At a Glance
- Tasks: Conduct thorough investigations and ensure compliance with quality standards in a dynamic 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: Experience in GMP environments and strong technical writing skills required.
- Other info: Inclusive workplace with excellent growth opportunities and support for all applicants.
The predicted salary is between 36000 - 60000 ÂŁ 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.
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 Investigator II to join our Quality Investigations Team (QIT). You’ll be responsible for performing detailed and thorough investigations of non‑compliances by closure date including product impact and/or risk assessment, systematic RCA and identification of CAPA’s and/or CC’s, by gathering data from across the organisation. Provide oversight for the development and maintenance of quality programmes, systems, processes and procedures, ensuring compliance with internal policies and internal/external standards and guidelines. Conduct ad‑hoc self‑inspections/GEMBA walkabouts of RoslinCT cleanrooms and laboratories to determine compliance with GMP and identify areas for improvement. Compile quality metrics and evaluate trends in deviation root cause and CAPA effectiveness and present this data to Department Management, Customers and Regulatory Inspectors with a view to develop improvement initiatives. Assist in training and coaching relevant personnel to support with technical writing and investigative skills. Work closely with relevant departments to ensure timely completion and closure of Quality Management work in accordance with SOP timelines. Attend QIT meetings and represent QIT at meetings to provide appropriate feedback in respect status and progression of quality management documents.
About you: Proven experience working in a GMP regulated environment, particularly in aseptic processing, documentation and record management. Background in stem cells, gene/cellular therapies or cell banking. Experience with following SOP’s and using technical RCA and FMEA techniques. Working knowledge of MHRA, FDA, EMA PICS and ISO regulations. Strong technical writing skills, with competence in reporting and presenting internally/externally. Demonstrated leadership qualities, communication, interpersonal and motivational skills. Proficient in Microsoft Office, and ideally an electronic quality management package.
Qualifications: A degree in a Life Science subject, or equivalent qualification/experience. Minimum 3-5 years’ experience in Sterile Manufacture and/or Quality‑related role. Yellow Belt certification in Lean Six Sigma is desirable.
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.
Quality Investigator II employer: RoslinCT
Contact Detail:
RoslinCT Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Investigator II
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at RoslinCT. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for interviews by practising common questions related to quality investigations and GMP compliance. We want you to shine, so think about how your experience aligns with what they’re looking for!
✨Tip Number 3
Showcase your skills! Bring examples of your work or projects that highlight your technical writing and investigative skills. This is your chance to demonstrate how you can contribute to their mission.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the team at RoslinCT.
We think you need these skills to ace Quality Investigator II
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Investigator II role. Highlight your experience in GMP regulated environments and any relevant qualifications. We want to see how your background aligns with what we do!
Showcase Your Skills: Don’t just list your skills; demonstrate them! Use specific examples from your past work that showcase your technical writing abilities and your experience with RCA and CAPA processes. This helps us see you in action!
Be Genuine in Your Application: When filling out the application form, be yourself! Share why you’re passionate about joining RoslinCT and how you can contribute to our mission. Authenticity goes a long way in making a connection with us.
Follow Up: After submitting your application, don’t hesitate to follow up if you haven’t heard back in a week or two. It shows your enthusiasm for the role and keeps you on our radar. We love proactive candidates!
How to prepare for a job interview at RoslinCT
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and relevant regulations like MHRA, FDA, and EMA. Being able to discuss how these apply to the role will show that you're not just familiar with the terms but can also apply them in practice.
✨Prepare for Technical Questions
Expect questions about technical writing and root cause analysis techniques. Be ready to share specific examples from your past experience where you've successfully implemented these skills, especially in a GMP environment.
✨Showcase Your Collaborative Spirit
RoslinCT values teamwork, so be prepared to discuss how you've worked effectively in teams before. Share instances where you’ve collaborated with different departments to achieve quality management goals or improve processes.
✨Bring Data to the Table
Since the role involves compiling quality metrics and evaluating trends, come prepared with examples of how you've used data to drive improvements in previous roles. This could include discussing CAPA effectiveness or presenting findings to management.