RoslinCT

Senior QC Analyst - Analytical 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. Find out more about what we do here ! 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 for a Senior QC Analyst - Analytical to join our Quality team. You'll be responsible for working with the development team on analytical assays for testing human embryonic stem cell lines and cell & gene therapies for human application. Identify area of improvement and lead process improvement projects within the department. Perform assimilation, statistical analysis, and interpretation of complex, multi-format data sets. Author, revise, and implement QC SOPs in alignment with regulatory guidelines. Lead root cause investigations into contamination events and deviations. Compile and report on analytical data to facilitate product release. Develop and deliver trend analyses and periodic summary reports for senior management, including QPs, and chair formal review meetings to drive data-driven improvements. Execute GMP documentation workflows within QC, including Incident Reports, Change Controls and Risk Assessments. Coordinate and perform QC batch release testing of advanced cellular therapy product Oversee day-to-day laboratory operations, ensuring adherence to cGMP, maintenance of QC systems, and operational excellence. About you Prior experience working in a GMP Quality Control molecular biology / analytical laboratory, with commercial experience. Experience in assay validation, stability testing, tissue culture, QC product testing and writing procedures to meet GMP and ICH guidelines. Experience in a variety of laboratory activities, with specialist knowledge of Flow Cytometry. Working knowledge of UK laws and regulations for cell therapy products and tissue donation. Excellent verbal communication skills, with the ability to effectively manage and influence stakeholders' and customer expectations. Exceptional written communication skills, with a good standard of written English to support writing reports accurately and clearly. Good organisational and planning skills with the ability to multi-task in a fast-paced environment. Qualifications A degree in a life science, or relevant subject. A postgraduate qualification is desirable. 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 . We're here to assist and make things as smooth as possible for you.

A leading gene therapy organization based in Edinburgh is seeking a Manufacturing Training Expert to provide advanced training within the manufacturing environment. The ideal candidate will have a Life Science degree and experience with CASGEVY processes. Responsibilities include delivering technical training, guiding aseptic practices, and collaborating with various teams to ensure compliance. This role offers competitive benefits and the opportunity to contribute to life-changing therapies.

A leading cell and gene therapy organization in Edinburgh is seeking a Senior Quality Control Analyst in Microbiology. The role involves supporting sample flow, ensuring compliance with regulatory standards, and conducting environmental monitoring within GMP cleanroom environments. Candidates should have a degree in Microbiology, at least 4 years of experience in a GMP setting, and strong attention to detail. The organization values inclusivity and offers a competitive salary package along with several benefits.

Principal MSAT Scientist 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. Find out more about what we do here! 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. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. 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. Flexible benefits such as retail discounts and access to the Cycle2Work scheme. Your new role The Principal Manufacturing Science and Technology (MSAT) Scientist will be responsible for providing in depth technical leadership and guidance on the commercial manufacturing of CASGEVY by managing complex changes associated with scale out, life cycle management, right first time and efficient operations with directly reporting to MSAT Manager. You will have direct contact with RoslinCT's client, supporting with long term process improvements and quality investigations. Create realistic, innovative solutions to complex technical and operational challenges, analysing data and presenting recommendations to both senior and executive management. Continuously drive process improvements to embed a right first time culture, ensuring best practices, efficient methodologies, and consistent quality standards are maintained. Support the resource allocation and timeline planning of new projects or demand. Lead, manage, and develop a team of MSAT Scientists and Associate MSAT Scientists, providing mentorship, technical guidance, and performance feedback to build capability and expertise within the team. Work closely with, and facilitate technical support, to wider departments within the business. Collaborate with the Business Development team on client engagement and development of new sales proposals. Ensure that all technical transfer activities are conducted in compliance with GMP, health and safety, and other relevant regulatory standard. About you Prior team leadership experience in a GMP manufacturing environment, preferably within Commercial sterile manufacturing. Working knowledge of cGMP systems and FDA/EU regulations within cell and gene therapy manufacturing. Experience working with stem cells, cellular therapies or cell banking. Exceptional communication skills - working closely with individuals at all levels including RoslinCT employees, stakeholders and suppliers. A desire to support continuous improvement, with a right first time approach. Ability to work under pressure to meet client demands and deadlines. Due to business critical needs, this role will require flexibility on working hours when required. Qualifications A Degree in Life Sciences, or related subject. 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. E EO & Accessibility 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 . We're here to assist and make things as smooth as possible for you.

