Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.; Taverne; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading company is looking for a Freelance Consultant with expertise in Manufacturing Execution Systems (MES) within the pharmaceutical industry. This remote role requires strong experience in MES integration, technical guidance, and Agile practices. The position is available until December 31, 2025, and preference is given to candidates in Italy who can communicate in Italian.

Competenze

• Minimum of 5 years experience in Pharma Industry.
• Experience in MES integration and automation.
• Proficiency in Agile methodologies.

Mansioni

• Provide technical guidance on MES integration and support the site team.
• Manage the MES integration pack and liaise with engineering leads.
• Analyze and solve technical issues related to MES integration.

Conoscenze

Pharma Industry experience

Strong experience with MES & Automation systems

Technical guidance

Agile planning

Problem solving

Document preparation and approval

cGMP requirements understanding

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.

J-18808-Ljbffr