Digital Integration Lead

ADR Application Development Resources, Inc.; Napoli; Remoto; USD 100.000 - 150.000; Tempo pieno

Descrizione del lavoro

A innovative consulting opportunity in the Pharma industry for a freelance technical consultant specializing in MES integration. The role involves close collaboration with site teams and management of broader integration tasks, prioritizing compliance with cGMP standards. Ideal candidates have strong industry experience and a background in Agile methodologies.

Competenze

• Strong experience with MES & Automation systems.
• Thorough understanding of cGMP requirements and system lifecycle.
• Experience with URS/FRS generation and oversight.

Mansioni

• Provide technical guidance for MES equipment integration.
• Manage MES integration pack and deliverables.
• Analyze and resolve technical MES integration issues.

Conoscenze

Pharma Industry experience

MES integration

Automation systems

Agile planning

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