At a Glance
- Tasks: Prepare quality documentation and support product release in a dynamic team environment.
- Company: Join RoslinCT, a leader in cell and gene therapy innovation.
- Benefits: Generous salary, 31 days leave, private healthcare, and flexible benefits.
- Why this job: Make a real impact in life-changing therapies while developing your career.
- Qualifications: Degree in Life Sciences or relevant experience; strong communication skills required.
- Other info: Inclusive workplace with excellent growth opportunities and support for all applicants.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Quality Control Analyst I – DADM (Data & Documentation) – 6 Month FTC
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
- An exciting opportunity for a Quality Control Analyst I – DADM (Data & Documentation) to join our team.
- This is a temporary contract. It is anticipated that the role will be effective from Oct 2025 till Apr 2026.
- 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 documentation relating to QC activities.
- 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.
- Comply information used to communicate with clients.
- 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.
#J-18808-Ljbffr
Quality Control Analyst I – DADM (Data & Documentation) – 6 Month FTC employer: RoslinCT
Contact Detail:
RoslinCT Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Analyst I – DADM (Data & Documentation) – 6 Month FTC
✨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 the company and role thoroughly. Understand their values and how your skills align with their mission. This will help you stand out and show that you're genuinely interested in joining their team.
✨Tip Number 3
Practice common interview questions and answers with a friend or in front of a mirror. The more comfortable you are speaking about your experiences and skills, the more confident you'll feel during the actual interview.
✨Tip Number 4
Don’t forget to follow up after your interview! A simple thank-you email can leave a lasting impression and shows your enthusiasm for the position. Plus, it keeps you on their radar as they make their decision.
We think you need these skills to ace Quality Control Analyst I – DADM (Data & Documentation) – 6 Month FTC
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Control Analyst role. Highlight any relevant experience with GMP documentation and your attention to detail, as these are key for us at RoslinCT.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills align with what we’re looking for. Be genuine and let your personality come through!
Showcase Your Communication Skills: Since strong communication is vital for this position, make sure your application reflects your ability to write clearly and accurately. This will demonstrate that you can handle the documentation tasks effectively.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
How to prepare for a job interview at RoslinCT
✨Know Your GMP Documentation
Make sure you brush up on your knowledge of Good Manufacturing Practice (GMP) documentation. Familiarise yourself with the types of documents you'll be handling, like QC records and SOPs. Being able to discuss these confidently will show that you're ready for the role.
✨Showcase Your Attention to Detail
Since this role requires excellent attention to detail, prepare examples from your past experiences where your meticulousness made a difference. Whether it was in writing reports or managing documentation, having specific instances ready will highlight your suitability for the position.
✨Communicate Effectively
Strong communication skills are key for this role. Think about how you can demonstrate your ability to communicate clearly and effectively, especially when discussing complex scientific concepts. Practising your responses out loud can help you articulate your thoughts better during the interview.
✨Prepare for Team Dynamics
As you'll be working both autonomously and in teams, be ready to discuss your experience in collaborative environments. Share examples of how you've contributed to team projects or supported junior members, as this will show that you can thrive in RoslinCT's culture.