Biotechnology Jobs in Manchester

Open roles
34
Salary range
£28k – £56k
Hiring companies
10
Salary on the board

£28k – £56k

Based on advertised midpoints across the 16 priced listings posted in the last 12 months. Base salary only.

By seniority
£k base
Mid
35
56
13 jobs
Senior
40
45
1 job
Live jobs

34 live roles

See all 34 roles

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

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

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, internal and external audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Walkden, Manchester, M28 3DR, United Kingdom £40,000 – £45,000 pa
On-site Permanent
AstraZeneca logo

Logistics Coordinator – Temperature-Controlled Supply (5 Month Secondment

This role involves supporting the day-to-day logistics activities for clinical studies, ensuring medicines are delivered on time and under the correct temperature conditions. You will manage temperature excursions, coordinate with logistics partners, and contribute to continuous improvement initiatives.

AstraZeneca Macclesfield, United Kingdom
On-site Contract
AstraZeneca logo

Senior Director of Operational Technology (Operations)

This role involves leading the execution of OT strategy across AstraZeneca's global manufacturing network, ensuring alignment with business priorities and improving reliability, safety, and compliance. Key responsibilities include lifecycle management, risk mitigation, capability building, and regulatory readiness.

AstraZeneca Macclesfield, United Kingdom
On-site Permanent

Workshop Engineer, Biomedical Equipment

You will be responsible for servicing and repairing advanced biomedical equipment such as infusion pumps, patient monitors, ECG machines, and body composition devices. The role involves working in a workshop setting, maintaining and repairing these devices, and taking a flexible approach to resolving complex challenges.

TRS Consulting Bolton, Manchester, M26 1HG, United Kingdom £42,000 – £47,000 pa
On-site Permanent
Pfizer logo

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also supports site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer Manchester, M1 4HD, United Kingdom
On-site Permanent

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