MSAT Scientist - Commercial Manufacturing
RoslinCTEdinburgh, Scotland, United Kingdom
Added 20 Aug · still live
Not disclosed
Salary
Not disclosed by employer
£41,700
Going rate
Skilled Worker going rate
This role may qualify for a Skilled Worker visa
SOC 2119 is an eligible occupation, but we are only 59% sure that is the right code. RoslinCT is a licensed sponsor, so if the code fits, the role should qualify. Check the occupation eligibility rules against what the job actually involves.
This could also be SOC 2113 (Biochemists and biomedical scientists, Cell therapy process science could fit biomedical scientist if lab-based biological work dominates.) or SOC 2112 (Biological scientists, Biological scientist fits if the role centres on cell biology research rather than manufacturing support.). We read the code off the advert, so it is our best guess, not the employer's.
About the role
MSAT Scientist – Commercial Manufacturing
Location: Edinburgh BioQuarter, Technopole. As travel between sites is required for this role, the successful candidate must have a driving license.
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?
An exciting opportunity for a MSAT Scientist to join our team. You will be responsible for providing technical support to a range of cell therapy manufacturing processes including process technology transfers, process improvements, process trouble shooting and quality investigations/out of specification investigations. This role will focus on providing technical support to ongoing commercial manufacturing.
An element of the role includes the need to be present in the manufacturing clean room alongside Manufacturing colleagues. Duties involved but not limited to are:
Location: Edinburgh BioQuarter, Technopole. As travel between sites is required for this role, the successful candidate must have a driving license.
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 MSAT Scientist to join our team. You will be responsible for providing technical support to a range of cell therapy manufacturing processes including process technology transfers, process improvements, process trouble shooting and quality investigations/out of specification investigations. This role will focus on providing technical support to ongoing commercial manufacturing.
An element of the role includes the need to be present in the manufacturing clean room alongside Manufacturing colleagues. Duties involved but not limited to are:
- Supporting Clinical Manufacturing on peak demand days with specific roles including CNC Support, Grade C Support, Scribe and Assistant Operator.
- Participating in client discussions.
- Writing process change controls, validation protocols, risk assessments, batch records and other relevant documentation for both ongoing and new manufacturing processes.
- Provide specialist training to manufacturing staff supporting the introduction of new manufacturing processes, changes, and improvements.
- Support (as SME) technical investigations and out of specifications generating, reviewing, and approving technical reports to support timely close-out of QMS.
- Support the troubleshooting of process excursions/out of trends as required.
- A minimal of 3 years’ experience within GMP manufacturing and/or process technology transfer roles preferably in the Cell and Therapy industry.
- Hands-on cGMP experience with cell culture and various process manufacturing activities. Experience in working with iPSCs, MSCs or hESC lines is preferable.
- Experience in working with different cell culture platforms including closed system manufacturing process.
- Experience working to EU, MHRA and FDA regulations.
- Experience in writing technical documents such as process change controls, validation protocols, batch records and standard operating procedures.
- Excellent attention to detail, proven problem solver, self-motivated and positive with a desire to develop technically in their area of expertise.
- Can do attitude with a determination to succeed and provide solution to complex problems.
- Contributes to identifying and completing continuous improvement activities to reduce costs, increase yield and productivity for the area.
- Good organisational and planning skills with the ability to plan whilst delivering results to deadline.
- Excellent oral and written communication skills; able to explain technical or complex. concepts in a clear format to both technical and non-technical audiences.
- A degree in a Life Science discipline or relevant equivalent 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.
This description is the source posting as it read when we added it. We are not affiliated with RoslinCT, so check their own site for the current details.
Where this offer sits in the market
SOC 2119 · UK · ONS ASHE 2025 · ~36k in sampleP25 £34kP75 £54k
£29kmedian £43kgoing rate £42k£54k
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Does this job guarantee visa sponsorship?
Not necessarily. RoslinCT holds a sponsor licence, but sponsorship for a specific hire is always the employer's decision. Be upfront in your application that you'll require it.
What salary is needed for this role to be eligible?
The offer must clear both the general threshold and the SOC 2119 going rate of £41,700. New-entrant and shortage discounts can lower it.