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Digital Integration Lead - Italian English speaking

ADR Application Development Resources, Inc.

Verona

Remoto

EUR 50.000 - 70.000

Tempo pieno

3 giorni fa
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Descrizione del lavoro

A leading consulting firm seeks a freelance MES integration consultant. The candidate will work closely with manufacturing teams, managing technical aspects of integration in a cGMP environment. Ideal applicants have strong Pharma industry experience and agile project management skills. This remote position requires excellent technical guidance abilities and familiarity with MES and automation systems.

Competenze

  • Strong background in Pharma industry.
  • Proficiency in MES and automation technologies.
  • Experience in cGMP environments.

Mansioni

  • Provide technical guidance for equipment integration in MES.
  • Manage MES integration roadmap and deliverables.
  • Facilitate Agile planning for MES integration.

Conoscenze

Pharma Industry experience
MES integration
Automation systems
Agile planning
Technical guidance

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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