Sr. Specialist DDIT Ops ITOT Automation Eng

Sr. Specialist DDIT Ops ITOT Automation Eng

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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.

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