Quality Control Analyst I – DADM (Data & Documentation)

Location: Edinburgh BioQuarter, Little France

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.

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 Control Analyst I – DADM (Data & Documentation) to join our team. Please note: although this role is within QC, this is a desk‑based position, so it doesn’t involve any testing in the lab.

• Prepare and complete quality‑related documentation, including QC records, change controls, deviations, and risk assessments, in line with GMP and SOP requirements.
• Author, review, and update SOPs, forms, and other GMP documentation relating to QC activities.
• Review QC Analytical and QC Microbiology data, compile QC reports and certificates of analysis to support product release and regulatory compliance.
• Conduct general record keeping and maintain document organisation.
• Support with any departmental projects as required.
• Assist in the training and development of junior team members.
• Compile information used to communicate with clients.
• Help to identify and implement process improvements within the QC department.
• Provide out of hours cover, as required on a rotational basis, for critical equipment alarms.

About you

• Prior experience working with scientific GMP documentation in chemicals or biological life sciences laboratory.
• A good standard of written English and the ability to write accurately and clearly.
• A good working knowledge of UK laws and regulations for cell therapy products and tissue donation.
• Proficient in the use of Microsoft Office applications.
• Strong communication and interpersonal skills, with the ability to develop and maintain effective working relationships.
• Skilled in managing and influencing stakeholder and customer expectations.
• Highly organised, with the ability to prioritise and manage multiple tasks in a fast‑paced environment.
• Excellent attention to detail, ensuring accuracy and consistency in all work.

Qualifications

A Degree in Life Sciences. An equivalent qualification or relevant experience will be considered.

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.