Digital Integration Lead - Italian English Speaking

Buscojobs; Sardegna; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading company is seeking a Freelance Consultant with Pharma industry experience to oversee the integration of Manufacturing Execution Systems (MES). This remote position, preferably for candidates in Italy, requires strong technical skills in MES and Automation systems as well as experience in Agile planning and cGMP standards.

Competenze

• Strong experience with MES & Automation systems.
• A thorough understanding of system cGMP requirements.
• Demonstrable knowledge of computer system design and maintenance lifecycle.

Mansioni

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

Conoscenze

Pharma Industry experience

MES & Automation systems

Technical guidance

Agile planning

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.

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