Biotechnology Jobs in York

Open roles
46
Salary range
£30k – £130k
Hiring companies
14
Salary on the board

£30k – £130k

Based on advertised midpoints across the 19 priced listings posted in the last 12 months. Base salary only.

By seniority
£k base
Mid
30
60
16 jobs
Director
120
130
1 job
Live jobs

46 live roles

See all 46 roles
GSK logo

Technical Operations Manager

Lead technical operations at a UK pharmaceutical manufacturing site, ensuring safe, compliant, and efficient production of medicines. Provide technical leadership, resolve process and equipment issues, and drive continuous improvement in a GMP-regulated environment. Collaborate with engineering, quality, and supply chain teams to maintain operational excellence and support audit readiness.

GSK Barnard Castle, United Kingdom
On-site Permanent

Biotechnology Scientist

This role involves working with bio-reactors and micro-organisms in a lab-based environment, focusing on fermentation, cultivation, and yield optimisation. You'll design experiments, scale processes from lab to production, and apply molecular biology techniques within a growing biotech team. The position offers hands-on impact in a start-up environment with opportunities for development.

Rees Technical Leeds, West Yorkshire, United Kingdom £30,000 – £50,000 pa
On-site Permanent

Biotechnology Engineer

Design and develop bioprocesses involving bio-reactors and downstream processing techniques such as membrane filtration, centrifugation, and drying. Scale laboratory methods to pilot and industrial levels while working within a highly skilled technical team. Focus on innovation and process optimisation in a start-up biotechnology environment.

Rees Technical Leeds, West Yorkshire, United Kingdom £30,000 – £50,000 pa
On-site Permanent

Medical Device / IVD Field Engineer

This role involves providing on-site and remote technical support for Genedrive’s molecular diagnostic devices in healthcare settings. You'll troubleshoot, maintain, commission, and repair medical equipment, ensuring compliance with regulatory standards and service agreements. The position requires frequent travel across the UK and internationally, acting as a technical expert and brand ambassador.

Genedrive Manchester, United Kingdom £35,000 – £45,000 pa
Hybrid Permanent Clearance Required
GSK logo

Process Safety Engineer

This role involves providing expert process safety leadership at GSK’s Barnard Castle manufacturing site, ensuring compliance with EHS regulations and delivering process safety improvements. The engineer will lead hazard assessments, support incident investigations, and drive safe working practices across production operations, with a strong focus on regulatory standards like DSEAR and CDM. The position plays a key part in maintaining safety integrity within a high-value, regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom
On-site Permanent

Quality Engineer, Medical Devices

This role involves managing quality systems for medical devices, including creating documentation, conducting internal audits, and handling customer complaints. The engineer will ensure compliance with regulatory standards such as ISO 13485 and ISO 9001 within a leading healthcare diagnostics company. The position supports product innovation and quality assurance in a highly regulated environment.

TRS Consulting Preston, East Riding Of Yorkshire, East Riding Of Yorkshire, HU12 8SB, United Kingdom £40,000 – £50,000 pa
On-site Permanent

Quality Engineer, Medical Devices

This role involves managing quality assurance processes within the medical devices sector, including developing documentation, conducting internal audits, and resolving customer complaints. The engineer will ensure compliance with ISO standards and support regulatory requirements in a company focused on innovative diagnostic systems. The position plays a key part in maintaining quality across a product range used in healthcare laboratories.

TRS Consulting Bolton, Manchester, M26 1HG, United Kingdom £40,000 – £50,000 pa
On-site Permanent

Quality & Regulatory Associate

This role involves supporting the development and maintenance of a Quality Management System aligned with ISO13485 and FDA requirements in a growing med-tech company. The candidate will manage regulatory documentation, design controls, and quality processes, contributing to audit readiness and continuous improvement. It's a hands-on position with direct impact on product compliance and regulatory submissions.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa
Hybrid Permanent

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