Building expert teams to advance science.

About the Role 

At Rose BioSolutions, our capabilities span foundational research with human immune cells and stem cells to the complete advanced therapy manufacturing continuum. We are an established operation with a world-class team of experts, and we apply our R.O.S.E standard to every program and relationship: Reliable, Outcome driven, Scalable, and Excellent!

Our manufacturing site in Keele is offering an opportunity for a Biologics Manufacturing Assistant. Responsible for the support and maintenance of the GMP facility. Responsibilities will include: daily and campaign cleaning within the GMP facility, ensuring that operational, quality and Health & Safety targets are met as required by the Company. To ensure that all activities performed are in line with the Code of Conduct. 

Why Rose BioSolutions 

At Rose, you are not just another layer in a large organization—you are a key contributor in a nimble, high-impact team. We offer:

• Direct exposure to diverse and complex client projects across multiple modalities.

• A collaborative, low-bureaucracy environment where ideas are heard and acted upon.

• Opportunities to grow your technical expertise and take ownership of your work.

• Close interaction with leadership and clients, enabling real influence on project outcomes.

Key Responsibilities:  

• Maintenance of the GMP facility, including daily and campaign cleaning. 

• Compliant completion of GMP documentation. 

• Materials preparation and autoclaving for GMP contracts. 

• Responsibility for performing autoclave performance testing. 

• Materials and equipment transfer as part of project start-up activities. 

• Responsibility for the management of small equipment calibration/re-calibration. 

• Working flexibly to support the teams delivering scientific processes within the GMP facility. 

• To perform manufacturing operations within the appropriate current Good Manufacturing Practice (cGMP) standards, ensuring compliance is maintained, as defined in the Company Quality system.  

• To adhere to proper compliance with Health and Safety of all operations within the team, in accordance with the Health, Safety, and Environmental policies and procedures. 

• To work within the company’s policies for timesheet allocation codes for assigned programmes of work and in-house activities. 

• Perform other duties that, from time to time, management will assign.  

Qualifications:

• Education: Minimum 5+ GCSE grade A-C including English Language and Mathematics or equivalent qualification.  

• Experience: Previous practical laboratory experience is desirable. 

• Other: Able to demonstrate strong written, verbal communication skills and practical skills. A self-starter, who shows initiative and is a team player. Able to work flexibly.  

Why Join Us? 

• Impact: Every process we design is a step toward a cure. You’ll be making a real impact on the health of people in your community and across the globe. 

• Expertise: Work alongside a world-class team of scientists and operational leaders in a "no-ego" environment. 

• Stability & Growth: We offer the security of an established operation with the career growth opportunities of a rapidly expanding organization. 

Perks & Benefits

• Competitive base salary with performance-based bonus opportunities.

• Benefits to support and enhance your overall well-being.

• Pension scheme