Introduction

My client is a world leading healthcare company who manufacturer many of the medicinal products you probably have in your medicine cabinet. They aim to positively impact the healthcare of billions of people and they are looking for a QC equipment validation lead to join them.

The role will off you:

• A pension contribution and full healthcare
• The opportunity to join one of the worlds leading biopharma companies
• An environment that will support your plans for career progression
• Flexible working

You will be responsible for:

• Defining and executing the site automation strategy
• Defining site automation obsolescence and upgrades strategies ensuring consistent standards in hardware and software
• Designing and executing the continuous investment plan
• System ownership for Serialization and Track and Trace systems
• Leading and initiating continuous improvement projects and programmes
• Providing technical expertise during Audits
• Ensure compliance with relevant Global Engineering Standards
• Ensure that GMP, quality, health & safety processes are adhered to

You will bring the following:

• Engineering degree to Level 8
• 10+ years of experience of working in an FMCH or GMP
• 5+ years leading a team
• Experience of delivering capital projects
• Demonstrated knowledge of engineering standards and statutory requirements for plant, machinery and workplaces
• Experience of leading and managing multi skilled technicians and support engineers in the manufacturing environment

If you want to be part of an innovative company where you can grow and expand your current knowledge, GET IN TOUCH by emailing me on isaac.murray@biotalent.com