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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.
