Facilities GMP Engineer in Edinburgh

RoslinCT is a global CDMO focused on Advanced Cell and Gene Therapies. It was established in 2006, built upon the ground-breaking cloning technology of Dolly the Sheep. RoslinCT is one of the first to produce clinical-grade human pluripotent stem cells and developed the first CRISPR-edited cell therapy product for a major inherited disorder, taking it from early development to commercialization.

Facilities GMP Engineer Location: Edinburgh BioQuarter

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 – 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: An exciting opportunity to join our Facilities team as a Facilities GMP Engineer. A key role which will execute engineering procedures for the design, maintenance, qualification, validation, and calibration of lab equipment, facilities, and systems in compliance with GMP and business requirements. Responsibilities include:

• Co-ordinate facility shutdown activities on site with third-party service providers.
• Apply cGMP work practices and techniques in compliance with quality and regulatory requirements.
• Investigate appropriate follow-up of any deviations.
• Maintain clean, safe engineering areas ready for audit or inspection.
• Maintenance of engineering records, logs and documentation in a compliant manner.
• Collaborate with internal and external customers and contractors ensuring safety, quality and regulatory compliance.
• Complete and review GMP documentation.
• Identify areas for improvement to the Facilities Manager and wider business.

About you: Prior experience of equipment/facilities maintenance and calibration within a GMP regulated and total productive maintenance (TPM) led environment. Knowledge in using quality management systems relating to facilities and equipment. Working knowledge of Good Engineering Practice and process improvement tools such as Six Sigma, Lean processes and FMEA. Excellent communication and interpersonal skills with a proven track record in negotiation. Highly flexible and organised in managing short-term demands and long-term workload. Able to meet tight deadlines while managing unexpected interruptions and issues. Sets high standards and considers the broader impact of actions.

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.