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Quality assurance supervisor - qms

Edinburgh
RoslinCT
Supervisor
Posted: 1 August
Offer description

RoslinCT Edinburgh, Scotland, United Kingdom


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Join to apply for the Quality Assurance Supervisor - QMS role at RoslinCT

RoslinCT Edinburgh, Scotland, United Kingdom

Join to apply for the Quality Assurance Supervisor - QMS role at RoslinCT

Location: Edinburgh BioQuarter/Shawfair, Dalkeith

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 growing Quality team! You will play a vital role in maintaining and continuously improving our Quality Management System (QMS), supporting GMP operations and ensuring regulatory compliance for cell and gene therapy manufacturing.

Key responsibilities include:

* Supporting the Quality Improvement Manager in managing and enhancing the QMS.
* Leading and delivering GMP and quality training across teams.
* Ensuring effective systems are in place for incident reporting, CAPA, and documentation control.
* Driving continuous improvement and risk management activities.
* Supporting and occasionally leading internal and external audits.
* Deputising for the QA Manager when required, including reporting to senior management on QMS performance and improvements.

What We're Looking For

* Strong experience in GMP and quality systems, ideally within biologics or advanced therapies.
* Demonstrated leadership skills, with a collaborative and proactive mindset.
* Clear communication and confident decision-making underpinned by analytical thinking.
* Hands-on experience with QMS tool (e.g. Q-Pulse) and Microsoft Office.
* Excellent attention to detail and a passion for process improvement.

Qualifications

* An honours degree in a relevant Life Science discipline or equivalent qualification is essential.

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.


Seniority level

* Seniority level

Mid-Senior level


Employment type

* Employment type

Full-time


Job function

* Job function

Quality Assurance

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