Requirements
Requires proven experience in CSV within a GMP environment and a background in leading or supervising teams. A degree in Life Sciences, Computer Science, or equivalent experience is required.
Job Description
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.
- An exciting opportunity for a Validation Supervisor I to join our Validation team.
- You’ll be responsible for supervising a small team undertaking CSV activities for the business including facilities management software and equipment software.
- Monitoring key milestones within CSV projects, ensuring the availability of documented evidence at each milestone.
- Completing, reviewing and approving quality related documentation including but not limited to validation documents, change controls, deviations and risk assessments in accordance with GMP and standard operating procedures.
- Preparing, reviewing, approving and executing of CSV documentation (e.g. plans, protocols, reports, periodic reviews)
- Contributing to the set up and execution of the validation schedule for any new facility, when required.
- Communicating procedures and CSV outcomes with clients, when required.
- Providing subject matter expertise to all areas of the business, particularly in audits.
- Proven experience in Computer System Validation within a GMP regulated environment.
- A background in supervising, influencing or leading teams.
- Exceptional attention to detail, with a determination to continually develop and improve standards.
- Demonstrable experience of project-based work, including activities such as regulatory audits, GAP analysis, risk assessments and Data Integrity Assessments.
- Flexibility and adaptability to react to rapid changes in project priorities.
- Strong communication skills, particularly around communicating with customers and service providers.
- Proficient IT skills, particularly with Microsoft Word & Excel.
- A degree in Life Sciences or Computer Science related subject, or equivalent training and experience.
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.
Education
Skills
About RoslinCT
RoslinCT is a leading global contract development and manufacturing services organization (CDMO) focused on Advanced Cell Therapies. Established in 2005 and built upon the groundbreaking technology cloning of Dolly the Sheep at the Roslin Institute in 1997, RoslinCT has harnessed cutting-edge science to advance the development of human medicines. With a remarkable heritage in the field, the company has achieved significant milestones, including being among the first in the world to produce clinical-grade human pluripotent stem cells and advancing the first CRISPR-edited stem cell-based therapy for a major disease to marketing authorization. Equipped with 22 purpose-built cGMP cell therapy processing suites in Edinburgh, Scotland, and Hopkinton, Massachusetts, RoslinCT provides innovative process and analytical development, cGMP clinical and commercial manufacturing for a range of cell types for both autologous and allogeneic processes, and cGMP iPSC cell line development, gene editing, and differentiation. With tailored CDMO solutions, RoslinCT enables partners to efficiently progress from development to commercialization and deliver life-saving Cell and Gene Therapies worldwide. Discover more about our services at www.roslinct.com.
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