Quality Assurance Supervisor – 15-Month Fixed Term Contract
Location: Edinburgh BioQuarter
Please submit your application by Monday 18th May at 12pm. Applications received after this date may not be considered.
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 Quality Assurance Supervisor to join our team.
This is a temporary contract. It is anticipated that the role will be effective from June 2026 till Sep 2027.
You will be primarily responsible for supporting the Quality Assurance Manager to continually improve RoslinCT’s processes related to batch release activities within QA, QC and Operations and ensuring these are fully compliant with appropriate legislation.
Deliver product release targets through co-ordinating timely review of batch documentation within both QA and supporting departments.
Generate batch release metrics for MRM, PQR including generation of performance reports for the different functions.
Support the Qualified Person in batch record compilation and release activities.
Ensure systems are in place and are followed for the reporting and investigation of quality related incidents, defective products or adverse events and for the control of critical documents.
Assist the QA Manager with leading audit programs in all internal RoslinCT operations, and where appropriate external suppliers used in the processes of RoslinCT.
About you
GMP, regulatory and accreditation systems and compilation & release experience.
Exceptional leadership skills, with the ability to learn and share knowledge with the wider and management teams.
Competent in reporting and presenting internally / externally.
Strong decision making and analytical skills.
Effective communicator, with the ability to express this orally and in written form.
Excellent attention to detail, with the continued desire to support the development and improvement of processes.
Working knowledge in computer packages including Microsoft Office and QPulse.
Qualifications
An honours degree in a relevant Life Science discipline or equivalent qualification.
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.
