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- Tasks: Join our team as a Quality Assurance Officer, ensuring compliance and quality in life-changing therapies.
- Company: RoslinCT is a leading cell and gene therapy organization dedicated to innovative science.
- Benefits: Enjoy 31 days of leave, private healthcare, flexible benefits, and a competitive salary package.
- Why this job: Be part of a rapidly expanding company that values your skills and offers career development.
- Qualifications: Degree in Life Sciences and experience in GMP environments are essential.
- Other info: We embrace inclusivity and welcome applicants from all backgrounds.
The predicted salary is between 36000 - 60000 £ per year.
Location:
Edinburgh BioQuarter
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
- As part of our business expansion, we are looking for multiple Quality Assurance Officers to join our team!
- You will work as part of a shift team and your primary role will be to support the Quality Department with all activities related to maintenance of the Quality Management System.
- Reviewing Standard Operating Procedures (SOPs) to ensure compliance with company policies, practices and relevant standards and guidelines.
- Writing SOPs and updating SOPs for QA activities.
- Administering, reviewing and approving Incident Reports, Change Controls and Risk Assessments.
- Performing data review audits (Batch Production Records, Validation Documents and Development Documentation as required).
- Performing internal audits to determine compliance with GMP and identify areas for improvement.
- Issuing, reviewing and closing Corrective and Preventative Actions (CA/PAs).
- Reviewing and approving suppliers / service providers including supporting with audits of critical suppliers where required.
About You
- Experience in a similar role within a relevant industry (e.g., pharmaceutical industry / stem cell activities).
- Previous experience in a GMP environment.
- A clear understanding of GMP, regulatory and accreditation systems and quality management.
- Proven experience in the maintenance of an electronic Quality Management System.
- Excellent influencing, communication, interpersonal and motivational skills.
- An ability to make decisions, analyse information logically, and prepare coherent investigative and/or technical reports.
- Competent in computer packages including Microsoft Office and an electronic quality management system.
- The ability to multitask, with excellent attention to detail and time management skills.
- Strong administration and record-keeping skills.
Qualifications
- Educated to degree level in a Life Sciences discipline.
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 . We’re here to assist and make things as smooth as possible for you.
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Quality Assurance Officer employer: RoslinCT
Contact Detail:
RoslinCT Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer
✨Tip Number 1
Familiarize yourself with the specific regulations and standards related to GMP in the pharmaceutical industry. This knowledge will not only help you during the interview but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Highlight any experience you have with electronic Quality Management Systems. Be prepared to discuss how you've used these systems in previous roles, as this is a key requirement for the position.
✨Tip Number 3
Showcase your ability to multitask and manage time effectively. Prepare examples from your past work where you successfully handled multiple projects or tasks simultaneously, as this is crucial for the role.
✨Tip Number 4
Demonstrate your strong communication and interpersonal skills by preparing to discuss how you've influenced teams or resolved conflicts in the past. This will be important in a collaborative environment like RoslinCT.
We think you need these skills to ace Quality Assurance Officer
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Assurance Officer position. Understand the key responsibilities and required qualifications, as this will help you tailor your application.
Tailor Your CV: Customize your CV to highlight relevant experience in quality assurance, particularly in a GMP environment. Emphasize your skills in writing SOPs, conducting audits, and maintaining quality management systems.
Craft a Compelling Application Form: When completing the application form, clearly articulate why you are interested in the role and what makes you a suitable candidate. Use specific examples from your past experiences that align with the job requirements.
Proofread Your Documents: Before submitting your application, carefully proofread your CV and application form. Check for any spelling or grammatical errors, and ensure that all information is clear and concise.
How to prepare for a job interview at RoslinCT
✨Understand GMP and Quality Management Systems
Make sure you have a solid grasp of Good Manufacturing Practices (GMP) and the Quality Management System. Be prepared to discuss your previous experiences in these areas and how they relate to the role.
✨Showcase Your Attention to Detail
As a Quality Assurance Officer, attention to detail is crucial. Prepare examples from your past work where your meticulousness led to successful outcomes or improvements in quality.
✨Prepare for Technical Questions
Expect technical questions related to SOPs, Incident Reports, and audits. Brush up on your knowledge of these processes and be ready to explain how you've handled similar tasks in the past.
✨Demonstrate Strong Communication Skills
Effective communication is key in this role. Think of instances where you successfully influenced others or worked collaboratively in a team setting, and be ready to share those stories.
