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- Tasks: Join our Quality team to ensure top-notch standards in life-changing therapies.
- Company: RoslinCT, a leader in cell and gene therapy innovation.
- Benefits: Generous salary, 31 days leave, private healthcare, and flexible perks.
- Why this job: Make a real impact in a rapidly growing company that values your skills.
- Qualifications: Degree in Life Sciences and experience in GMP environments required.
- Other info: Inclusive workplace with excellent career development opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Quality Assurance Officer I
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
Due to the nature and training requirements of this role, applicants must have the legal right to work in the UK with sufficient permission to meet the needs of the position. We are unable to provide visa sponsorship for this role under Home Office restrictions.
Why join us?
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The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career.
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A generous salary package – we reward our people at the level they deserve.
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31 days of annual leave, plus 4 public holidays which increases with tenure.
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A competitive company pension scheme to help you save for the future.
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Group Life Cover – you are automatically covered for three times your basic salary to give you and your family peace of mind.
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Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us.
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Flexible benefits such as retail discounts and access to the Cycle2Work scheme.
Your new role
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An exciting opportunity for a Quality Assurance Officer to join our Quality team.
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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.
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This is a shift-based role which will include evening and weekend work.
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Reviewing Standard Operating Procedures (SOPs) to ensure compliance with company policies, practices and relevant standards and guidelines.
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Writing SOPs and updating SOPs for QA activities.
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Administering, reviewing and approving Incident Reports, Change Controls and Risk Assessments.
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Performing data review audits (Batch Production Records, Validation Documents and Development Documentation as required).
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Performing internal audits to determine compliance with GMP and identify areas for improvement.
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Issuing, reviewing and closing Corrective and Preventative Actions (CA/PAs).
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Reviewing and approving suppliers / service providers including supporting with audits of critical suppliers where required.
About you
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Experience in a similar role within a relevant industry (e.g. pharmaceutical industry / stem cell activities).
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Previous experience in a GMP environment.
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A clear understanding of GMP, regulatory and accreditation systems and quality management.
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Proven experience in the maintenance of an electronic Quality Management System.
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Have excellent influencing, communication, interpersonal and, motivational skills.
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An ability to take decisions, to analyse information in a logical manner and to prepare coherent investigative and/or technical reports.
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Competent in computer packages including Microsoft Office and an electronic quality management package.
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The candidate must be able to multitask, have excellent attention to detail and time management skills.
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Excellent administration and record keeping skills.
Qualifications
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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.
Quality Assurance Officer I employer: RoslinCT
Contact Detail:
RoslinCT Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer I
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching RoslinCT and understanding their values and mission. Tailor your answers to show how your skills align with their goals, especially in quality assurance and GMP compliance.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or family to build confidence. Focus on articulating your experience in quality management and how it relates to the role of Quality Assurance Officer.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining the RoslinCT team.
We think you need these skills to ace Quality Assurance Officer I
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance Officer role. Highlight relevant experience in GMP environments and any specific skills that match the job description. We want to see how your background aligns with what we do!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how you can contribute to our mission at RoslinCT. Keep it concise but impactful – we love a good story!
Showcase Your Skills: In your application, don’t forget to showcase your influencing and communication skills. These are key for the role, so give us examples of how you've used them in past experiences. We’re all about collaboration here!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s straightforward and ensures your application gets to the right people. Plus, it shows us you’re keen on joining our team at RoslinCT!
How to prepare for a job interview at RoslinCT
✨Know Your GMP Basics
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge before the interview. RoslinCT is looking for someone with a clear understanding of GMP, so be ready to discuss how you've applied these principles in your previous roles.
✨Showcase Your Attention to Detail
As a Quality Assurance Officer, attention to detail is crucial. Prepare examples from your past experiences where your meticulous nature helped identify issues or improve processes. This will demonstrate your fit for the role.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills and decision-making abilities. Think of situations where you had to manage supplier complaints or conduct audits, and be ready to explain your thought process.
✨Highlight Your Communication Skills
Since you'll be delivering training and collaborating with various teams, it's essential to showcase your communication skills. Prepare to discuss how you've effectively communicated quality-related topics in the past, ensuring everyone is on the same page.
