Job Description

Quality Assurance Officer II – 12-Month Fixed Term Contract

Location: Edinburgh BioQuarter

Closing Date: COB Monday 24th August 2026

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 Officer II to join our Quality team on a temporary basis It is anticipated that the role will be effective from Sep 2026 to Sep 2027

• This is a shift-based role which will include evening and weekend work.

• You’ll be responsible for providing real-time support to all RoslinCT departments on Quality matters during core working hours and out of hours.

• Ensuring maintenance of cGMP, regulatory standards and guideline knowledge.

• Reviewing, writing and updating SOPs to ensure compliance with company policies, practices and relevant standards and guidelines.

• Reviewing and approving Quality Management records inclusive of deviations, change controls & corrective and preventive actions.

• Supporting the wider Quality Assurance Team with site wide compliance and inspection readiness activities.

• Compiling quality metrics to facilitate monitoring of the RoslinCT Quality system.

About you

• Minimal 2 years relevant industry experience.

• Fully competent in cGMP principles.

• IT proficient, particularly with MS Office & an electronic quality management system.

• Excellent communication skills, with the ability to build rapport with colleagues and relevant stakeholders.

• Accurately record and report data in a clear and accurate manner.

• Strong organisation skills, with the ability to juggle prioritising tasks.

Qualifications

• A degree in Life Sciences or related field.

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.