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 Operator. Responsible for the execution of assigned work of in-house and contracted programmes of work for the development, transfer, or cGMP Manufacture of processes as assigned to them.

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:

• Participating in multidisciplinary teams for assigned work ensuring that allocated activities are executed in a timely manner according to schedules set and ensuring that operational, quality and Health & Safety targets are met as required by the Company.

• To execute and complete assigned programmes of work both in house and contractually in a timely manner.

• To record data and communicate results through verbal and written work.

• To ensure that all operations and procedures are performed after appropriate training; that training is maintained for performing all operations and procedures and regularly updated in job training manuals.

• To actively maintain the execution of 5S system of facility management.

• To ensure laboratory notebooks, Process Development and Production documentation is completed in a timely manner and maintained to high standards as per Company

• To form part of multidisciplinary teams working within all areas of the Operations Group.

• 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 ensure consideration for cGMP needs are met when developing processes.

Qualifications:

• Minimum HNC/HND in a science subject or equivalent and / or Degree in Biochemistry, Biotechnology, Biochemical Engineering or equivalent qualification.

• Previous practical laboratory experience is desirable.

• 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