.2025

Job Description:

REMOTE opening but prefer someone in Italy who speaks Italian

Length: July 1 through Dec. 31, 2025

This is a FREELANCE Consulting opening, paid in US dollars

Must have Pharma Industry experience.

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

Responsibilities:

• 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.