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!

We are seeking a Scientist to join our expanding team. This is an opportunity to work in a hands-on, innovation-focused environment where your scientific expertise directly contributes to client success and patient impact.

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

• Assist in the smooth running of all current and new stability programs including protocol and report generation.

• Compliant completion of GMP documentation.

• Performing QMS documentation as required.

• Assist in the management of sample receipt and storage procedures coupled with co-ordination of QC stock times.

• Contribution to the design and implementation of process and documentation improvements.

• To assist QC Leadership team in tracking and reporting of QC metrics as required.

• Performing QC pipette verification.

• Perform QC analysis of Plasmid DNA and Viral Vectors manufactured at the Keele site (Compendial methods, HPLC, qPCR, ELISA)

• Preparation of buffers and reagents for QC analysis.

• Verify equipment performance as required for GMP activities, including stability studies.

• Performing water testing and support of the full environmental monitoring program of the GMP facility, including microbial identification.

• Report any environmental excursions, quality or compliance deficiencies promptly in accordance with standard operating procedures.

• Complete data trending activities in a timely manner

• To ensure GMP compliance is maintained, as defined in the Company Quality system, for all assigned programmes of work both contracted and routine operations.

• To provide training to less experienced staff in techniques where competency has been attained.

• To work within the Companies financial polices for purchasing and timesheet allocation codes for assigned programmes of work and in-house activities.

• To contribute to initiatives to improve the performance and efficiency of the Quality group and/or Keele site.

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

Qualifications

• Education: 5+ GCSE grade A-C including English Language and Mathematics or equivalent qualification. BSc (Science) or equivalent qualification is desirable.

• Experience: Previous practical laboratory experience in a relevant technical area in an academic or industrial environment. Previous GMP experience is desirable.

• Adaptability and a proactive, solutions-oriented mindset.

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