Sr. Specialist DDIT Ops ITOT Automation Eng

Novartis; Zaragoza; Presencial; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical sector is seeking a Sr. Specialist DDIT Ops ITOT Automation Engineer to manage automation in manufacturing lines. The role involves ensuring compliance, optimizing performance, and collaborating with teams globally. Ideal candidates will have extensive experience in automation within a GMP environment and strong communication skills.

Formación

• At least 7 years of experience in IT or Automation within a GMP Pharma environment.
• Strong knowledge of automation systems, validation, and pharma regulations.

Responsabilidades

• Provide technical expertise for automation software and hardware design.
• Develop and maintain OT and computer system validation processes.
• Optimize performance, reliability, and efficiency of OT systems.

Conocimientos

Communication

Problem Solving

Leadership

Educación

Bachelor’s degree in Engineering

Bachelor’s degree in Computer Science

Herramientas

Project Management Tools

Descripción del empleo

Sr. Specialist DDIT Ops ITOT Automation Eng

Join to apply for the Sr. Specialist DDIT Ops ITOT Automation Eng role at Novartis

Summary

The Automation Engineer Specialist – RLT Manufacturing Lines will support the OT scope of RLT manufacturing lines across the RLT Network and assist in developing new lines. This role involves managing automation scope, process flows, and computer system validation for automated manufacturing lines used in radioligand therapies. The candidate will ensure smooth operation of OT scope across the network and coordinate with cross-functional teams locally and globally. Strong communication skills are essential, as the RLT Line Automation Engineer will liaise with vendors and ensure timelines and SLAs are met.

About The Role

Key Responsibilities

• Provide technical expertise for automation software and hardware design, configuration, installation, and maintenance, collaborating with relevant teams.
• Understand manufacturing process flows and automation system applications.
• Develop and maintain OT and computer system validation processes to ensure compliance with regulatory standards.
• Lead project teams, define project scopes, and complete work within timelines.
• Translate business needs into technical solutions and support complex issues with vendors.
• Optimize performance, reliability, and efficiency of OT systems on automated lines.
• Work with stakeholders to resolve automation and validation challenges.
• Stay informed on industry trends, regulations, and advancements in automation for radioligand therapy manufacturing.

Essential Requirements

• Bachelor’s degree in Engineering, Computer Science, or related field.
• At least 7 years of experience in IT or Automation within a GMP Pharma environment.
• Strong knowledge of automation systems, validation, and pharma regulations.
• Proficiency in project management tools and methodologies.
• Excellent communication, collaboration, leadership, and decision-making skills.
• Detail-oriented with strong problem-solving abilities.
• Ability to thrive in a fast-paced environment.

Desirable Requirements

• Experience with Aseptic Manufacturing.
• Knowledge of radioligand therapy manufacturing processes and equipment.
• Fluency in Italian.

Additional Information

This role can be based in Ivrea, Ljubljana, or Zaragoza. Relocation support is not provided; applicants must have accessible locations.

Why Novartis: Join a community dedicated to transforming patient lives through innovative science and collaborative effort. Learn more: https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Sign up to stay informed about future opportunities: https://talentnetwork.novartis.com/network

Benefits and Rewards: Discover how we support your growth: https://www.novartis.com/careers/benefits-rewards