SRG are excited to be working with a global name in the healthcare industry to help them find a Bioprocess Engineer/Specialist within their Manufacturing, Science & Technology (MSAT) team.

This is a great opportunity for someone with strong GMP pharmaceutical manufacturing or process development experience who is ready for a new challenge.

This role offers flexi-time and excellent benefits such as private healthcare, enhanced pension and bonus scheme.

The Role:

• Prepare GMP batch records for use in manufacturing processes
• Review, approve, and issue manufacturing documentation
• Determine scale up criteria from development to manufacturing scale
• Generate process mass balances and flow diagrams
• Identify, design and define large scale manufacturing equipment
• Define materials for use in a GMP manufacturing environment
• Generate quality documentation for raw materials and equipment
• Work within the QMS and carry out investigations where required
• Implement CAPAs and change controls
• Project manage all aspects of the introduction of processes to manufacturing
• Perform risk assessments
• Evaluate process materials for suitability for use in manufacturing

Requirements:

• Degree in a relevant scientific or technical discipline and/or relevant industry experience
• Proven GMP pharmaceutical manufacturing or process development experience and technical knowledge and ability
• Experience of managing projects
• Prior experience of process scale up and technical transfer
• Good leadership and organisational skills
• Experience writing GMP batch records and documentation
• Ability to work in a fast paced environment

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.