Manufacturing Execution System (MES) Developer in Edinburgh

Closing Date: COB Friday 14th March 2025

Location: Edinburgh BioQuarter (this is a hybrid role)

Who are we? We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting-edge therapies that change people’s lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilising ground-breaking science.

Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package with enhanced overtime options – we reward our people at the level they deserve. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover – you are automatically covered for three times your basic salary to give you and your family peace of mind. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. Flexible benefits such as retail discounts and access to the Cycle2Work scheme.

Your new role: We are looking for a Manufacturing Execution System (MES) Developer to join our team! This position is responsible for supporting our Manufacturing, Quality, and Facilities departments to:

• Design and build electronic batch records, logs, and forms
• Support change management and training in the new ways of working.
• Map data flows and help design the ‘to be’ process and recipe requirements/specifications.
• Build, test, and validate the processes/systems in the MES, alongside Manufacturing, Quality, and Facilities colleagues.
• Partner with supplier developers to set up master data and a library of unit processes.
• Work with the eBR Implementation Lead to establish Roslin ways of working and SOPs specific to the MES.
• Be the system owner for the MES, accountable for maintenance and change management and training system users.

About you: At least one years’ experience in GMP Manufacturing, preferably in the Cell and Gene therapy industry. You will have the ability to work collaboratively with other departments and demonstrate good communication skills, both written and verbal, across all levels of the business. Excellent organisational skills, with the ability to work both autonomously and with others, in a fast-paced and dynamic environment. A logical/mathematical approach to work with good problem-solving skills. Experience in business process mapping, basic coding skills, and computer system validation. Demonstrate effective communication, interpersonal, and self-motivational skills. Report writing/recording output. Excellent computer skills with experience in Microsoft Word and Excel. Excellent administration and record keeping skills. Operational experience of aseptic manufacturing is preferable.

Qualifications: A degree in a relevant technology discipline.

Next Steps: If this sounds like you, then please hit ‘Apply’ now. We will ask you to upload your CV and complete a short application form detailing why you are interested and why we should hire you.

At RoslinCT, we’re all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they’re valued and encouraged to be themselves, whether they’re our employees, customers, or partners. We take pride in being an equal opportunity employer. We treat all applicants fairly and don’t discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms. If you’ve got any specific needs or concerns regarding accessibility during the recruitment process, don’t hesitate to reach out to us at jobs@roslinct.com. We’re here to assist and make things as smooth as possible for you.