Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.; Milano; 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 role. This remote position requires strong experience in Manufacturing Execution Systems (MES) and technical guidance for integration projects. The ideal candidate will have a thorough understanding of cGMP requirements and technical oversight experience in Pharma environments.

Competenze

• Strong experience with MES & Automation systems.
• Understanding of system cGMP requirements.
• Technical expertise in document preparation and coding.

Mansioni

• Provide technical guidance for MES integration.
• Manage integration pack, roadmap, and deliverables.
• Analyze and solve technical issues related to MES.

Conoscenze

Technical guidance

MES integration

cGMP requirements

Agile planning

Strumenti

Manufacturing Execution System (MES)

Automation systems

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