Job Description

Computer Systems Validation (CSV) Specialist - 6-Month Fixed Term Contract

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

Computer Systems Validation (CSV) Specialist - Fixed Term Contract

to join our team.

This is a temporary contract. It is anticipated that the role will be effective for a period of 6 months.

Lead on CSV projects by monitoring key milestones and ensuring timely documentation to support compliance. Provide daily CSV support to all areas of the business including operation and retirement of suitable validated computer systems to align with current GXPs and SOPs. Advise and guide on best practices for the qualification and validation of IT services and systems. Ensure IT systems, products and services are delivered, installed, validated and maintained throughout their life cycle. Perform quality audits for prospective automated equipment and applications vendors. Conduct periodic evaluation of computer systems. Review and deliver CSV training. Maintain up-to-date knowledge of international regulatory requirements.

About you

You will be immediately available or on a very short notice period.

Prior experience working in a GMP environment in relation to CSV. Project-based work experience including activities such as regulatory audits, GAP analyses and risk assessments. Exceptional communication skills; ability to confidently communicate technical or complex concepts orally and in written form to technical and non-technical individuals. Able to effectively share knowledge with wider teams and management teams when necessary. Excellent attention to detail with a desire to continually develop and improve processes. Take responsibility for always setting high standards and ability to recognise impact of actions.

Qualifications

Life Science/Computer Science degree or relevant work experience.

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.