Quality Assurance Officer – Fixed Term Contract
Location: Shawfair
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 to join our team.
- This is a temporary contract. It is anticipated that the role will be effective from August 2025 till March 2026.
- Review Standard Operating Procedures (SOPs) to ensure compliance with company policies, practices and relevant standards and guidelines.
- Writing and updating SOPs for QA activities.
- Administering, reviewing and approving Incident Reports, Change Controls and Risk Assessments.
- Performing data review audits and internal audits.
- Issuing, reviewing and closing Corrective and Preventative Actions (CA/PAs).
- Overlooking and approving suppliers / service providers including supporting with audits of critical suppliers where required.
- Compiling quality metrics to facilitate monitoring of the RoslinCT Quality System.
About you
- Prior experience in a relevant area of activity (i.e. stem cell activities).
- Clear knowledge and understanding of GMP, regulatory and accreditation systems and quality management.
- Ability to report and present internally and externally.
- Demonstrate influencing, communication, interpersonal and motivational skills.
- Proven expertise in analysing information and preparing coherent investigative and / or technical reports.
- Excellent computer skills with experience in Microsoft Word and an electronic quality management package.
- Exceptional communication skills; with the ability to explain technical terms in a clear way to technical and non-technical audiences.
Qualifications
- A degree or equivalent professional qualification in a Life Science discipline or related subject.
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 [email protected]. We’re here to assist and make things as smooth as possible for you.
