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 environmentCarbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy