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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 organisation dedicated to innovative healthcare solutions.
- Benefits: Enjoy 31 days annual 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 opportunities.
- Qualifications: Degree in Life Sciences and experience in GMP environments are essential for this role.
- Other info: We embrace inclusivity and welcome applications from everyone, ensuring a fair recruitment process.
The predicted salary is between 28800 - 43200 £ per year.
Quality Assurance Officer
Location: Edinburgh BioQuarter, 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 Quality team.
- 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.
- Have excellent influencing,communication, interpersonal and, motivational skills.
- An ability to take decisions, to analyse information in a logical manner and to prepare coherent investigative and/or technical reports.
- Competent in computer packages including Microsoft Office and an electronic quality management package.
- The candidate must be able to multitask, have excellent attention to detail and time management skills.
- Excellent 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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Contact Detail:
RoslinCT Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer
✨Tip Number 1
Familiarise yourself with the latest GMP regulations and quality management systems. Understanding these will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the pharmaceutical and biotechnology sectors. Attend industry events or join relevant online forums to connect with people who can provide insights about the company and the role.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that showcase your skills in quality assurance and compliance. Be ready to explain how you've handled challenges in a GMP environment.
✨Tip Number 4
Research RoslinCT’s recent projects and achievements. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show genuine interest in joining their team.
We think you need these skills to ace Quality Assurance Officer
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and qualifications required for the Quality Assurance Officer position. Tailor your application to highlight relevant experiences that align with these requirements.
Craft a Compelling CV: Ensure your CV is up-to-date and clearly outlines your experience in quality assurance, particularly in GMP environments. Use bullet points to make it easy to read and focus on achievements that demonstrate your skills in compliance and quality management.
Write a Strong Application Form: When completing the application form, be specific about why you are interested in working at RoslinCT. Highlight your passion for cell and gene therapy and how your background in life sciences makes you a suitable candidate.
Showcase Your Skills: In your application, emphasise your communication, analytical, and organisational skills. Provide examples of how you've successfully managed quality systems or conducted audits in previous roles to demonstrate your capability.
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 how your previous experience aligns with these standards, as they are crucial for the role.
✨Showcase Your Attention to Detail
Quality Assurance requires meticulous attention to detail. During the interview, provide examples of how you've successfully managed tasks that required precision and thoroughness, such as reviewing SOPs or conducting audits.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills and decision-making abilities. Think of past experiences where you had to handle incidents or implement corrective actions, and be ready to explain your thought process.
✨Demonstrate Strong Communication Skills
As a Quality Assurance Officer, you'll need to communicate effectively with various teams. Highlight your interpersonal skills and provide examples of how you've influenced others or resolved conflicts in a professional setting.
