Senior Validation Officer

Senior Validation Officer

Location: 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!

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 Senior Validation Officer to join our Validation team.

• You’ll be responsible for planning, managing and executing RoslinCT validation activities to include facility and equipment validation, qualification and re-verification.

• Prepare and implement validation protocols and reports.

• Perform and manage routine qualification, calibration and maintenance of equipment when required.

• Complete and review quality related documentation, including validation documents in accordance with GMP and standard operating procedures.

• Lead on the validation of new equipment and provide guidance and assistance to team members as needed.

• Communicate procedures and results with clients, and ensure patient and client information is kept confidential at all times.

About you

• Proven experience working with a validation program in a GMP environment.

• Experience working in a sterile manufacturing facility.

• Flexible and adaptable, with the ability to respond effectively to shifting project priorities.

• Excellent communication skills, particularly engaging with customers and service providers.

• Proficient in IT, specifically with Microsoft Word & Excel.

• Ideally, you will have experience with cleanroom facilities, manufacturing and QC testing equipment. Additionally, a working knowledge of UK laws and regulations relating to cell therapy products and tissue donation would be advantageous.

Qualifications

• A degree in a Life Sciences or related subject. We will also consider candidates with equivalent training and 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.