Administrator (Quality Assurance) Location: Edinburgh Bioquarter, Shawfair 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. Find out more about what we do here! 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 We are looking for 2x Administrators (Quality Assurance) to join our Batch Release and QMS teams! Prepare, issue, update, and maintain controlled documents within the quality system, ensuring compliance with internal standards and regulatory requirements. Perform document management tasks using both electronic systems (such as Q-Pulse) and paper-based filing, covering manuals, policies, procedures, forms, and logs. Maintain accurate and well organised document storage and archiving systems, ensuring records remain complete and secure. Assist with the administration and tracking of incident reports, corrective and preventive actions (CAPAs), and change control processes. Provide general administrative support to the Quality Management team and wider Quality department, including scheduling, filing, and reporting tasks. Ensure all work is carried out in line with quality management system requirements. About you This position is ideal for candidates with solid administrative experience.No science background is required - we are keen to hear from applicants from a wide variety of professional backgrounds. Highly organised and detail oriented, with strong planning skills to prioritise workload and consistently deliver results within agreed deadlines. Strong communication and interpersonal skills, with the ability to build positive working relationships. Proficient in IT systems, specifically Microsoft Word with fast and accurate typing skills. Excellent attention to detail, ensuring accuracy in all documentation, record keeping, and administrative processes. Qualifications Scottish Higher Grades in Mathematics, English and Science or equivalent qualifications or experience. 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 . We're here to assist and make things as smooth as possible for you.

A leading cell and gene therapy company in Edinburgh is seeking two Administrators (Quality Assurance) to join their Batch Release and QMS teams. This role will involve preparing and maintaining controlled documents, performing document management tasks, and providing general administrative support. Candidates from diverse professional backgrounds are encouraged to apply, as no science background is required. The ideal candidate will be highly organized, detail-oriented, and proficient in Microsoft Word, with excellent communication skills.

Manufacturing Technician Location: Edinburgh BioQuarter, Little France This role is not eligible for Skilled Worker visa sponsorship. Applicants must have the right to work in the UK at the time of application. Who are we? At RoslinCT, we manufacture advanced cell therapies that help improve and save lives. We're growing fast, and we're looking for Manufacturing Technicians to join our shift teams in our modern cleanroom facilities. This is a great fit for people from backgrounds like retail, hospitality, production, warehousing, cleaning, or trades who want to work in a clean, structured, team-based environment with great job security. Why work with us? Generous salary from day one. 31 days of annual leave + 4 public holidays. Full on-the-job training - no prior experience or degree required. Private healthcare and mental health support. Group Life Cover & pension scheme. Access to Cycle to Work, retail discounts, and more. Your new role: This is a shift-based position - you will be required to work evenings and weekends on a regular basis. Carry out regular cleaning in controlled lab and cleanroom areas. Help manage supplies and materials for production. Safely handle and dispose of waste. Accurately complete important documentation. Support experienced Biotechnologists during product manufacturing. Help move materials and samples between areas. Operate and maintain specialist equipment (training provided). About you: This position is ideal for non-graduates and those with practical work experience (this does not need to be within the Life Sciences industry) and you are interested in a stable, long-term career in Life Sciences. You enjoy practical, hands-on work. You are a team player with a strong work ethic. You can follow instructions and keep things organised. Qualifications: National 5 (or equivalent) in English and Maths is required. A science subject at National 5 would be beneficial. You don't need a science background or a degree - just the right attitude and willingness to learn. If you're a university graduate, please check our careers page for other roles that may better suit your qualifications. How to Apply Click 'Apply' to upload your CV and answer a few short questions. 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 . We're here to assist and make things as smooth as possible for you.