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.
Quality Control Technician - 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 dream role
* We are looking for a Quality Control Technician – Analytical to join our team!
* You will provide QC support for routine laboratory activities including housekeeping, maintenance of equipment, assay work as well as cGMP raw material release to produce cellular therapies and documentation management.
* Perform QC activities in accordance with cGMP.
* Perform general record keeping and maintain document organisation within QC.
* Perform trending and review of QC data.
* Assist in the receipt and release of materials for use within RoslinCT GMP facilities.
* Review SOPs and update for QC activities as required.
* Complete quality related documentation including QC records.
* Support in QC laboratory activities where required including cleaning, waste disposal and co-ordinating equipment servicing and maintenance.
* Liaise with other departments to support business requirements.
About you
* Ideally, you will have experience of working within a scientific laboratory and a knowledge of GMP is desirable.
* A good standard of written English and the ability to write accurately and clearly.
* Exceptional organisational and planning skills with the ability to multi-task in a fast-paced environment
* Excellent administration and record keeping skills and attention to detail.
* A determination to continually develop and improve standards.
* Creates a positive environment through self-awareness and social skills.
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.
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.