Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.; Salerno; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading consultancy firm is seeking a freelance consultant specializing in Pharma to provide technical guidance for MES integration. This remote role requires strong expertise in MES and Automation systems, with a focus on managing integration tasks and liaising with teams and vendors. Ideal candidates will have prior Pharma industry experience and a deep understanding of cGMP requirements.

Competenze

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

Mansioni

• Support integration of equipment for Manufacturing Execution System (MES).
• Manage MES integration pack, roadmap, and deliverables.
• Facilitate Agile planning for MES integration.

Conoscenze

Technical guidance

MES integration

Automation systems

Agile planning

Problem solving

Descrizione del lavoro

REMOTE opening but prefer someone in Italy who speaks Italian

Length : July 1 through Dec. 31, 2025

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

Must have Pharma Industry experience.

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

Job Description :

• 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).
• 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.