Biotechnology Jobs in Northampton

Open roles

197

Salary range

£26k – £516k

Hiring companies

View 197 live roles → Get an alert

Salary on the board

£26k – £516k

Based on advertised midpoints across the 49 priced listings posted in the last 12 months. Base salary only.

By seniority

£k base

Entry

3 jobs

Junior

2 jobs

Mid

16 jobs

Senior

150

9 jobs

Lead

3 jobs

Director

516

5 jobs

Live jobs

197 live roles

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Quality Manager

This role involves leading and improving the ISO 13485 Quality Management System within a medical device manufacturer producing Class IIa and IIb products. The Quality Manager will manage non-conformances, CAPAs, and returned product investigations while supporting supplier quality and leading internal and external audits. The position operates in a hands-on manufacturing environment with a focus on regulatory compliance and continuous quality improvement.

ProTech Recruitment Ltd Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £60,000 – £70,000 pa

On-site Permanent

Medical Affairs Partner - Nephrology & Rheumatology

Acts as a key medical affairs liaison for nephrology and rheumatology, translating complex scientific data into strategic initiatives and fostering relationships with healthcare experts. Supports local and global medical strategies, contributes to scientific partnerships, medical education, and insight generation. Works within a collaborative, patient-focused environment to improve healthcare outcomes.

Roche Welwyn Hatfield, United Kingdom

Hybrid Contract

Principal Data Strategy & Analytics Specialist

This role involves shaping data strategies and leading advanced analytics to support evidence generation and clinical decision-making using real-world and clinical trial data. The specialist will design analytical frameworks, drive data standardization, and collaborate with global teams to integrate complex data sources for patient impact.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Biomedical Engineer

This role involves hands-on maintenance and repair of laboratory biomedical equipment, including stainers, cover slippers, and Roche Ultra systems, alongside managing CMMS operations using Qualer. The engineer ensures regulatory compliance, supports lab staff with equipment best practices, and coordinates vendor services to maintain high equipment uptime across a site with approximately 500 machines. Key responsibilities include preventive maintenance, calibration, troubleshooting, and accurate documentation within a regulated R&D and diagnostics environment.

KEMIO Consulting LTD Babraham, Cambridgeshire, United Kingdom £40,000 – £55,000 pa

On-site Permanent

Regulatory Affairs Specialist - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives within a global medical devices company, working across European, American, and Asian regulatory standards. You will develop and implement solutions for compliance and management systems in a highly technical R&D and manufacturing environment. The position offers exposure to emerging regulated industries and complex, international projects.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £42,000 – £46,000 pa

On-site Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating submissions and ensuring compliance with global regulations. Works across cross-functional teams to address complex regulatory challenges and support continuous supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a matrix environment.

GSK Stevenage, United Kingdom €90,000 – €150,000 pa

Hybrid Permanent

Analytical Scientist

Conduct routine polymer analysis using HPLC and other analytical techniques, ensuring accurate data generation and compliance with quality standards. Support method development and verification within a regulated laboratory environment. Maintain lab operations and contribute to continuous improvement initiatives.

Reed Mk441Lq, MK44 1LQ, United Kingdom £27,500 – £33,500 pa

On-site Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable results for regulatory and research purposes. Working closely with statisticians and data scientists, the role involves developing validated datasets, tables, listings, and figures using CDISC standards such as SDTM and ADaM, while ensuring compliance with GxP and ICH guidelines. The position supports agile delivery within a hybrid work environment and emphasizes technical excellence, collaboration, and innovation in clinical data programming.

GSK Stevenage, United Kingdom

Hybrid Permanent

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