Digital Integration Lead - Italian English speaking

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

Descrizione del lavoro

An international consulting opportunity is available to provide technical guidance for MES integration in the Pharma industry. This remote freelance role prefers candidates located in Italy with a solid background in automation systems and cGMP requirements. The project duration extends from July 1 to December 31, 2025, offering competitive compensation in US dollars. Interested candidates should send their CV in English.

Competenze

• Experience in the Pharma industry is required.
• Strong experience with MES and automation systems.
• Knowledge of software configuration and cGMP environments.

Mansioni

• Work closely with site teams for MES integration.
• Manage URS/FRS generation and software documentation.
• Analyze and solve technical issues related to MES.

Conoscenze

Knowledge of cGMP requirements

Technical guidance

MES integration

Automation systems

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