MSAT Bioprocess Specialist

TN United Kingdom; Falkirk; On-site; GBP 40,000 - 70,000; Full time

Job summary

An established industry player in healthcare is seeking a Bioprocess Engineer/Specialist to join their Manufacturing, Science & Technology team. This exciting role is perfect for someone with strong GMP pharmaceutical manufacturing experience looking to take on new challenges. You'll be responsible for preparing GMP batch records, managing projects, and ensuring quality documentation in a fast-paced environment. With flexi-time and excellent benefits, this is a fantastic opportunity to advance your career in a supportive and innovative setting.

Benefits

Private healthcare

Enhanced pension

Bonus scheme

Flexi-time

Qualifications

• Degree in a relevant scientific discipline or equivalent industry experience.
• Proven experience in GMP pharmaceutical manufacturing and process development.

Responsibilities

• Prepare GMP batch records and review manufacturing documentation.
• Project manage the introduction of processes to manufacturing.

Skills

GMP pharmaceutical manufacturing

Process development

Project management

Technical transfer

Leadership skills

Education

Degree in relevant scientific discipline

Job description

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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
• 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