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:
1. Prepare GMP batch records for use in manufacturing processes
2. Review, approve, and issue manufacturing documentation
3. Determine scale up criteria from development to manufacturing scale
4. Generate process mass balances and flow diagrams
5. Identify, design and define large scale manufacturing equipment
6. Define materials for use in a GMP manufacturing environment
7. Generate quality documentation for raw materials and equipment
8. Work within the QMS and carry out investigations where required
9. Implement CAPAs and change controls
10. Project manage all aspects of the introduction of processes to manufacturing
11. Perform risk assessments
12. Evaluate process materials for suitability for use in manufacturing
Requirements:
13. Degree in a relevant scientific or technical discipline and/or relevant industry experience
14. Proven GMP pharmaceutical manufacturing or process development experience and technical knowledge and ability
15. Experience of managing projects
16. Prior experience of process scale up and technical transfer
17. Good leadership and organisational skills
18. Experience writing GMP batch records and documentation
19. Ability to work in a fast paced environment