Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.; Latina; Remoto; USD 70.000 - 90.000; Tempo pieno

Descrizione del lavoro

A leading consulting firm is seeking a Digital Integration Lead with Pharma industry experience for a REMOTE freelance opportunity in Italy. The role involves guiding the integration of manufacturing equipment with a focus on Manufacturing Execution Systems (MES). Ideal candidates will possess strong MES and automation systems experience, and have a thorough understanding of cGMP requirements.

Competenze

• Experience in Pharma industry is a must.
• Strong experience with MES and automation systems required.
• Thorough understanding of cGMP requirements needed.

Mansioni

• Guide the integration of manufacturing equipment with MES.
• Manage MES integration roadmap and deliverables.
• Facilitate Agile planning and resolve technical issues.

Conoscenze

Agile Planning

Technical Support

Problem Solving

System Design

cGMP Knowledge

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