RoslinCT EU
Lead Manufacturing Biotechnologist - Commercial Manufacturing

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Lead Manufacturing Biotechnologist – Commercial Manufacturing
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 utilizing 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 Lead Manufacturing Biotechnologist – Commercial Manufacturing to join our team.
- You will work as part of a shift team (shifts will include evening and weekend work), providing leadership to a team of employees responsible for the manufacture of an autologous, commercially licensed, Nobel prize-winning CRISPR-Cas9, gene-edited product.
- Providing line management to a team of Manufacturing Biotechnologists & Technicians by managing employee performance and development and undertaking regular 1-2-1 meetings and formal reviews with direct reports.
- Responsible for the day-to-day coordination and decision-making in respect of the team, while escalating more complex matters to the Manufacturing Section Manager and/or Manufacturing Manager as required.
- Liaising with Manufacturing Training team ensuring development of relevant training pathways for direct reports.
- Serving as a Manufacturing point of contact for the client by providing written and oral technical/batch progress updates and other relevant information as required.
- Planning and undertaking the validation of new production processes and equipment.
- Completing quality-related documentation including batch production records, change controls, incidents/deviations, and risk assessments.
- Fostering a safety-first culture by consistently adhering to all Health and Safety policies and procedures.
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
See breakdownIt searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
About you
- Prior experience working in an aseptic sterile manufacturing environment or supporting functions.
- Experience of cell culture methods and techniques.
- Working knowledge of cGMP requirements in respect of aseptic processing, contamination control, documentation, and record management.
- Working knowledge of cGMP, PICS, and ISO regulations.
- Exceptional communication, organizational, time management, and leadership skills.
- Flexible approach to working hours: The post may also involve extended hours and/or weekend work on occasion depending on workload and schedule demands.


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Qualifications
- Life Science degree and relevant experience within a cGMP manufacturing operation.
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.
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Jessica, London
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