Automation Engineer

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic & innovative medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

A Day In The Life Of An Automation Engineer

• Work and communicate effectively in a multi-disciplinary team
• Develop specifications for new and bespoke laboratory automation
• Manage vendor activities – Design build, functional specifications and factory testing.
• Execute equipment validations
• Troubleshoot equipment when problems occur across laboratory and manufacturing
• Design manufacture processes and control strategies that deliver drug product of desired attributes for clinical and commercial production using a design for manufacturing (DfM) approach
• Responsible for development of drug product unit operations with a focus on process understanding, identification of critical process parameters and process optimization.
• Lead problem solving for technical manufacturing issues, applying learnings to drive continuous improvement and enhancing standards
• Work closely with the cross functions R&D team to develop processes and improve manufacturing performance through monitoring and optimisation techniques
• Role may be shift work based

Your Experience And Qualifications

Are you?

• Educated to Degree level in engineering (or related subject) and/or with proven industry experience in GxP equipment development and validation.
• Experienced in GAMP5 application.

Do you have?

• Knowledge of equipment design and health and safety requirements.
• Experience of working to current Good Manufacturing Practice and/or Good Laboratory Practice and implementing policies and procedures in line with regulatory guidelines.
• Strong verbal and written communication; collaboration and team building skills.
• Strong emotional intelligence conducive to working with multi-disciplinary organisations.
• Good planning and organising skills & adaptable to changing priorities

If so, we'd value hearing from you!

Reports To

Brian Power,

Sr Mgr, Analytical R&D

Already Working @TEVA?

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Deadline for internal applications will close on Thursday 2nd October 2025 #TJ

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