Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.; Lecce; Remoto; USD 100.000 - 140.000; Tempo pieno

Descrizione del lavoro

A leading company is seeking a Freelance Consultant with solid experience in the Pharma industry's Manufacturing Execution Systems (MES). The role involves technical guidance on MES integration with clear responsibilities in managing deliverables and ensuring compliance within cGMP environments. This position offers a remote work opportunity, preferably for candidates located in Italy.

Competenze

• Experience in Pharma Industry is required.
• Strong experience with Manufacturing Execution Systems (MES).
• Demonstrable knowledge of cGMP environments.

Mansioni

• Work with teams for technical guidance on MES integration.
• Responsible for roadmap and deliverables for MES.
• Analyze and resolve technical issues related to MES.

Conoscenze

Technical guidance

MES integration

Automation systems

Agile planning

Problem solving

Understanding of cGMP requirements

Descrizione del lavoro

REMOTE opening but prefer someone in Italy who speaks Italian

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