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Bespak is seeking a Process Engineer to develop, optimise, validate and maintain pharmaceutical manufacturing processes ensuring safe, efficient production. You will monitor performance, drive yield and quality improvements, and troubleshoot issues in a GMP environment.
Collaboration with Manufacturing, Engineering, QA/QC, Regulatory Affairs and Supply Chain is essential, with involvement in technology transfer, scale-up, validation and continuous improvement initiatives.
As a Process Engineer, you’ll play a key role in developing, optimising, validating and maintaining pharmaceutical manufacturing processes to ensure safe, efficient and compliant production. You’ll monitor process performance, identify opportunities to improve yield, quality and efficiency, troubleshoot manufacturing issues and support continuous improvement initiatives.
Working collaboratively with Manufacturing, Engineering, QA/QC, Regulatory Affairs and Supply Chain, you’ll help ensure processes meet GMP, health, safety, environmental and regulatory requirements.
You’ll also support process design and project delivery, including new product introductions, technology transfer, process scale-up, equipment and system design, commissioning, qualification and process validation. You’ll contribute to process safety reviews such as HAZOP, LOPA and FMEA, support change controls and CAPA, and provide engineering expertise to resolve deviations and implement sustainable improvements.
Our core values are Customer Focussed, Respectful, Collaborative, and Agile these are woven into the fabric of our business and the values we measure ourselves by.
We support a healthy work-life balance and agree flexible working arrangements where possible. We are a disability-positive employer committed to diversity and inclusion. If you require any adjustments during the recruitment process, please let our recruitment team know.
We are dedicated to our BZero sustainability roadmap (targeting SBTi net-zero) and hold ISO 14001, ISO 45001, and ISO 13485 certifications.