MSAT Scientist — Commercial Cell Therapy Manufacturing

RoslinCT; City of Edinburgh; On-site; GBP 42,000 - 66,000; Full time

Job summary

RoslinCT in Edinburgh is seeking a MSAT Scientist to provide technical support to commercial manufacturing and lead process transfers, improvements, and investigations. You will be in a clean room with Manufacturing colleagues and help drive continuous improvement.

The role requires hands-on cGMP cell culture experience, collaboration with cross-functional teams, and documentation of change controls, validation protocols and batch records to support quality manufacturing.

Qualifications

• 3+ years in GMP manufacturing or process technology transfer.
• Hands-on cGMP experience with cell culture.
• Experience with iPSCs, MSCs or hESC lines preferable.
• Experience with EU/MHRA/FDA regulations.
• Experience writing process change controls, validation protocols, batch records and SOPs.

Responsibilities

• Provide technical support to ongoing commercial manufacturing.
• Work in the manufacturing clean room alongside colleagues.
• Support Clinical Manufacturing on peak demand days (CNC, Grade C, Scribe, Assistant Operator).
• Mentor and train manufacturing staff on new processes and improvements.
• Write/approve change controls, validation protocols, risk assessments, batch records and SOPs.
• Support technical investigations and out-of-spec reports for timely QMS close-out.
• Troubleshoot process excursions/out-of-trends as required.
• Participate in client discussions.

Skills

GMP manufacturing

Process technology transfer

Cell culture

Regulatory experience

Technical documentation

Problem solving

Communication

Education

Life Science degree

Job description

RoslinCT in Edinburgh is seeking a MSAT Scientist to provide technical support to commercial manufacturing and lead process transfers, improvements, and investigations. You will be in a clean room with Manufacturing colleagues and help drive continuous improvement.

The role requires hands-on cGMP cell culture experience, collaboration with cross-functional teams, and documentation of change controls, validation protocols and batch records to support quality manufacturing.