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For Companies At a Glance
- Tasks: Lead a team in manufacturing groundbreaking gene-edited products and ensure quality control.
- Company: Join RoslinCT, a pioneering company in cell and gene therapy since 2006.
- Benefits: Enjoy 31 days of leave, private healthcare, and flexible benefits like retail discounts.
- Why this job: Be part of a life-changing mission with a collaborative culture and career growth opportunities.
- Qualifications: A Life Science degree and experience in aseptic manufacturing are essential.
- Other info: Inclusivity is key; we welcome all applicants and support accessibility needs.
The predicted salary is between 36000 - 60000 £ per year.
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 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 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.
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, organisational, time management and leadership skills.
- Flexible approach to working hours: The post will involve regular weekend and evening work.
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. #J-18808-Ljbffr
Lead Manufacturing Biotechnologist – Commercial Manufacturing employer: RoslinCT
Contact Detail:
RoslinCT Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Manufacturing Biotechnologist – Commercial Manufacturing
✨Tip Number 1
Familiarise yourself with the latest advancements in cell and gene therapy, particularly CRISPR technology. Being able to discuss recent developments or breakthroughs during your interview will demonstrate your passion and knowledge in the field.
✨Tip Number 2
Network with professionals in the biotechnology sector, especially those who have experience in aseptic manufacturing environments. Attend industry conferences or webinars to make connections that could provide insights or referrals for the role.
✨Tip Number 3
Prepare to showcase your leadership skills by thinking of specific examples where you've successfully managed a team or project. Highlighting your ability to lead and develop others will be crucial for this position.
✨Tip Number 4
Understand the cGMP requirements and regulations relevant to the role. Being well-versed in these standards will not only help you in the interview but also show that you are ready to contribute effectively from day one.
We think you need these skills to ace Lead Manufacturing Biotechnologist – Commercial Manufacturing
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in aseptic sterile manufacturing and cell culture methods. Use specific examples that demonstrate your knowledge of cGMP requirements and leadership skills.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role at RoslinCT. Clearly articulate why you are interested in this position and how your background aligns with their mission of creating life-changing therapies.
Highlight Relevant Qualifications: Ensure you mention your Life Science degree and any relevant certifications or training related to cGMP manufacturing operations. This will help establish your credibility and suitability for the role.
Prepare for the Application Form: When completing the application form, be concise but thorough. Detail your motivations for applying and what makes you a strong candidate. Use clear language and avoid jargon to ensure your points are easily understood.
How to prepare for a job interview at RoslinCT
✨Understand the Company and Its Products
Before your interview, make sure to research RoslinCT thoroughly. Familiarise yourself with their groundbreaking work in cell and gene therapies, especially their CRISPR-Cas9 product. This knowledge will help you demonstrate your genuine interest in the company and its mission.
✨Highlight Relevant Experience
Be prepared to discuss your prior experience in aseptic sterile manufacturing environments. Emphasise your familiarity with cGMP requirements and any specific techniques you've used in cell culture. Tailor your examples to show how they align with the responsibilities of the Lead Manufacturing Biotechnologist role.
✨Showcase Leadership Skills
As this role involves leading a team, be ready to share examples of your leadership experience. Discuss how you've managed performance, conducted 1-2-1 meetings, and fostered a collaborative environment. Highlight your ability to motivate and develop team members.
✨Prepare for Technical Questions
Expect technical questions related to manufacturing processes, quality documentation, and safety protocols. Brush up on your knowledge of ISO regulations and contamination control. Being able to articulate your understanding of these topics will demonstrate your expertise and readiness for the role.
