Manufacturing Biotechnologist I – Clinical Projects

Manufacturing Biotechnologist I – Clinical Projects
Location: Edinburgh BioQuarter, Penicuik
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!
Due to the nature and training requirements of this role, applicants must have the legal right to work in the UK with sufficient permission to meet the needs of the position. We are unable to provide visa sponsorship for this role under the Home Office restrictions.
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 Manufacturing Biotechnologist I to join our Clinical Projects team. This hands-on position will reside within the GMP Clinical Manufacturing team but offers the opportunity to gain additional experience across all Technical Operation functions including Innovation, Process & Analytical Development and MSAT.
While this role currently operates on standard working hours, there may be a requirement to move to a shift-based working pattern in the future. Successful applicants should demonstrate a high degree of flexibility, including the ability to work extended hours on process days and undertake weekend working when required.
Responsibilities include but are not limited to:
Performing hands-on manufacture of cell banks and clinical phase drug product according to Good Manufacturing Practice (GMP) within a highly controlled cleanroom environment.
Actively contribute to the successful process technical transfer and GMP translation from laboratory to cleanroom.
Completing quality related documentation including manufacturing batch records, forms and logbooks to a high level of GDP following all relevant standard operating procedures and instructions.
Assisting with change controls, deviations and risk assessments.
Participating in the qualification, calibration and maintenance of manufacturing equipment.
About you
Educational background or experience in stem cells, cellular therapies or cell banking.
Solid understanding of a GMP cleanroom environment.
Strong communication skills, particularly with report writing and recording output.
IT Proficient, particularly with Microsoft Word & Excel.
Strong problem-solving skills with excellent attention to detail.
Flexible and enthusiastic attitude to develop next-generational therapies for patients.
Qualifications
A degree in 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.

Work arrangement
No